The sensory ganglion of the COCHLEAR NERVE. The cells of the spiral ganglion send fibers peripherally to the cochlear hair cells and centrally to the COCHLEAR NUCLEI of the BRAIN STEM.
The part of the inner ear (LABYRINTH) that is concerned with hearing. It forms the anterior part of the labyrinth, as a snail-like structure that is situated almost horizontally anterior to the VESTIBULAR LABYRINTH.
The cochlear part of the 8th cranial nerve (VESTIBULOCOCHLEAR NERVE). The cochlear nerve fibers originate from neurons of the SPIRAL GANGLION and project peripherally to cochlear hair cells and centrally to the cochlear nuclei (COCHLEAR NUCLEUS) of the BRAIN STEM. They mediate the sense of hearing.
A general term for the complete loss of the ability to hear from both ears.
The spiral EPITHELIUM containing sensory AUDITORY HAIR CELLS and supporting cells in the cochlea. Organ of Corti, situated on the BASILAR MEMBRANE and overlaid by a gelatinous TECTORIAL MEMBRANE, converts sound-induced mechanical waves to neural impulses to the brain.
Computed tomography where there is continuous X-ray exposure to the patient while being transported in a spiral or helical pattern through the beam of irradiation. This provides improved three-dimensional contrast and spatial resolution compared to conventional computed tomography, where data is obtained and computed from individual sequential exposures.
Electrical waves in the CEREBRAL CORTEX generated by BRAIN STEM structures in response to auditory click stimuli. These are found to be abnormal in many patients with CEREBELLOPONTINE ANGLE lesions, MULTIPLE SCLEROSIS, or other DEMYELINATING DISEASES.
Clusters of multipolar neurons surrounded by a capsule of loosely organized CONNECTIVE TISSUE located outside the CENTRAL NERVOUS SYSTEM.
Sensory cells in the organ of Corti, characterized by their apical stereocilia (hair-like projections). The inner and outer hair cells, as defined by their proximity to the core of spongy bone (the modiolus), change morphologically along the COCHLEA. Towards the cochlear apex, the length of hair cell bodies and their apical STEREOCILIA increase, allowing differential responses to various frequencies of sound.
Cells forming a framework supporting the sensory AUDITORY HAIR CELLS in the organ of Corti. Lateral to the medial inner hair cells, there are inner pillar cells, outer pillar cells, Deiters cells, Hensens cells, Claudius cells, Boettchers cells, and others.
Gradual bilateral hearing loss associated with aging that is due to progressive degeneration of cochlear structures and central auditory pathways. Hearing loss usually begins with the high frequencies then progresses to sounds of middle and low frequencies.
Neurons of the innermost layer of the retina, the internal plexiform layer. They are of variable sizes and shapes, and their axons project via the OPTIC NERVE to the brain. A small subset of these cells act as photoreceptors with projections to the SUPRACHIASMATIC NUCLEUS, the center for regulating CIRCADIAN RHYTHM.
A neurotrophic factor involved in regulating the survival of visceral and proprioceptive sensory neurons. It is closely homologous to nerve growth factor beta and BRAIN-DERIVED NEUROTROPHIC FACTOR.
Sensory ganglia located on the dorsal spinal roots within the vertebral column. The spinal ganglion cells are pseudounipolar. The single primary branch bifurcates sending a peripheral process to carry sensory information from the periphery and a central branch which relays that information to the spinal cord or brain.
Auditory sensory cells of organ of Corti, usually placed in one row medially to the core of spongy bone (the modiolus). Inner hair cells are in fewer numbers than the OUTER AUDITORY HAIR CELLS, and their STEREOCILIA are approximately twice as thick as those of the outer hair cells.
Large subcortical nuclear masses derived from the telencephalon and located in the basal regions of the cerebral hemispheres.
Ganglia of the sympathetic nervous system including the paravertebral and the prevertebral ganglia. Among these are the sympathetic chain ganglia, the superior, middle, and inferior cervical ganglia, and the aorticorenal, celiac, and stellate ganglia.
A layer of stratified EPITHELIUM forming the endolymphatic border of the cochlear duct at the lateral wall of the cochlea. Stria vascularis contains primarily three cell types (marginal, intermediate, and basal), and capillaries. The marginal cells directly facing the ENDOLYMPH are important in producing ion gradients and endochoclear potential.
Fenestra of the cochlea, an opening in the basal wall between the MIDDLE EAR and the INNER EAR, leading to the cochlea. It is closed by a secondary tympanic membrane.
Clusters of neurons and their processes in the autonomic nervous system. In the autonomic ganglia, the preganglionic fibers from the central nervous system synapse onto the neurons whose axons are the postganglionic fibers innervating target organs. The ganglia also contain intrinsic neurons and supporting cells and preganglionic fibers passing through to other ganglia.
Electronic hearing devices typically used for patients with normal outer and middle ear function, but defective inner ear function. In the COCHLEA, the hair cells (HAIR CELLS, VESTIBULAR) may be absent or damaged but there are residual nerve fibers. The device electrically stimulates the COCHLEAR NERVE to create sound sensation.
A spiral tube that is firmly suspended in the bony shell-shaped part of the cochlea. This ENDOLYMPH-filled cochlear duct begins at the vestibule and makes 2.5 turns around a core of spongy bone (the modiolus) thus dividing the PERILYMPH-filled spiral canal into two channels, the SCALA VESTIBULI and the SCALA TYMPANI.
The ability or act of sensing and transducing ACOUSTIC STIMULATION to the CENTRAL NERVOUS SYSTEM. It is also called audition.
The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM.
A general term for the complete or partial loss of the ability to hear from one or both ears.
The semilunar-shaped ganglion containing the cells of origin of most of the sensory fibers of the trigeminal nerve. It is situated within the dural cleft on the cerebral surface of the petrous portion of the temporal bone and gives off the ophthalmic, maxillary, and part of the mandibular nerves.
A member of the nerve growth factor family of trophic factors. In the brain BDNF has a trophic action on retinal, cholinergic, and dopaminergic neurons, and in the peripheral nervous system it acts on both motor and sensory neurons. (From Kendrew, The Encyclopedia of Molecular Biology, 1994)
The essential part of the hearing organ consists of two labyrinthine compartments: the bony labyrinthine and the membranous labyrinth. The bony labyrinth is a complex of three interconnecting cavities or spaces (COCHLEA; VESTIBULAR LABYRINTH; and SEMICIRCULAR CANALS) in the TEMPORAL BONE. Within the bony labyrinth lies the membranous labyrinth which is a complex of sacs and tubules (COCHLEAR DUCT; SACCULE AND UTRICLE; and SEMICIRCULAR DUCTS) forming a continuous space enclosed by EPITHELIUM and connective tissue. These spaces are filled with LABYRINTHINE FLUIDS of various compositions.
Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
Pathological processes of the snail-like structure (COCHLEA) of the inner ear (LABYRINTH) which can involve its nervous tissue, blood vessels, or fluid (ENDOLYMPH).
The audibility limit of discriminating sound intensity and pitch.
Ganglia of the parasympathetic nervous system, including the ciliary, pterygopalatine, submandibular, and otic ganglia in the cranial region and intrinsic (terminal) ganglia associated with target organs in the thorax and abdomen.
Surgical insertion of an electronic hearing device (COCHLEAR IMPLANTS) with electrodes to the COCHLEAR NERVE in the inner ear to create sound sensation in patients with residual nerve fibers.
A spiral thickening of the fibrous lining of the cochlear wall. Spiral ligament secures the membranous COCHLEAR DUCT to the bony spiral canal of the COCHLEA. Its spiral ligament fibrocytes function in conjunction with the STRIA VASCULARIS to mediate cochlear ion homeostasis.
Clusters of neurons in the somatic peripheral nervous system which contain the cell bodies of sensory nerve axons. Sensory ganglia may also have intrinsic interneurons and non-neuronal supporting cells.
In tissue culture, hairlike projections of neurons stimulated by growth factors and other molecules. These projections may go on to form a branched tree of dendrites or a single axon or they may be reabsorbed at a later stage of development. "Neurite" may refer to any filamentous or pointed outgrowth of an embryonal or tissue-culture neural cell.
Sensory cells of organ of Corti. In mammals, they are usually arranged in three or four rows, and away from the core of spongy bone (the modiolus), lateral to the INNER AUDITORY HAIR CELLS and other supporting structures. Their cell bodies and STEREOCILIA increase in length from the cochlear base toward the apex and laterally across the rows, allowing differential responses to various frequencies of sound.
Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways.
Hearing loss due to disease of the AUDITORY PATHWAYS (in the CENTRAL NERVOUS SYSTEM) which originate in the COCHLEAR NUCLEI of the PONS and then ascend bilaterally to the MIDBRAIN, the THALAMUS, and then the AUDITORY CORTEX in the TEMPORAL LOBE. Bilateral lesions of the auditory pathways are usually required to cause central hearing loss. Cortical deafness refers to loss of hearing due to bilateral auditory cortex lesions. Unilateral BRAIN STEM lesions involving the cochlear nuclei may result in unilateral hearing loss.
Refers to animals in the period of time just after birth.
The lower chamber of the COCHLEA, extending from the round window to the helicotrema (the opening at the apex that connects the PERILYMPH-filled spaces of scala tympani and SCALA VESTIBULI).
Either of a pair of compound bones forming the lateral (left and right) surfaces and base of the skull which contains the organs of hearing. It is a large bone formed by the fusion of parts: the squamous (the flattened anterior-superior part), the tympanic (the curved anterior-inferior part), the mastoid (the irregular posterior portion), and the petrous (the part at the base of the skull).
A common name used for the genus Cavia. The most common species is Cavia porcellus which is the domesticated guinea pig used for pets and biomedical research.
Inbred CBA mice are a strain of laboratory mice that have been selectively bred to be genetically identical and uniform, which makes them useful for scientific research, particularly in the areas of immunology and cancer.
Neurons which conduct NERVE IMPULSES to the CENTRAL NERVOUS SYSTEM.
Factors which enhance the growth potentialities of sensory and sympathetic nerve cells.
A paravertebral sympathetic ganglion formed by the fusion of the inferior cervical and first thoracic ganglia.
NEURAL PATHWAYS and connections within the CENTRAL NERVOUS SYSTEM, beginning at the hair cells of the ORGAN OF CORTI, continuing along the eighth cranial nerve, and terminating at the AUDITORY CORTEX.
Abrupt changes in the membrane potential that sweep along the CELL MEMBRANE of excitable cells in response to excitation stimuli.
The inferior (caudal) ganglion of the vagus (10th cranial) nerve. The unipolar nodose ganglion cells are sensory cells with central projections to the medulla and peripheral processes traveling in various branches of the vagus nerve.
Use of sound to elicit a response in the nervous system.
The span of viability of a cell characterized by the capacity to perform certain functions such as metabolism, growth, reproduction, some form of responsiveness, and adaptability.
Neurons which send impulses peripherally to activate muscles or secretory cells.
The brain stem nucleus that receives the central input from the cochlear nerve. The cochlear nucleus is located lateral and dorsolateral to the inferior cerebellar peduncles and is functionally divided into dorsal and ventral parts. It is tonotopically organized, performs the first stage of central auditory processing, and projects (directly or indirectly) to higher auditory areas including the superior olivary nuclei, the medial geniculi, the inferior colliculi, and the auditory cortex.
Hearing loss due to exposure to explosive loud noise or chronic exposure to sound level greater than 85 dB. The hearing loss is often in the frequency range 4000-6000 hertz.
Pathological processes of the VESTIBULOCOCHLEAR NERVE, including the branches of COCHLEAR NERVE and VESTIBULAR NERVE. Common examples are VESTIBULAR NEURITIS, cochlear neuritis, and ACOUSTIC NEUROMA. Clinical signs are varying degree of HEARING LOSS; VERTIGO; and TINNITUS.
Antibiotic complex produced by Streptomyces kanamyceticus from Japanese soil. Comprises 3 components: kanamycin A, the major component, and kanamycins B and C, the minor components.
An oval, bony chamber of the inner ear, part of the bony labyrinth. It is continuous with bony COCHLEA anteriorly, and SEMICIRCULAR CANALS posteriorly. The vestibule contains two communicating sacs (utricle and saccule) of the balancing apparatus. The oval window on its lateral wall is occupied by the base of the STAPES of the MIDDLE EAR.
Antibiotic complex produced by Streptomyces fradiae. It is composed of neomycins A, B, and C. It acts by inhibiting translation during protein synthesis.
The electric response of the cochlear hair cells to acoustic stimulation.
Clusters of neuronal cell bodies in invertebrates. Invertebrate ganglia may also contain neuronal processes and non-neuronal supporting cells. Many invertebrate ganglia are favorable subjects for research because they have small numbers of functional neuronal types which can be identified from one animal to another.
The domestic cat, Felis catus, of the carnivore family FELIDAE, comprising over 30 different breeds. The domestic cat is descended primarily from the wild cat of Africa and extreme southwestern Asia. Though probably present in towns in Palestine as long ago as 7000 years, actual domestication occurred in Egypt about 4000 years ago. (From Walker's Mammals of the World, 6th ed, p801)
Histochemical localization of immunoreactive substances using labeled antibodies as reagents.
A subfamily of the Muridae consisting of several genera including Gerbillus, Rhombomys, Tatera, Meriones, and Psammomys.
Use of electric potential or currents to elicit biological responses.
The largest and uppermost of the paravertebral sympathetic ganglia.
Specialized afferent neurons capable of transducing sensory stimuli into NERVE IMPULSES to be transmitted to the CENTRAL NERVOUS SYSTEM. Sometimes sensory receptors for external stimuli are called exteroceptors; for internal stimuli are called interoceptors and proprioceptors.
Neuroglial cells of the peripheral nervous system which form the insulating myelin sheaths of peripheral axons.
'Nerve tissue proteins' are specialized proteins found within the nervous system's biological tissue, including neurofilaments, neuronal cytoskeletal proteins, and neural cell adhesion molecules, which facilitate structural support, intracellular communication, and synaptic connectivity essential for proper neurological function.
Renewal or physiological repair of damaged nerve tissue.
The electrical properties, characteristics of living organisms, and the processes of organisms or their parts that are involved in generating and responding to electrical charges.
Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.
The number of CELLS of a specific kind, usually measured per unit volume or area of sample.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Measurement of hearing based on the use of pure tones of various frequencies and intensities as auditory stimuli.
Naturally occurring or experimentally induced animal diseases with pathological processes sufficiently similar to those of human diseases. They are used as study models for human diseases.
The posterior pair of the quadrigeminal bodies which contain centers for auditory function.
A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions.
Self-generated faint acoustic signals from the inner ear (COCHLEA) without external stimulation. These faint signals can be recorded in the EAR CANAL and are indications of active OUTER AUDITORY HAIR CELLS. Spontaneous otoacoustic emissions are found in all classes of land vertebrates.
The bony plate which extends outwards from the modiolus into the spiral canal of the cochlea, forming part of the structure that divides the upper SCALA VESTIBULI and the lower SCALA TYMPANI.
Formation of NEURONS which involves the differentiation and division of STEM CELLS in which one or both of the daughter cells become neurons.

AMPA-preferring glutamate receptors in cochlear physiology of adult guinea-pig. (1/269)

1. The present study was designed to determine which glutamate (Glu) receptors are involved in excitatory neurotransmission at the first auditory synapse between the inner hair cells and the spiral ganglion neurons. 2. The Glu receptors present at the membrane level were investigated on isolated spiral ganglion neuron somata from guinea-pigs by whole-cell voltage-clamp measurements. Glu and AMPA induced a fast onset inward current that was rapidly desensitized, while kainate induced only a non-desensitizing, steady-state current. NMDA induced no detectable current. 3. To further discriminate between the AMPA and kainate receptors present, we used the receptor-specific desensitization blockers, cyclothiazide and concanavalin A. While no effect was observed with concanavalin A, cyclothiazide greatly enhanced the Glu-, AMPA- and kainate-induced steady-state currents and potentiated Glu-induced membrane depolarization. 4. To extrapolate the results obtained from the somata to the events occurring in situ at the dendrites, the effects of these drugs were evaluated in vivo. Cyclothiazide reversibly increased spontaneous activity of single auditory nerve fibres, while concanavalin A had no effect, suggesting that the functional Glu receptors on the somata may be the same as those at the dendrites. 5. The combination of a moderate-level sound together with cyclothiazide increased and subsequently abolished the spontaneous and the sound-evoked activity of the auditory nerve fibres. Histological examination revealed destruction of the dendrites, suggesting that cyclothiazide potentiates sound-induced Glu excitotoxicity via AMPA receptors. 6. Our results reveal that fast synaptic transmission in the cochlea is mainly mediated by desensitizing AMPA receptors.  (+info)

Expression of an inwardly rectifying K(+) channel, Kir4.1, in satellite cells of rat cochlear ganglia. (2/269)

Satellite cells are glial cells wrapped around somata of sensory and autonomic ganglion neurons. Neither their functional roles nor electrical properties have been fully clarified so far. Using immunohistochemistry, we found that inwardly rectifying K(+) channel subunit Kir4.1 (also called Kir1.2 or K(AB)-2) was expressed prominently in the satellite cells of cochlear ganglia. The Kir4.1 immunoreactivity was localized specifically at the myelin sheaths of satellite cells wrapping the somata of the ganglion neurons. Developmental expression of Kir4.1 in satellite cells paralleled development of the action potential in the auditory nerve. These results suggest that this channel in satellite cells may be responsible for the regulation of K(+) extruded from the ganglion neurons during excitation.  (+info)

Electrical cochlear stimulation in the deaf cat: comparisons between psychophysical and central auditory neuronal thresholds. (3/269)

Cochlear prostheses for electrical stimulation of the auditory nerve ("electrical hearing") can provide auditory capacity for profoundly deaf adults and children, including in many cases a restored ability to perceive speech without visual cues. A fundamental challenge in auditory neuroscience is to understand the neural and perceptual mechanisms that make rehabilitation of hearing possible in these deaf humans. We have developed a feline behavioral model that allows us to study behavioral and physiological variables in the same deaf animals. Cats deafened by injection of ototoxic antibiotics were implanted with either a monopolar round window electrode or a multichannel scala tympani electrode array. To evaluate the effects of perceptually significant electrical stimulation of the auditory nerve on the central auditory system, an animal was trained to avoid a mild electrocutaneous shock when biphasic current pulses (0.2 ms/phase) were delivered to its implanted cochlea. Psychophysical detection thresholds and electrical auditory brain stem response (EABR) thresholds were estimated in each cat. At the conclusion of behavioral testing, acute physiological experiments were conducted, and threshold responses were recorded for single neurons and multineuronal clusters in the central nucleus of the inferior colliculus (ICC) and the primary auditory cortex (A1). Behavioral and neurophysiological thresholds were evaluated with reference to cochlear histopathology in the same deaf cats. The results of the present study include: 1) in the cats implanted with a scala tympani electrode array, the lowest ICC and A1 neural thresholds were virtually identical to the behavioral thresholds for intracochlear bipolar stimulation; 2) behavioral thresholds were lower than ICC and A1 neural thresholds in each of the cats implanted with a monopolar round window electrode; 3) EABR thresholds were higher than behavioral thresholds in all of the cats (mean difference = 6.5 dB); and 4) the cumulative number of action potentials for a sample of ICC neurons increased monotonically as a function of the amplitude and the number of stimulating biphasic pulses. This physiological result suggests that the output from the ICC may be integrated spatially across neurons and temporally integrated across pulses when the auditory nerve array is stimulated with a train of biphasic current pulses. Because behavioral thresholds were lower and reaction times were faster at a pulse rate of 30 pps compared with a pulse rate of 2 pps, spatial-temporal integration in the central auditory system was presumably reflected in psychophysical performance.  (+info)

Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems. (4/269)

BETA2/NeuroD1 is a bHLH transcription factor that is expressed during development in the mammalian pancreas and in many locations in the central and peripheral nervous systems. During inner ear ontogenesis, it is present in both sensory ganglion neurons and sensory epithelia. Although studies have shown that BETA2/NeuroD1 is important in the development of the hippocampal dentate gyrus and the cerebellum, its functions in the peripheral nervous system and in particular in the inner ear are unclear. Mice carrying a BETA2/NeuroD1 null mutation exhibit behavioral abnormalities suggestive of an inner ear defect, including lack of responsiveness to sound, hyperactivity, head tilting, and circling. Here we show that these defects can be explained by a severe reduction of sensory neurons in the cochlear-vestibular ganglion (CVG). A developmental study of CVG formation in the null demonstrates that BETA2/NeuroD1 does not play a primary role in the proliferation of neuroblast precursors or in their decision to become neuroblasts. Instead, the reduction in CVG neuron number is caused by a combination both of delayed or defective delamination of CVG neuroblast precursors from the otic vesicle epithelium and of enhanced apoptosis both in the otic epithelium and among those neurons that do delaminate to form the CVG. There are also defects in differentiation and patterning of the cochlear duct and sensory epithelium and loss of the dorsal cochlear nucleus. BETA2/NeuroD1 is, thus, the first gene to be shown to regulate neuronal and sensory cell development in both the cochlear and vestibular systems.  (+info)

Multiple distinct signal pathways, including an autocrine neurotrophic mechanism, contribute to the survival-promoting effect of depolarization on spiral ganglion neurons in vitro. (5/269)

We have shown previously that BDNF, neurotrophin-3 (NT-3), chlorphenylthio-cAMP (cpt-cAMP) (a permeant cAMP analog), and membrane depolarization promote spiral ganglion neuron (SGN) survival in vitro in an additive manner, depolarization having the greatest efficacy. Expression of both BDNF and of NT-3 is detectable in cultured SGNs after plating in either depolarizing or nondepolarizing medium. These neurotrophins promote survival by an autocrine mechanism; TrkB-IgG or TrkC-IgG, which block neurotrophin binding to, respectively, TrkB and TrkC, partially inhibit the trophic effect of depolarization. The mitogen-activated protein kinase kinase inhibitor PD98059 and the phosphatidylinositol-3-OH kinase inhibitor LY294002 both abolish trophic support by neurotrophins but only partially inhibit support by depolarization. Inhibition by these compounds is not additive with inhibition by Trk-IgGs. The cAMP antagonist Rp-adenosine-3',5'-cyclic-phosphorothioate (Rp-cAMPS) abolishes survival attributable to cpt-cAMP but has no effect on that attributable to neurotrophins, nor do inhibitors of neurotrophin-dependent survival affect survival attributable to cpt-cAMP. However, Rp-cAMPS does partially inhibit depolarization-dependent survival, an inhibition that is additive with that by Trk-IgGs, PD98059, or LY294002. Moreover, Rp-cAMPS prevents depolarization-dependent survival of PC12 cells maintained in subthreshold levels of NGF. Inhibition of Ca(2+)/calmodulin-dependent protein kinases (CaMKs) with KN-62 reduces SGN survival independently of Rp-cAMPS, Trk-IgGs, and LY294002 and additively with them. Combined inhibition of Trk, cAMP, and CaMK signaling prevents depolarization-dependent survival. Thus, survival of SGNs under depolarizing conditions involves additivity among a depolarization-independent autocrine pathway, a cAMP-dependent pathway, and a CaMK-dependent pathway.  (+info)

HSV amplicon-mediated neurotrophin-3 expression protects murine spiral ganglion neurons from cisplatin-induced damage. (6/269)

Ototoxicity is a major dose-limiting side effect of cisplatin (DDP) administration due to its propensity to induce destruction of hair cells and neurons in the auditory system. Previous studies demonstrated that TrkC-expressing spiral ganglion neurons (SGN) are protected from the cytotoxic effects of DDP by localized delivery of the trophic factor neurotrophin-3 (NT-3). Successful in vivo implementation of such a therapy requires the development of an efficient gene delivery vehicle for expression of NT-3 within the cochlea. To this end, we constructed a herpes simplex virus (HSV) amplicon vector that expressed a c-Myc-tagged NT-3 chimera (HSVnt-3myc). Helper virus-free vector stocks were initially evaluated in vitro for their capacity to direct expression of NT-3 mRNA and protein. Transduction of cultured murine cochlear explants with HSVnt-3myc resulted in production of NT-3 mRNA and protein up to 3 ng/ml as measured over a 48-h period in culture supernatants. To determine whether NT-3 overexpression could abrogate DDP toxicity, cochlear explants were transduced with HSVnt-3myc or a murine intestinal alkaline phosphatase-expressing control vector, HSVmiap, and then exposed to cisplatin. HSVnt-3myc-transduced cochlear explants harbored significantly greater numbers of surviving SGNs than those infected with control virus. These data demonstrate that amplicon-mediated NT-3 transduction can attenuate the ototoxic action of DDP on organotypic culture. The potency of NT-3 in protecting spiral ganglion neurons from degeneration suggests that in vivo neurotrophin-based gene therapy may be useful for the prevention and/or treatment of hearing disorders.  (+info)

Spatial shaping of cochlear innervation by temporally regulated neurotrophin expression. (7/269)

Previous work suggested qualitatively different effects of neurotrophin 3 (NT-3) in cochlear innervation patterning in different null mutants. We now show that all NT-3 null mutants have a similar phenotype and lose all neurons in the basal turn of the cochlea. To understand these longitudinal deficits in neurotrophin mutants, we have compared the development of the deficit in the NT-3 mutant to the spatial-temporal expression patterns of brain-derived neurotrophic factor (BDNF) and NT-3, using lacZ reporters in each gene and with expression of the specific neurotrophin receptors, trkB and trkC. In the NT-3 mutant, almost normal numbers of spiral ganglion neurons form, but fiber outgrowth to the basal turn is eliminated by embryonic day (E) 13.5. Most neurons are lost between E13.5 and E15.5. During the period preceding apoptosis, NT-3 is expressed in supporting cells, whereas BDNF is expressed mainly in hair cells, which become postmitotic in an apical to basal temporal gradient. During the period of neuronal loss, BDNF is absent from the basal cochlea, accounting for the complete loss of basal turn neurons in the NT-3 mutant. The spatial gradients of neuronal loss in these two mutants appear attributable to spatial-temporal gradients of neurotrophin expression. Our immunocytochemical data show equal expression of their receptors, TrkB and TrkC, in spiral sensory neurons and thus do not relate to the basal turn loss. Mice in which NT-3 was replaced by BDNF show a qualitative normal pattern of innervation at E13.5. This suggests that the pattern of expression of neurotrophins rather than their receptors is essential for the spatial loss of spiral sensory neurons in NT-3 null mutants.  (+info)

Brn3a is a transcriptional regulator of soma size, target field innervation and axon pathfinding of inner ear sensory neurons. (8/269)

The POU domain transcription factors Brn3a, Brn3b and Brn3c are required for the proper development of sensory ganglia, retinal ganglion cells, and inner ear hair cells, respectively. We have investigated the roles of Brn3a in neuronal differentiation and target innervation in the facial-stato-acoustic ganglion. We show that absence of Brn3a results in a substantial reduction in neuronal size, abnormal neuronal migration and downregulation of gene expression, including that of the neurotrophin receptor TrkC, parvalbumin and Brn3b. Selective loss of TrkC neurons in the spiral ganglion of Brn3a(-/-) cochlea leads to an innervation defect similar to that of TrkC(-/-) mice. Most remarkably, our results uncover a novel role for Brn3a in regulating axon pathfinding and target field innervation by spiral and vestibular ganglion neurons. Loss of Brn3a results in severe retardation in development of the axon projections to the cochlea and the posterior vertical canal as early as E13.5. In addition, efferent axons that use the afferent fibers as a scaffold during pathfinding also show severe misrouting. Interestingly, despite the well-established roles of ephrins and EphB receptors in axon pathfinding, expression of these molecules does not appear to be affected in Brn3a(-/-) mice. Thus, Brn3a must control additional downstream genes that are required for axon pathfinding.  (+info)

The spiral ganglion is a structure located in the inner ear, specifically within the cochlea. It consists of nerve cell bodies that form the sensory component of the auditory nervous system. The spiral ganglion's neurons are bipolar and have peripheral processes that form synapses with hair cells in the organ of Corti, which is responsible for converting sound vibrations into electrical signals.

The central processes of these neurons then coalesce to form the cochlear nerve, which transmits these electrical signals to the brainstem and ultimately to the auditory cortex for processing and interpretation as sound. Damage to the spiral ganglion or its associated neural structures can lead to hearing loss or deafness.

The cochlea is a part of the inner ear that is responsible for hearing. It is a spiral-shaped structure that looks like a snail shell and is filled with fluid. The cochlea contains hair cells, which are specialized sensory cells that convert sound vibrations into electrical signals that are sent to the brain.

The cochlea has three main parts: the vestibular canal, the tympanic canal, and the cochlear duct. Sound waves enter the inner ear and cause the fluid in the cochlea to move, which in turn causes the hair cells to bend. This bending motion stimulates the hair cells to generate electrical signals that are sent to the brain via the auditory nerve.

The brain then interprets these signals as sound, allowing us to hear and understand speech, music, and other sounds in our environment. Damage to the hair cells or other structures in the cochlea can lead to hearing loss or deafness.

The cochlear nerve, also known as the auditory nerve, is the sensory nerve that transmits sound signals from the inner ear to the brain. It consists of two parts: the outer spiral ganglion and the inner vestibular portion. The spiral ganglion contains the cell bodies of the bipolar neurons that receive input from hair cells in the cochlea, which is the snail-shaped organ in the inner ear responsible for hearing. These neurons then send their axons to form the cochlear nerve, which travels through the internal auditory meatus and synapses with neurons in the cochlear nuclei located in the brainstem.

Damage to the cochlear nerve can result in hearing loss or deafness, depending on the severity of the injury. Common causes of cochlear nerve damage include acoustic trauma, such as exposure to loud noises, viral infections, meningitis, and tumors affecting the nerve or surrounding structures. In some cases, cochlear nerve damage may be treated with hearing aids, cochlear implants, or other assistive devices to help restore or improve hearing function.

Deafness is a hearing loss that is so severe that it results in significant difficulty in understanding or comprehending speech, even when using hearing aids. It can be congenital (present at birth) or acquired later in life due to various causes such as disease, injury, infection, exposure to loud noises, or aging. Deafness can range from mild to profound and may affect one ear (unilateral) or both ears (bilateral). In some cases, deafness may be accompanied by tinnitus, which is the perception of ringing or other sounds in the ears.

Deaf individuals often use American Sign Language (ASL) or other forms of sign language to communicate. Some people with less severe hearing loss may benefit from hearing aids, cochlear implants, or other assistive listening devices. Deafness can have significant social, educational, and vocational implications, and early intervention and appropriate support services are critical for optimal development and outcomes.

The Organ of Corti is the sensory organ of hearing within the cochlea of the inner ear. It is a structure in the inner spiral sulcus of the cochlear duct and is responsible for converting sound vibrations into electrical signals that are sent to the brain via the auditory nerve.

The Organ of Corti consists of hair cells, which are sensory receptors with hair-like projections called stereocilia on their apical surfaces. These stereocilia are embedded in a gelatinous matrix and are arranged in rows of different heights. When sound vibrations cause the fluid in the cochlea to move, the stereocilia bend, which opens ion channels and triggers nerve impulses that are sent to the brain.

Damage or loss of hair cells in the Organ of Corti can result in hearing loss, making it a critical structure for maintaining normal auditory function.

Spiral Computed Tomography (CT), also known as Helical CT, is a type of computed tomography scan in which the X-ray tube and detector rotate around the patient in a spiral path, capturing data as the table moves the patient through the scanner. This continuous spiral motion allows for faster and more detailed volumetric imaging of internal organs and structures, reducing the need for multiple slices and providing improved image reconstruction. It is commonly used to diagnose and monitor various medical conditions, including cancer, heart disease, and trauma injuries.

Auditory brainstem evoked potentials (ABEPs or BAEPs) are medical tests that measure the electrical activity in the auditory pathway of the brain in response to sound stimulation. The test involves placing electrodes on the scalp and recording the tiny electrical signals generated by the nerve cells in the brainstem as they respond to clicks or tone bursts presented through earphones.

The resulting waveform is analyzed for latency (the time it takes for the signal to travel from the ear to the brain) and amplitude (the strength of the signal). Abnormalities in the waveform can indicate damage to the auditory nerve or brainstem, and are often used in the diagnosis of various neurological conditions such as multiple sclerosis, acoustic neuroma, and brainstem tumors.

The test is non-invasive, painless, and takes only a few minutes to perform. It provides valuable information about the functioning of the auditory pathway and can help guide treatment decisions for patients with hearing or balance disorders.

A ganglion is a cluster of neuron cell bodies in the peripheral nervous system. Ganglia are typically associated with nerves and serve as sites for sensory processing, integration, and relay of information between the periphery and the central nervous system (CNS). The two main types of ganglia are sensory ganglia, which contain pseudounipolar neurons that transmit sensory information to the CNS, and autonomic ganglia, which contain multipolar neurons that control involuntary physiological functions.

Examples of sensory ganglia include dorsal root ganglia (DRG), which are associated with spinal nerves, and cranial nerve ganglia, such as the trigeminal ganglion. Autonomic ganglia can be further divided into sympathetic and parasympathetic ganglia, which regulate different aspects of the autonomic nervous system.

It's worth noting that in anatomy, "ganglion" refers to a group of nerve cell bodies, while in clinical contexts, "ganglion" is often used to describe a specific type of cystic structure that forms near joints or tendons, typically in the wrist or foot. These ganglia are not related to the peripheral nervous system's ganglia but rather are fluid-filled sacs that may cause discomfort or pain due to their size or location.

Auditory hair cells are specialized sensory receptor cells located in the inner ear, more specifically in the organ of Corti within the cochlea. They play a crucial role in hearing by converting sound vibrations into electrical signals that can be interpreted by the brain.

These hair cells have hair-like projections called stereocilia on their apical surface, which are embedded in a gelatinous matrix. When sound waves reach the inner ear, they cause the fluid within the cochlea to move, which in turn causes the stereocilia to bend. This bending motion opens ion channels at the tips of the stereocilia, allowing positively charged ions (such as potassium) to flow into the hair cells and trigger a receptor potential.

The receptor potential then leads to the release of neurotransmitters at the base of the hair cells, which activate afferent nerve fibers that synapse with these cells. The electrical signals generated by this process are transmitted to the brain via the auditory nerve, where they are interpreted as sound.

There are two types of auditory hair cells: inner hair cells and outer hair cells. Inner hair cells are the primary sensory receptors responsible for transmitting information about sound to the brain. They make direct contact with afferent nerve fibers and are more sensitive to mechanical stimulation than outer hair cells.

Outer hair cells, on the other hand, are involved in amplifying and fine-tuning the mechanical response of the inner ear to sound. They have a unique ability to contract and relax in response to electrical signals, which allows them to adjust the stiffness of their stereocilia and enhance the sensitivity of the cochlea to different frequencies.

Damage or loss of auditory hair cells can lead to hearing impairment or deafness, as these cells cannot regenerate spontaneously in mammals. Therefore, understanding the structure and function of hair cells is essential for developing therapies aimed at treating hearing disorders.

Labyrinth supporting cells are specialized cells that are located in the inner ear and provide structural and functional support to the sensory hair cells within the labyrinth, which is the complex system of tubes and sacs responsible for maintaining balance and hearing. These supporting cells form a crucial part of the architecture of the inner ear and help to maintain the proper functioning of the sensory hair cells by providing mechanical support, contributing to the development and maintenance of the extracellular matrix, and playing a role in the recycling of neurotransmitters. Additionally, labyrinth supporting cells can also transform into new hair cells in certain circumstances, which has implications for potential regenerative therapies aimed at treating hearing loss and balance disorders.

Presbycusis is an age-related hearing loss, typically characterized by the progressive loss of sensitivity to high-frequency sounds. It's a result of natural aging of the auditory system and is often seen as a type of sensorineural hearing loss. The term comes from the Greek words "presbus" meaning old man and "akousis" meaning hearing.

This condition usually develops slowly over many years and can affect both ears equally. Presbycusis can make understanding speech, especially in noisy environments, quite challenging. It's a common condition, and its prevalence increases with age. While it's not reversible, various assistive devices like hearing aids can help manage the symptoms.

Retinal Ganglion Cells (RGCs) are a type of neuron located in the innermost layer of the retina, the light-sensitive tissue at the back of the eye. These cells receive visual information from photoreceptors (rods and cones) via intermediate cells called bipolar cells. RGCs then send this visual information through their long axons to form the optic nerve, which transmits the signals to the brain for processing and interpretation as vision.

There are several types of RGCs, each with distinct morphological and functional characteristics. Some RGCs are specialized in detecting specific features of the visual scene, such as motion, contrast, color, or brightness. The diversity of RGCs allows for a rich and complex representation of the visual world in the brain.

Damage to RGCs can lead to various visual impairments, including loss of vision, reduced visual acuity, and altered visual fields. Conditions associated with RGC damage or degeneration include glaucoma, optic neuritis, ischemic optic neuropathy, and some inherited retinal diseases.

Neurotrophin 3 (NT-3) is a protein that belongs to the family of neurotrophic factors, which are essential for the growth, survival, and differentiation of neurons. NT-3 specifically plays a crucial role in the development and maintenance of the nervous system, particularly in the peripheral nervous system. It has high affinity binding to two receptors: TrkC and p75NTR. The activation of these receptors by NT-3 promotes the survival and differentiation of sensory neurons, motor neurons, and some sympathetic neurons. Additionally, it contributes to the regulation of synaptic plasticity and neural circuit formation during development and in adulthood.

Spinal ganglia, also known as dorsal root ganglia, are clusters of nerve cell bodies located in the peripheral nervous system. They are situated along the length of the spinal cord and are responsible for transmitting sensory information from the body to the brain. Each spinal ganglion contains numerous neurons, or nerve cells, with long processes called axons that extend into the periphery and innervate various tissues and organs. The cell bodies within the spinal ganglia receive sensory input from these axons and transmit this information to the central nervous system via the dorsal roots of the spinal nerves. This allows the brain to interpret and respond to a wide range of sensory stimuli, including touch, temperature, pain, and proprioception (the sense of the position and movement of one's body).

Auditory inner hair cells are specialized sensory receptor cells located in the inner ear, more specifically in the organ of Corti within the cochlea. They play a crucial role in hearing by converting mechanical sound energy into electrical signals that can be processed and interpreted by the brain.

Human ears have about 3,500 inner hair cells arranged in one row along the length of the basilar membrane in each cochlea. These hair cells are characterized by their stereocilia, which are hair-like projections on the apical surface that are embedded in a gelatinous matrix called the tectorial membrane.

When sound waves cause the basilar membrane to vibrate, the stereocilia of inner hair cells bend and deflect. This deflection triggers a cascade of biochemical events leading to the release of neurotransmitters at the base of the hair cell. These neurotransmitters then stimulate the afferent auditory nerve fibers (type I fibers) that synapse with the inner hair cells, transmitting the electrical signals to the brain for further processing and interpretation as sound.

Damage or loss of these inner hair cells can lead to significant hearing impairment or deafness, as they are essential for normal auditory function. Currently, there is no effective way to regenerate damaged inner hair cells in humans, making hearing loss due to their damage permanent.

The basal ganglia are a group of interconnected nuclei, or clusters of neurons, located in the base of the brain. They play a crucial role in regulating motor function, cognition, and emotion. The main components of the basal ganglia include the striatum (made up of the caudate nucleus, putamen, and ventral striatum), globus pallidus (divided into external and internal segments), subthalamic nucleus, and substantia nigra (with its pars compacta and pars reticulata).

The basal ganglia receive input from various regions of the cerebral cortex and other brain areas. They process this information and send output back to the thalamus and cortex, helping to modulate and coordinate movement. The basal ganglia also contribute to higher cognitive functions such as learning, decision-making, and habit formation. Dysfunction in the basal ganglia can lead to neurological disorders like Parkinson's disease, Huntington's disease, and dystonia.

Sympathetic ganglia are part of the autonomic nervous system, which controls involuntary bodily functions. These ganglia are clusters of nerve cell bodies located outside the central nervous system, along the spinal cord. They serve as a relay station for signals sent from the central nervous system to the organs and glands. The sympathetic ganglia are responsible for the "fight or flight" response, releasing neurotransmitters such as norepinephrine that prepare the body for action in response to stress or danger.

Stria vascularis is a highly vascularized (rich in blood vessels) structure located in the cochlea of the inner ear. It plays a crucial role in the process of hearing by maintaining the endocochlear potential, which is essential for the conversion of sound waves into electrical signals that can be interpreted by the brain. The stria vascularis is composed of three layers: the marginal cells, intermediate cells, and basal cells, which work together to maintain the ionic balance and generate the endocochlear potential. Damage to the stria vascularis can result in hearing loss.

The round window ( membrana tympani rotunda) is a small, thin membrane-covered opening located in the inner ear between the middle ear and the cochlea. It serves as one of the two openings that lead into the cochlea, with the other being the oval window.

The round window's primary function is to help regulate and dampen the pressure changes within the cochlea that occur when sound waves reach the inner ear. This is accomplished through the movement of the fluid-filled spaces inside the cochlea (the scala vestibuli and scala tympani) caused by vibrations from the stapes bone, which connects to the oval window.

As the stapes bone moves in response to sound waves, it causes a corresponding motion in the perilymph fluid within the cochlea. This movement then creates pressure changes at the round window, causing it to bulge outward or move inward. The flexibility of the round window allows it to absorb and dissipate these pressure changes, which helps protect the delicate structures inside the inner ear from damage due to excessive pressure buildup.

It is important to note that any damage or dysfunction in the round window can negatively impact hearing ability and cause various hearing disorders.

Autonomic ganglia are collections of neurons located outside the central nervous system (CNS) that are a part of the autonomic nervous system (ANS). The ANS is responsible for controlling various involuntary physiological functions such as heart rate, digestion, respiratory rate, pupillary response, urination, and sexual arousal.

Autonomic ganglia receive inputs from preganglionic neurons, whose cell bodies are located in the CNS, and send outputs to effector organs through postganglionic neurons. The autonomic ganglia can be divided into two main subsystems: the sympathetic and parasympathetic systems.

Sympathetic ganglia are typically located close to the spinal cord and receive inputs from preganglionic neurons whose cell bodies are located in the thoracic and lumbar regions of the spinal cord. The postganglionic neurons of the sympathetic system release noradrenaline (also known as norepinephrine) as their primary neurotransmitter, which acts on effector organs to produce a range of responses such as increasing heart rate and blood pressure, dilating pupils, and promoting glucose mobilization.

Parasympathetic ganglia are typically located closer to the target organs and receive inputs from preganglionic neurons whose cell bodies are located in the brainstem and sacral regions of the spinal cord. The postganglionic neurons of the parasympathetic system release acetylcholine as their primary neurotransmitter, which acts on effector organs to produce a range of responses such as decreasing heart rate and blood pressure, constricting pupils, and promoting digestion and urination.

Overall, autonomic ganglia play a critical role in regulating various physiological functions that are essential for maintaining homeostasis in the body.

Cochlear implants are medical devices that are surgically implanted in the inner ear to help restore hearing in individuals with severe to profound hearing loss. These devices bypass the damaged hair cells in the inner ear and directly stimulate the auditory nerve, allowing the brain to interpret sound signals. Cochlear implants consist of two main components: an external processor that picks up and analyzes sounds from the environment, and an internal receiver/stimulator that receives the processed information and sends electrical impulses to the auditory nerve. The resulting patterns of electrical activity are then perceived as sound by the brain. Cochlear implants can significantly improve communication abilities, language development, and overall quality of life for individuals with profound hearing loss.

The cochlear duct, also known as the scala media, is a membranous duct located within the cochlea of the inner ear. It is one of three fluid-filled compartments in the cochlea, along with the vestibular duct (scala vestibuli) and the tympanic duct (scala tympani).

The cochlear duct contains endolymph, a specialized fluid that carries electrical signals to the auditory nerve. The organ of Corti, which is responsible for converting sound vibrations into electrical signals, is located within the cochlear duct.

The cochlear duct runs along the length of the cochlea and is separated from the vestibular duct by Reissner's membrane and from the tympanic duct by the basilar membrane. These membranes help to create a highly sensitive and selective environment for sound perception, allowing us to hear and distinguish different frequencies and intensities of sound.

Hearing is the ability to perceive sounds by detecting vibrations in the air or other mediums and translating them into nerve impulses that are sent to the brain for interpretation. In medical terms, hearing is defined as the sense of sound perception, which is mediated by the ear and interpreted by the brain. It involves a complex series of processes, including the conduction of sound waves through the outer ear to the eardrum, the vibration of the middle ear bones, and the movement of fluid in the inner ear, which stimulates hair cells to send electrical signals to the auditory nerve and ultimately to the brain. Hearing allows us to communicate with others, appreciate music and sounds, and detect danger or important events in our environment.

Neurons, also known as nerve cells or neurocytes, are specialized cells that constitute the basic unit of the nervous system. They are responsible for receiving, processing, and transmitting information and signals within the body. Neurons have three main parts: the dendrites, the cell body (soma), and the axon. The dendrites receive signals from other neurons or sensory receptors, while the axon transmits these signals to other neurons, muscles, or glands. The junction between two neurons is called a synapse, where neurotransmitters are released to transmit the signal across the gap (synaptic cleft) to the next neuron. Neurons vary in size, shape, and structure depending on their function and location within the nervous system.

Hearing loss is a partial or total inability to hear sounds in one or both ears. It can occur due to damage to the structures of the ear, including the outer ear, middle ear, inner ear, or nerve pathways that transmit sound to the brain. The degree of hearing loss can vary from mild (difficulty hearing soft sounds) to severe (inability to hear even loud sounds). Hearing loss can be temporary or permanent and may be caused by factors such as exposure to loud noises, genetics, aging, infections, trauma, or certain medical conditions. It is important to note that hearing loss can have significant impacts on a person's communication abilities, social interactions, and overall quality of life.

The trigeminal ganglion, also known as the semilunar or Gasserian ganglion, is a sensory ganglion (a cluster of nerve cell bodies) located near the base of the skull. It is a part of the trigeminal nerve (the fifth cranial nerve), which is responsible for sensation in the face and motor functions such as biting and chewing.

The trigeminal ganglion contains the cell bodies of sensory neurons that carry information from three major branches of the trigeminal nerve: the ophthalmic, maxillary, and mandibular divisions. These divisions provide sensation to different areas of the face, head, and oral cavity, including the skin, mucous membranes, muscles, and teeth.

Damage to the trigeminal ganglion or its nerve branches can result in various sensory disturbances, such as pain, numbness, or tingling in the affected areas. Conditions like trigeminal neuralgia, a disorder characterized by intense, stabbing facial pain, may involve the trigeminal ganglion and its associated nerves.

Brain-Derived Neurotrophic Factor (BDNF) is a type of protein called a neurotrophin, which is involved in the growth and maintenance of neurons (nerve cells) in the brain. BDNFA is encoded by the BDNF gene and is widely expressed throughout the central nervous system. It plays an essential role in supporting the survival of existing neurons, encouraging the growth and differentiation of new neurons and synapses, and contributing to neuroplasticity - the ability of the brain to change and adapt as a result of experience. Low levels of BDNF have been associated with several neurological disorders, including depression, Alzheimer's disease, and Huntington's disease.

The inner ear is the innermost part of the ear that contains the sensory organs for hearing and balance. It consists of a complex system of fluid-filled tubes and sacs called the vestibular system, which is responsible for maintaining balance and spatial orientation, and the cochlea, a spiral-shaped organ that converts sound vibrations into electrical signals that are sent to the brain.

The inner ear is located deep within the temporal bone of the skull and is protected by a bony labyrinth. The vestibular system includes the semicircular canals, which detect rotational movements of the head, and the otolith organs (the saccule and utricle), which detect linear acceleration and gravity.

Damage to the inner ear can result in hearing loss, tinnitus (ringing in the ears), vertigo (a spinning sensation), and balance problems.

Sensorineural hearing loss (SNHL) is a type of hearing impairment that occurs due to damage to the inner ear (cochlea) or to the nerve pathways from the inner ear to the brain. It can be caused by various factors such as aging, exposure to loud noises, genetics, certain medical conditions (like diabetes and heart disease), and ototoxic medications.

SNHL affects the ability of the hair cells in the cochlea to convert sound waves into electrical signals that are sent to the brain via the auditory nerve. As a result, sounds may be perceived as muffled, faint, or distorted, making it difficult to understand speech, especially in noisy environments.

SNHL is typically permanent and cannot be corrected with medication or surgery, but hearing aids or cochlear implants can help improve communication and quality of life for those affected.

Cochlear diseases refer to conditions that affect the structure or function of the cochlea, which is a part of the inner ear responsible for hearing. These diseases can cause various types and degrees of hearing loss, ranging from mild to profound. Some common cochlear diseases include:

1. Cochlear otosclerosis: A condition where there is abnormal bone growth in the cochlea, which can lead to conductive or sensorineural hearing loss.
2. Cochlear Meniere's disease: A disorder that affects the inner ear and causes vertigo, tinnitus, and fluctuating hearing loss.
3. Cochlear damage due to exposure to loud noises: Prolonged or sudden exposure to loud noises can cause permanent cochlear damage and hearing loss.
4. Presbycusis: Age-related hearing loss that affects the cochlea and other structures of the auditory system.
5. Cochlear nerve tumors: Rare benign or malignant growths on the cochlear nerve can cause hearing loss, tinnitus, and balance problems.
6. Infections: Bacterial or viral infections such as meningitis, labyrinthitis, or otitis media can damage the cochlea and lead to hearing loss.
7. Ototoxicity: Certain medications can be toxic to the cochlea and cause hearing loss, tinnitus, or balance problems.
8. Genetic factors: Inherited genetic mutations can cause various types of cochlear diseases, such as connexin 26 deficiency, Waardenburg syndrome, or Usher syndrome.

It is important to note that early diagnosis and treatment of cochlear diseases can help prevent or minimize hearing loss and other complications.

The auditory threshold is the minimum sound intensity or loudness level that a person can detect 50% of the time, for a given tone frequency. It is typically measured in decibels (dB) and represents the quietest sound that a person can hear. The auditory threshold can be affected by various factors such as age, exposure to noise, and certain medical conditions. Hearing tests, such as pure-tone audiometry, are used to measure an individual's auditory thresholds for different frequencies.

Parasympathetic ganglia are collections of neurons located outside the central nervous system (CNS) that serve as relay stations for parasympathetic nerve impulses. The parasympathetic nervous system is one of the two subdivisions of the autonomic nervous system, which controls involuntary physiological responses.

The parasympathetic ganglia receive preganglionic fibers from the brainstem and sacral regions of the spinal cord. After synapsing in these ganglia, postganglionic fibers innervate target organs such as the heart, glands, and smooth muscles. The primary function of the parasympathetic nervous system is to promote rest, digestion, and energy conservation.

Parasympathetic ganglia are typically located close to or within the target organs they innervate. Examples include:

1. Ciliary ganglion: Innervates the ciliary muscle and iris sphincter in the eye, controlling accommodation and pupil constriction.
2. Pterygopalatine (sphenopalatine) ganglion: Supplies the lacrimal gland, mucous membranes of the nasal cavity, and palate, regulating tear production and nasal secretions.
3. Otic ganglion: Innervates the parotid gland, controlling salivary secretion.
4. Submandibular ganglion: Supplies the submandibular and sublingual salivary glands, regulating salivation.
5. Sacral parasympathetic ganglia: Located in the sacrum, they innervate the distal colon, rectum, and genitourinary organs, controlling defecation, urination, and sexual arousal.

These parasympathetic ganglia play crucial roles in maintaining homeostasis by regulating various bodily functions during rest and relaxation.

Cochlear implantation is a surgical procedure in which a device called a cochlear implant is inserted into the inner ear (cochlea) of a person with severe to profound hearing loss. The implant consists of an external component, which includes a microphone, processor, and transmitter, and an internal component, which includes a receiver and electrode array.

The microphone picks up sounds from the environment and sends them to the processor, which analyzes and converts the sounds into electrical signals. These signals are then transmitted to the receiver, which stimulates the electrode array in the cochlea. The electrodes directly stimulate the auditory nerve fibers, bypassing the damaged hair cells in the inner ear that are responsible for normal hearing.

The brain interprets these electrical signals as sound, allowing the person to perceive and understand speech and other sounds. Cochlear implantation is typically recommended for people who do not benefit from traditional hearing aids and can significantly improve communication, quality of life, and social integration for those with severe to profound hearing loss.

The spiral ligament of the cochlea is a fibrous structure located in the inner ear, more specifically in the cochlea. It is part of the membranous labyrinth and helps to maintain the shape and tension of the cochlear duct, which is essential for hearing.

The spiral ligament is attached to the bony wall of the cochlea and runs along the entire length of the cochlear duct, spiraling around it in a snail-like fashion. It consists of an outer, highly vascularized fibrous layer (the fibrous cap) and an inner, more cellular layer (the avascular zone).

The spiral ligament plays a crucial role in sound transmission and perception by helping to maintain the mechanical properties of the cochlear duct. The tension on the basilar membrane, where the sensory hair cells are located, is regulated by the spiral ligament's stiffness and elasticity. This tension affects the vibration amplitude and frequency selectivity of the basilar membrane, which in turn influences how we perceive different sounds and pitches.

Damage to the spiral ligament can result in hearing loss or impairment due to disrupted sound transmission and perception.

Sensory ganglia are clusters of nerve cell bodies located outside the central nervous system (the brain and spinal cord). They are primarily associated with sensory neurons, which are responsible for transmitting sensory information from various parts of the body to the central nervous system.

In humans, there are two main types of sensory ganglia: dorsal root ganglia and cranial nerve ganglia. Dorsal root ganglia are located along the spinal cord and contain the cell bodies of sensory neurons that innervate the skin, muscles, joints, and other tissues of the body. These neurons transmit information about touch, temperature, pain, and proprioception (the sense of the position and movement of the body).

Cranial nerve ganglia are associated with the cranial nerves, which are responsible for transmitting sensory information from the head and neck to the brain. For example, the trigeminal ganglion is a cranial nerve ganglion that contains the cell bodies of neurons that transmit sensory information from the face, mouth, and other structures of the head.

Overall, sensory ganglia play a critical role in our ability to perceive and interact with the world around us by transmitting important sensory information to the brain for processing.

Neurites are extensions of a neuron (a type of cell in the nervous system) that can be either an axon or a dendrite. An axon is a thin, cable-like extension that carries signals away from the cell body, while a dendrite is a branching extension that receives signals from other neurons. Neurites play a crucial role in the communication between neurons and the formation of neural networks. They are involved in the transmission of electrical and chemical signals, as well as in the growth and development of the nervous system.

Auditory outer hair cells are specialized sensory receptor cells located in the cochlea of the inner ear. They are part of the organ of Corti and play a crucial role in hearing by converting sound energy into electrical signals that can be interpreted by the brain.

Unlike the more numerous and simpler auditory inner hair cells, outer hair cells are equipped with unique actin-based molecular motors called "motile" or "piezoelectric" properties. These motors enable the outer hair cells to change their shape and length in response to electrical signals, which in turn amplifies the mechanical vibrations of the basilar membrane where they are located. This amplification increases the sensitivity and frequency selectivity of hearing, allowing us to detect and discriminate sounds over a wide range of intensities and frequencies.

Damage or loss of outer hair cells is a common cause of sensorineural hearing loss, which can result from exposure to loud noises, aging, genetics, ototoxic drugs, and other factors. Currently, there are no effective treatments to regenerate or replace damaged outer hair cells, making hearing loss an irreversible condition in most cases.

Nerve degeneration, also known as neurodegeneration, is the progressive loss of structure and function of neurons, which can lead to cognitive decline, motor impairment, and various other symptoms. This process occurs due to a variety of factors, including genetics, environmental influences, and aging. It is a key feature in several neurological disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, and multiple sclerosis. The degeneration can affect any part of the nervous system, leading to different symptoms depending on the location and extent of the damage.

Central hearing loss is a type of hearing disorder that occurs due to damage or dysfunction in the central auditory pathways of the brain, rather than in the ear itself. This condition can result from various causes, such as stroke, tumors, trauma, infection, or degenerative diseases affecting the brain.

In central hearing loss, the person may have difficulty understanding and processing speech, even when they can hear sounds at normal levels. They might experience problems with sound localization, discriminating between similar sounds, and comprehending complex auditory signals. This type of hearing loss is different from sensorineural or conductive hearing loss, which are related to issues in the outer, middle, or inner ear.

"Newborn animals" refers to the very young offspring of animals that have recently been born. In medical terminology, newborns are often referred to as "neonates," and they are classified as such from birth until about 28 days of age. During this time period, newborn animals are particularly vulnerable and require close monitoring and care to ensure their survival and healthy development.

The specific needs of newborn animals can vary widely depending on the species, but generally, they require warmth, nutrition, hydration, and protection from harm. In many cases, newborns are unable to regulate their own body temperature or feed themselves, so they rely heavily on their mothers for care and support.

In medical settings, newborn animals may be examined and treated by veterinarians to ensure that they are healthy and receiving the care they need. This can include providing medical interventions such as feeding tubes, antibiotics, or other treatments as needed to address any health issues that arise. Overall, the care and support of newborn animals is an important aspect of animal medicine and conservation efforts.

The Scala Tympani is a part of the inner ear's bony labyrinth, specifically within the cochlea. It is one of the two channels (the other being the Scala Vestibuli) that make up the bony duct of the cochlea, through which sound waves are transmitted to the inner ear.

The Scala Tympani starts at the round window, which is a membrane-covered opening located on the cochlea's outer wall. It runs parallel to the Scala Vestibuli and connects with it at the helicotrema, a small opening at the apex or tip of the cochlea.

When sound waves reach the inner ear, they cause vibrations in the fluid-filled Scala Tympani and Scala Vestibuli, which stimulate hair cells within the organ of Corti, leading to the conversion of mechanical energy into electrical signals that are then transmitted to the brain via the auditory nerve.

It's important to note that any damage or dysfunction in the Scala Tympani or other parts of the inner ear can lead to hearing loss or other auditory disorders.

The temporal bone is a paired bone that is located on each side of the skull, forming part of the lateral and inferior walls of the cranial cavity. It is one of the most complex bones in the human body and has several important structures associated with it. The main functions of the temporal bone include protecting the middle and inner ear, providing attachment for various muscles of the head and neck, and forming part of the base of the skull.

The temporal bone is divided into several parts, including the squamous part, the petrous part, the tympanic part, and the styloid process. The squamous part forms the lateral portion of the temporal bone and articulates with the parietal bone. The petrous part is the most medial and superior portion of the temporal bone and contains the inner ear and the semicircular canals. The tympanic part forms the lower and anterior portions of the temporal bone and includes the external auditory meatus or ear canal. The styloid process is a long, slender projection that extends downward from the inferior aspect of the temporal bone and serves as an attachment site for various muscles and ligaments.

The temporal bone plays a crucial role in hearing and balance, as it contains the structures of the middle and inner ear, including the oval window, round window, cochlea, vestibule, and semicircular canals. The stapes bone, one of the three bones in the middle ear, is entirely encased within the petrous portion of the temporal bone. Additionally, the temporal bone contains important structures for facial expression and sensation, including the facial nerve, which exits the skull through the stylomastoid foramen, a small opening in the temporal bone.

I must clarify that the term "Guinea Pigs" is not typically used in medical definitions. However, in colloquial or informal language, it may refer to people who are used as the first to try out a new medical treatment or drug. This is known as being a "test subject" or "in a clinical trial."

In the field of scientific research, particularly in studies involving animals, guinea pigs are small rodents that are often used as experimental subjects due to their size, cost-effectiveness, and ease of handling. They are not actually pigs from Guinea, despite their name's origins being unclear. However, they do not exactly fit the description of being used in human medical experiments.

"CBA" is an abbreviation for a specific strain of inbred mice that were developed at the Cancer Research Institute in London. The "Inbred CBA" mice are genetically identical individuals within the same strain, due to many generations of brother-sister matings. This results in a homozygous population, making them valuable tools for research because they reduce variability and increase reproducibility in experimental outcomes.

The CBA strain is known for its susceptibility to certain diseases, such as autoimmune disorders and cancer, which makes it a popular choice for researchers studying those conditions. Additionally, the CBA strain has been widely used in studies related to transplantation immunology, infectious diseases, and genetic research.

It's important to note that while "Inbred CBA" mice are a well-established and useful tool in biomedical research, they represent only one of many inbred strains available for scientific investigation. Each strain has its own unique characteristics and advantages, depending on the specific research question being asked.

Afferent neurons, also known as sensory neurons, are a type of nerve cell that conducts impulses or signals from peripheral receptors towards the central nervous system (CNS), which includes the brain and spinal cord. These neurons are responsible for transmitting sensory information such as touch, temperature, pain, sound, and light to the CNS for processing and interpretation. Afferent neurons have specialized receptor endings that detect changes in the environment and convert them into electrical signals, which are then transmitted to the CNS via synapses with other neurons. Once the signals reach the CNS, they are processed and integrated with other information to produce a response or reaction to the stimulus.

Nerve Growth Factors (NGFs) are a family of proteins that play an essential role in the growth, maintenance, and survival of certain neurons (nerve cells). They were first discovered by Rita Levi-Montalcini and Stanley Cohen in 1956. NGF is particularly crucial for the development and function of the peripheral nervous system, which connects the central nervous system to various organs and tissues throughout the body.

NGF supports the differentiation and survival of sympathetic and sensory neurons during embryonic development. In adults, NGF continues to regulate the maintenance and repair of these neurons, contributing to neuroplasticity – the brain's ability to adapt and change over time. Additionally, NGF has been implicated in pain transmission and modulation, as well as inflammatory responses.

Abnormal levels or dysfunctional NGF signaling have been associated with various medical conditions, including neurodegenerative diseases (e.g., Alzheimer's and Parkinson's), chronic pain disorders, and certain cancers (e.g., small cell lung cancer). Therefore, understanding the role of NGF in physiological and pathological processes may provide valuable insights into developing novel therapeutic strategies for these conditions.

The Stellate Ganglion is a part of the sympathetic nervous system. It's a collection of nerve cells (a ganglion) located in the neck, more specifically at the level of the sixth and seventh cervical vertebrae. The stellate ganglion is formed by the fusion of the inferior cervical ganglion and the first thoracic ganglion.

This ganglion plays a crucial role in the body's "fight or flight" response, providing sympathetic innervation to the head, neck, upper extremities, and heart. It's responsible for various functions including regulation of blood flow, sweat gland activity, and contributing to the sensory innervation of the head and neck.

Stellate ganglion block is a medical procedure used to diagnose or treat certain conditions like pain disorders, by injecting local anesthetic near the stellate ganglion to numb the area and interrupt nerve signals.

Auditory pathways refer to the series of structures and nerves in the body that are involved in processing sound and transmitting it to the brain for interpretation. The process begins when sound waves enter the ear and cause vibrations in the eardrum, which then move the bones in the middle ear. These movements stimulate hair cells in the cochlea, a spiral-shaped structure in the inner ear, causing them to release neurotransmitters that activate auditory nerve fibers.

The auditory nerve carries these signals to the brainstem, where they are relayed through several additional structures before reaching the auditory cortex in the temporal lobe of the brain. Here, the signals are processed and interpreted as sounds, allowing us to hear and understand speech, music, and other environmental noises.

Damage or dysfunction at any point along the auditory pathway can lead to hearing loss or impairment.

An action potential is a brief electrical signal that travels along the membrane of a nerve cell (neuron) or muscle cell. It is initiated by a rapid, localized change in the permeability of the cell membrane to specific ions, such as sodium and potassium, resulting in a rapid influx of sodium ions and a subsequent efflux of potassium ions. This ion movement causes a brief reversal of the electrical potential across the membrane, which is known as depolarization. The action potential then propagates along the cell membrane as a wave, allowing the electrical signal to be transmitted over long distances within the body. Action potentials play a crucial role in the communication and functioning of the nervous system and muscle tissue.

The nodose ganglion is a part of the human autonomic nervous system. It is a collection of nerve cell bodies that are located in the upper neck, near the junction of the skull and the first vertebra (C1). The nodose ganglion is a component of the vagus nerve (cranial nerve X), which is a mixed nerve that carries both sensory and motor fibers.

The sensory fibers in the vagus nerve provide information about the state of the internal organs to the brain, including information about the heart, lungs, and digestive system. The cell bodies of these sensory fibers are located in the nodose ganglion.

The nodose ganglion contains neurons that have cell bodies with long processes called dendrites that extend into the mucous membranes of the respiratory and digestive tracts. These dendrites detect various stimuli, such as mechanical deformation (e.g., stretch), chemical changes (e.g., pH, osmolarity), and temperature changes in the internal environment. The information detected by these dendrites is then transmitted to the brain via the sensory fibers of the vagus nerve.

In summary, the nodose ganglion is a collection of nerve cell bodies that are part of the vagus nerve and provide sensory innervation to the internal organs in the thorax and abdomen.

Acoustic stimulation refers to the use of sound waves or vibrations to elicit a response in an individual, typically for the purpose of assessing or treating hearing, balance, or neurological disorders. In a medical context, acoustic stimulation may involve presenting pure tones, speech sounds, or other types of auditory signals through headphones, speakers, or specialized devices such as bone conduction transducers.

The response to acoustic stimulation can be measured using various techniques, including electrophysiological tests like auditory brainstem responses (ABRs) or otoacoustic emissions (OAEs), behavioral observations, or functional imaging methods like fMRI. Acoustic stimulation is also used in therapeutic settings, such as auditory training programs for hearing impairment or vestibular rehabilitation for balance disorders.

It's important to note that acoustic stimulation should be administered under the guidance of a qualified healthcare professional to ensure safety and effectiveness.

Cell survival refers to the ability of a cell to continue living and functioning normally, despite being exposed to potentially harmful conditions or treatments. This can include exposure to toxins, radiation, chemotherapeutic drugs, or other stressors that can damage cells or interfere with their normal processes.

In scientific research, measures of cell survival are often used to evaluate the effectiveness of various therapies or treatments. For example, researchers may expose cells to a particular drug or treatment and then measure the percentage of cells that survive to assess its potential therapeutic value. Similarly, in toxicology studies, measures of cell survival can help to determine the safety of various chemicals or substances.

It's important to note that cell survival is not the same as cell proliferation, which refers to the ability of cells to divide and multiply. While some treatments may promote cell survival, they may also inhibit cell proliferation, making them useful for treating diseases such as cancer. Conversely, other treatments may be designed to specifically target and kill cancer cells, even if it means sacrificing some healthy cells in the process.

Efferent neurons are specialized nerve cells that transmit signals from the central nervous system (CNS), which includes the brain and spinal cord, to effector organs such as muscles or glands. These signals typically result in a response or action, hence the term "efferent," derived from the Latin word "efferre" meaning "to carry away."

Efferent neurons are part of the motor pathway and can be further classified into two types:

1. Somatic efferent neurons: These neurons transmit signals to skeletal muscles, enabling voluntary movements and posture maintenance. They have their cell bodies located in the ventral horn of the spinal cord and send their axons through the ventral roots to innervate specific muscle fibers.
2. Autonomic efferent neurons: These neurons are responsible for controlling involuntary functions, such as heart rate, digestion, respiration, and pupil dilation. They have a two-neuron chain arrangement, with the preganglionic neuron having its cell body in the CNS (brainstem or spinal cord) and synapsing with the postganglionic neuron in an autonomic ganglion near the effector organ. Autonomic efferent neurons can be further divided into sympathetic, parasympathetic, and enteric subdivisions based on their functions and innervation patterns.

In summary, efferent neurons are a critical component of the nervous system, responsible for transmitting signals from the CNS to various effector organs, ultimately controlling and coordinating numerous bodily functions and responses.

The cochlear nucleus is the first relay station in the auditory pathway within the central nervous system. It is a structure located in the lower pons region of the brainstem and receives sensory information from the cochlea, which is the spiral-shaped organ of hearing in the inner ear.

The cochlear nucleus consists of several subdivisions, each with distinct neuronal populations that process different aspects of auditory information. These subdivisions include the anteroventral cochlear nucleus (AVCN), posteroventral cochlear nucleus (PVCN), dorsal cochlear nucleus (DCN), and the granule cell domain.

Neurons in these subdivisions perform various computations on the incoming auditory signals, such as frequency analysis, intensity coding, and sound localization. The output of the cochlear nucleus is then sent via several pathways to higher brain regions for further processing and interpretation, including the inferior colliculus, medial geniculate body, and eventually the auditory cortex.

Damage or dysfunction in the cochlear nucleus can lead to hearing impairments and other auditory processing disorders.

Noise-induced hearing loss (NIHL) is a type of sensorineural hearing loss that occurs due to exposure to harmful levels of noise. The damage can be caused by a one-time exposure to an extremely loud sound or by continuous exposure to lower level sounds over time. NIHL can affect people of all ages and can cause permanent damage to the hair cells in the cochlea, leading to hearing loss, tinnitus (ringing in the ears), and difficulty understanding speech in noisy environments. Prevention measures include avoiding excessive noise exposure, wearing hearing protection, and taking regular breaks from noisy activities.

The vestibulocochlear nerve, also known as the 8th cranial nerve, is responsible for transmitting sound and balance information from the inner ear to the brain. Vestibulocochlear nerve diseases refer to conditions that affect this nerve and can result in hearing loss, vertigo, and balance problems.

These diseases can be caused by various factors, including genetics, infection, trauma, tumors, or degeneration. Some examples of vestibulocochlear nerve diseases include:

1. Vestibular neuritis: an inner ear infection that causes severe vertigo, nausea, and balance problems.
2. Labyrinthitis: an inner ear infection that affects both the vestibular and cochlear nerves, causing vertigo, hearing loss, and tinnitus.
3. Acoustic neuroma: a benign tumor that grows on the vestibulocochlear nerve, causing hearing loss, tinnitus, and balance problems.
4. Meniere's disease: a inner ear disorder that causes vertigo, hearing loss, tinnitus, and a feeling of fullness in the ear.
5. Ototoxicity: damage to the inner ear caused by certain medications or chemicals that can result in hearing loss and balance problems.
6. Vestibular migraine: a type of migraine that is associated with vertigo, dizziness, and balance problems.

Treatment for vestibulocochlear nerve diseases varies depending on the specific condition and its severity. It may include medication, physical therapy, surgery, or a combination of these approaches.

Kanamycin is an aminoglycoside antibiotic that is derived from the bacterium Streptomyces kanamyceticus. It works by binding to the 30S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and leading to bacterial cell death. Kanamycin is primarily used to treat serious infections caused by Gram-negative bacteria, such as Pseudomonas aeruginosa, Escherichia coli, and Klebsiella pneumoniae. It is also used in veterinary medicine to prevent bacterial infections in animals.

Like other aminoglycosides, kanamycin can cause ototoxicity (hearing loss) and nephrotoxicity (kidney damage) with prolonged use or high doses. Therefore, it is important to monitor patients closely for signs of toxicity and adjust the dose accordingly. Kanamycin is not commonly used as a first-line antibiotic due to its potential side effects and the availability of safer alternatives. However, it remains an important option for treating multidrug-resistant bacterial infections.

The vestibular system is a part of the inner ear that contributes to our sense of balance and spatial orientation. It is made up of two main components: the vestibule and the labyrinth.

The vestibule is a bony chamber in the inner ear that contains two important structures called the utricle and saccule. These structures contain hair cells and fluid-filled sacs that help detect changes in head position and movement, allowing us to maintain our balance and orientation in space.

The labyrinth, on the other hand, is a more complex structure that includes the vestibule as well as three semicircular canals. These canals are also filled with fluid and contain hair cells that detect rotational movements of the head. Together, the vestibule and labyrinth work together to provide us with information about our body's position and movement in space.

Overall, the vestibular system plays a crucial role in maintaining our balance, coordinating our movements, and helping us navigate through our environment.

Neomycin is an antibiotic drug derived from the bacterium Streptomyces fradiae. It belongs to the class of aminoglycoside antibiotics and works by binding to the 30S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and leading to bacterial cell death. Neomycin is primarily used topically (on the skin or mucous membranes) due to its poor absorption into the bloodstream when taken orally. It is effective against a wide range of gram-positive and gram-negative bacteria. Medical definitions for Neomycin include:

1. An antibiotic (aminoglycoside) derived from Streptomyces fradiae, used primarily for topical application in the treatment of superficial infections, burns, and wounds. It is not usually used systemically due to its potential ototoxicity and nephrotoxicity.
2. A medication (generic name) available as a cream, ointment, solution, or powder, often combined with other active ingredients such as bacitracin and polymyxin B for broader-spectrum antibacterial coverage. Neomycin is used to treat various skin conditions, including eczema, dermatitis, and minor cuts or abrasions.
3. A component of some over-the-counter products (e.g., ear drops, eye drops) intended for the treatment of external otitis, swimmer's ear, or bacterial conjunctivitis. It is crucial to follow the instructions carefully and avoid using neomycin-containing products for extended periods or in larger quantities than recommended, as this may increase the risk of antibiotic resistance and potential side effects.

In summary, Neomycin is an aminoglycoside antibiotic primarily used topically for treating various superficial bacterial infections due to its effectiveness against a wide range of gram-positive and gram-negative bacteria. It should be used cautiously and as directed to minimize the risk of side effects and antibiotic resistance.

Cochlear microphonic potentials (CMs) are electrical responses that originate from the hair cells in the cochlea, which is a part of the inner ear responsible for hearing. These potentials can be recorded using an electrode placed near the cochlea in response to sound stimulation.

The CMs are considered to be a passive response of the hair cells to the mechanical deflection caused by sound waves. They represent the receptor potential of the outer hair cells and are directly proportional to the sound pressure level. Unlike other electrical responses in the cochlea, such as the action potentials generated by the auditory nerve fibers, CMs do not require the presence of neurotransmitters or synaptic transmission.

Cochlear microphonic potentials have been used in research to study the biophysical properties of hair cells and their response to different types of sound stimuli. However, they are not typically used in clinical audiology due to their small amplitude and susceptibility to interference from other electrical signals in the body.

In invertebrate biology, ganglia are clusters of neurons that function as a centralized nervous system. They can be considered as the equivalent to a vertebrate's spinal cord and brain. Ganglia serve to process sensory information, coordinate motor functions, and integrate various neural activities within an invertebrate organism.

Invertebrate ganglia are typically found in animals such as arthropods (insects, crustaceans), annelids (earthworms), mollusks (snails, squids), and cnidarians (jellyfish). The structure of the ganglia varies among different invertebrate groups.

For example, in arthropods, the central nervous system consists of a pair of connected ganglia called the supraesophageal ganglion or brain, and the subesophageal ganglion, located near the esophagus. The ventral nerve cord runs along the length of the body, containing pairs of ganglia that control specific regions of the body.

In mollusks, the central nervous system is composed of several ganglia, which can be fused or dispersed, depending on the species. In cephalopods (such as squids and octopuses), the brain is highly developed and consists of several lobes that perform various functions, including learning and memory.

Overall, invertebrate ganglia are essential components of the nervous system that allow these animals to respond to environmental stimuli, move, and interact with their surroundings.

"Cat" is a common name that refers to various species of small carnivorous mammals that belong to the family Felidae. The domestic cat, also known as Felis catus or Felis silvestris catus, is a popular pet and companion animal. It is a subspecies of the wildcat, which is found in Europe, Africa, and Asia.

Domestic cats are often kept as pets because of their companionship, playful behavior, and ability to hunt vermin. They are also valued for their ability to provide emotional support and therapy to people. Cats are obligate carnivores, which means that they require a diet that consists mainly of meat to meet their nutritional needs.

Cats are known for their agility, sharp senses, and predatory instincts. They have retractable claws, which they use for hunting and self-defense. Cats also have a keen sense of smell, hearing, and vision, which allow them to detect prey and navigate their environment.

In medical terms, cats can be hosts to various parasites and diseases that can affect humans and other animals. Some common feline diseases include rabies, feline leukemia virus (FeLV), feline immunodeficiency virus (FIV), and toxoplasmosis. It is important for cat owners to keep their pets healthy and up-to-date on vaccinations and preventative treatments to protect both the cats and their human companions.

Immunohistochemistry (IHC) is a technique used in pathology and laboratory medicine to identify specific proteins or antigens in tissue sections. It combines the principles of immunology and histology to detect the presence and location of these target molecules within cells and tissues. This technique utilizes antibodies that are specific to the protein or antigen of interest, which are then tagged with a detection system such as a chromogen or fluorophore. The stained tissue sections can be examined under a microscope, allowing for the visualization and analysis of the distribution and expression patterns of the target molecule in the context of the tissue architecture. Immunohistochemistry is widely used in diagnostic pathology to help identify various diseases, including cancer, infectious diseases, and immune-mediated disorders.

Gerbillinae is a subfamily of rodents that includes gerbils, jirds, and sand rats. These small mammals are primarily found in arid regions of Africa and Asia. They are characterized by their long hind legs, which they use for hopping, and their long, thin tails. Some species have adapted to desert environments by developing specialized kidneys that allow them to survive on minimal water intake.

Electric stimulation, also known as electrical nerve stimulation or neuromuscular electrical stimulation, is a therapeutic treatment that uses low-voltage electrical currents to stimulate nerves and muscles. It is often used to help manage pain, promote healing, and improve muscle strength and mobility. The electrical impulses can be delivered through electrodes placed on the skin or directly implanted into the body.

In a medical context, electric stimulation may be used for various purposes such as:

1. Pain management: Electric stimulation can help to block pain signals from reaching the brain and promote the release of endorphins, which are natural painkillers produced by the body.
2. Muscle rehabilitation: Electric stimulation can help to strengthen muscles that have become weak due to injury, illness, or surgery. It can also help to prevent muscle atrophy and improve range of motion.
3. Wound healing: Electric stimulation can promote tissue growth and help to speed up the healing process in wounds, ulcers, and other types of injuries.
4. Urinary incontinence: Electric stimulation can be used to strengthen the muscles that control urination and reduce symptoms of urinary incontinence.
5. Migraine prevention: Electric stimulation can be used as a preventive treatment for migraines by applying electrical impulses to specific nerves in the head and neck.

It is important to note that electric stimulation should only be administered under the guidance of a qualified healthcare professional, as improper use can cause harm or discomfort.

The superior cervical ganglion is a part of the autonomic nervous system, specifically the sympathetic division. It is a collection of nerve cell bodies (ganglion) that are located in the neck region (cervical) and is formed by the fusion of several smaller ganglia.

This ganglion is responsible for providing innervation to various structures in the head and neck, including the eyes, scalp, face muscles, meninges (membranes surrounding the brain and spinal cord), and certain glands such as the salivary and sweat glands. It does this through the postganglionic fibers that branch off from the ganglion and synapse with target organs or tissues.

The superior cervical ganglion is an essential component of the autonomic nervous system, which controls involuntary physiological functions such as heart rate, blood pressure, digestion, and respiration.

Sensory receptor cells are specialized structures that convert physical stimuli from our environment into electrical signals, which are then transmitted to the brain for interpretation. These receptors can be found in various tissues throughout the body and are responsible for detecting sensations such as touch, pressure, temperature, taste, and smell. They can be classified into two main types: exteroceptors, which respond to stimuli from the external environment, and interoceptors, which react to internal conditions within the body. Examples of sensory receptor cells include hair cells in the inner ear, photoreceptors in the eye, and taste buds on the tongue.

Schwann cells, also known as neurolemmocytes, are a type of glial cell that form the myelin sheath around peripheral nervous system (PNS) axons, allowing for the rapid and efficient transmission of nerve impulses. These cells play a crucial role in the maintenance and function of the PNS.

Schwann cells originate from the neural crest during embryonic development and migrate to the developing nerves. They wrap around the axons in a spiral fashion, forming multiple layers of myelin, which insulates the nerve fibers and increases the speed of electrical impulse transmission. Each Schwann cell is responsible for myelinating a single segment of an axon, with the gaps between these segments called nodes of Ranvier.

Schwann cells also provide structural support to the neurons and contribute to the regeneration of injured peripheral nerves by helping to guide the regrowth of axons to their targets. Additionally, Schwann cells can participate in immune responses within the PNS, such as releasing cytokines and chemokines to recruit immune cells during injury or infection.

Nerve tissue proteins are specialized proteins found in the nervous system that provide structural and functional support to nerve cells, also known as neurons. These proteins include:

1. Neurofilaments: These are type IV intermediate filaments that provide structural support to neurons and help maintain their shape and size. They are composed of three subunits - NFL (light), NFM (medium), and NFH (heavy).

2. Neuronal Cytoskeletal Proteins: These include tubulins, actins, and spectrins that provide structural support to the neuronal cytoskeleton and help maintain its integrity.

3. Neurotransmitter Receptors: These are specialized proteins located on the postsynaptic membrane of neurons that bind neurotransmitters released by presynaptic neurons, triggering a response in the target cell.

4. Ion Channels: These are transmembrane proteins that regulate the flow of ions across the neuronal membrane and play a crucial role in generating and transmitting electrical signals in neurons.

5. Signaling Proteins: These include enzymes, receptors, and adaptor proteins that mediate intracellular signaling pathways involved in neuronal development, differentiation, survival, and death.

6. Adhesion Proteins: These are cell surface proteins that mediate cell-cell and cell-matrix interactions, playing a crucial role in the formation and maintenance of neural circuits.

7. Extracellular Matrix Proteins: These include proteoglycans, laminins, and collagens that provide structural support to nerve tissue and regulate neuronal migration, differentiation, and survival.

Nerve regeneration is the process of regrowth and restoration of functional nerve connections following damage or injury to the nervous system. This complex process involves various cellular and molecular events, such as the activation of support cells called glia, the sprouting of surviving nerve fibers (axons), and the reformation of neural circuits. The goal of nerve regeneration is to enable the restoration of normal sensory, motor, and autonomic functions impaired due to nerve damage or injury.

Electrophysiological phenomena refer to the electrical properties and activities of biological tissues, cells, or organ systems, particularly in relation to nerve and muscle function. These phenomena can be studied using various techniques such as electrocardiography (ECG), electromyography (EMG), and electroencephalography (EEG).

In the context of cardiology, electrophysiological phenomena are often used to describe the electrical activity of the heart. The ECG is a non-invasive test that measures the electrical activity of the heart as it contracts and relaxes. By analyzing the patterns of electrical activity, doctors can diagnose various heart conditions such as arrhythmias, myocardial infarction, and electrolyte imbalances.

In neurology, electrophysiological phenomena are used to study the electrical activity of the brain. The EEG is a non-invasive test that measures the electrical activity of the brain through sensors placed on the scalp. By analyzing the patterns of electrical activity, doctors can diagnose various neurological conditions such as epilepsy, sleep disorders, and brain injuries.

Overall, electrophysiological phenomena are an important tool in medical diagnostics and research, providing valuable insights into the function of various organ systems.

Basal ganglia diseases are a group of neurological disorders that affect the function of the basal ganglia, which are clusters of nerve cells located deep within the brain. The basal ganglia play a crucial role in controlling movement and coordination. When they are damaged or degenerate, it can result in various motor symptoms such as tremors, rigidity, bradykinesia (slowness of movement), and difficulty with balance and walking.

Some examples of basal ganglia diseases include:

1. Parkinson's disease - a progressive disorder that affects movement due to the death of dopamine-producing cells in the basal ganglia.
2. Huntington's disease - an inherited neurodegenerative disorder that causes uncontrolled movements, emotional problems, and cognitive decline.
3. Dystonia - a movement disorder characterized by sustained or intermittent muscle contractions that cause twisting and repetitive movements or abnormal postures.
4. Wilson's disease - a rare genetic disorder that causes excessive copper accumulation in the liver and brain, leading to neurological and psychiatric symptoms.
5. Progressive supranuclear palsy (PSP) - a rare brain disorder that affects movement, gait, and balance, as well as speech and swallowing.
6. Corticobasal degeneration (CBD) - a rare neurological disorder characterized by progressive loss of nerve cells in the cerebral cortex and basal ganglia, leading to stiffness, rigidity, and difficulty with movement and coordination.

Treatment for basal ganglia diseases varies depending on the specific diagnosis and symptoms but may include medication, surgery, physical therapy, or a combination of these approaches.

"Cell count" is a medical term that refers to the process of determining the number of cells present in a given volume or sample of fluid or tissue. This can be done through various laboratory methods, such as counting individual cells under a microscope using a specialized grid called a hemocytometer, or using automated cell counters that use light scattering and electrical impedance techniques to count and classify different types of cells.

Cell counts are used in a variety of medical contexts, including hematology (the study of blood and blood-forming tissues), microbiology (the study of microscopic organisms), and pathology (the study of diseases and their causes). For example, a complete blood count (CBC) is a routine laboratory test that includes a white blood cell (WBC) count, red blood cell (RBC) count, hemoglobin level, hematocrit value, and platelet count. Abnormal cell counts can indicate the presence of various medical conditions, such as infections, anemia, or leukemia.

"Cells, cultured" is a medical term that refers to cells that have been removed from an organism and grown in controlled laboratory conditions outside of the body. This process is called cell culture and it allows scientists to study cells in a more controlled and accessible environment than they would have inside the body. Cultured cells can be derived from a variety of sources, including tissues, organs, or fluids from humans, animals, or cell lines that have been previously established in the laboratory.

Cell culture involves several steps, including isolation of the cells from the tissue, purification and characterization of the cells, and maintenance of the cells in appropriate growth conditions. The cells are typically grown in specialized media that contain nutrients, growth factors, and other components necessary for their survival and proliferation. Cultured cells can be used for a variety of purposes, including basic research, drug development and testing, and production of biological products such as vaccines and gene therapies.

It is important to note that cultured cells may behave differently than they do in the body, and results obtained from cell culture studies may not always translate directly to human physiology or disease. Therefore, it is essential to validate findings from cell culture experiments using additional models and ultimately in clinical trials involving human subjects.

Pure-tone audiometry is a hearing test that measures a person's ability to hear different sounds, pitches, or frequencies. During the test, pure tones are presented to the patient through headphones or ear inserts, and the patient is asked to indicate each time they hear the sound by raising their hand, pressing a button, or responding verbally.

The softest sound that the person can hear at each frequency is recorded as the hearing threshold, and a graph called an audiogram is created to show the results. The audiogram provides information about the type and degree of hearing loss in each ear. Pure-tone audiometry is a standard hearing test used to diagnose and monitor hearing disorders.

Animal disease models are specialized animals, typically rodents such as mice or rats, that have been genetically engineered or exposed to certain conditions to develop symptoms and physiological changes similar to those seen in human diseases. These models are used in medical research to study the pathophysiology of diseases, identify potential therapeutic targets, test drug efficacy and safety, and understand disease mechanisms.

The genetic modifications can include knockout or knock-in mutations, transgenic expression of specific genes, or RNA interference techniques. The animals may also be exposed to environmental factors such as chemicals, radiation, or infectious agents to induce the disease state.

Examples of animal disease models include:

1. Mouse models of cancer: Genetically engineered mice that develop various types of tumors, allowing researchers to study cancer initiation, progression, and metastasis.
2. Alzheimer's disease models: Transgenic mice expressing mutant human genes associated with Alzheimer's disease, which exhibit amyloid plaque formation and cognitive decline.
3. Diabetes models: Obese and diabetic mouse strains like the NOD (non-obese diabetic) or db/db mice, used to study the development of type 1 and type 2 diabetes, respectively.
4. Cardiovascular disease models: Atherosclerosis-prone mice, such as ApoE-deficient or LDLR-deficient mice, that develop plaque buildup in their arteries when fed a high-fat diet.
5. Inflammatory bowel disease models: Mice with genetic mutations affecting intestinal barrier function and immune response, such as IL-10 knockout or SAMP1/YitFc mice, which develop colitis.

Animal disease models are essential tools in preclinical research, but it is important to recognize their limitations. Differences between species can affect the translatability of results from animal studies to human patients. Therefore, researchers must carefully consider the choice of model and interpret findings cautiously when applying them to human diseases.

The inferior colliculi are a pair of rounded eminences located in the midbrain, specifically in the tectum of the mesencephalon. They play a crucial role in auditory processing and integration. The inferior colliculi receive inputs from various sources, including the cochlear nuclei, superior olivary complex, and cortical areas. They then send their outputs to the medial geniculate body, which is a part of the thalamus that relays auditory information to the auditory cortex.

In summary, the inferior colliculi are important structures in the auditory pathway that help process and integrate auditory information before it reaches the cerebral cortex for further analysis and perception.

Tinnitus is the perception of ringing or other sounds in the ears or head when no external sound is present. It can be described as a sensation of hearing sound even when no actual noise is present. The sounds perceived can vary widely, from a whistling, buzzing, hissing, swooshing, to a pulsating sound, and can be soft or loud.

Tinnitus is not a disease itself but a symptom that can result from a wide range of underlying causes, such as hearing loss, exposure to loud noises, ear infections, earwax blockage, head or neck injuries, circulatory system disorders, certain medications, and age-related hearing loss.

Tinnitus can be temporary or chronic, and it may affect one or both ears. While tinnitus is not usually a sign of a serious medical condition, it can significantly impact quality of life and interfere with daily activities, sleep, and concentration.

Spontaneous otoacoustic emissions (SOAEs) are low-level sounds that are produced by the inner ear (cochlea) without any external stimulation. They can be recorded in a quiet room using specialized microphones placed inside the ear canal. SOAEs are thought to arise from the motion of the hair cells within the cochlea, which generate tiny currents in response to sound. These currents then cause the surrounding fluid and tissue to vibrate, producing sound waves that can be detected with a microphone.

SOAEs are typically present in individuals with normal hearing, although their presence or absence is not a definitive indicator of hearing ability. They tend to occur at specific frequencies and can vary from person to person. In some cases, SOAEs may be absent or reduced in individuals with hearing loss or damage to the hair cells in the cochlea.

It's worth noting that SOAEs are different from evoked otoacoustic emissions (EOAEs), which are sounds produced by the inner ear in response to external stimuli, such as clicks or tones. Both types of otoacoustic emissions are used in hearing tests and research to assess cochlear function and health.

The spiral lamina is a bony structure within the inner ear, specifically located in the cochlea. It is a part of the osseous labyrinth and plays a crucial role in the process of hearing. The spiral lamina arises from the modiolus, which is the central axis of the cochlea, and it spirals upward as it extends toward the outer wall of the cochlear duct.

The spiral lamina supports the organ of Corti, which contains hair cells responsible for converting sound vibrations into electrical signals that are transmitted to the brain via the auditory nerve. Additionally, the spiral lamina helps in maintaining the separation between the Scala Media (containing the cochlear duct) and Scala Tympani (one of the three fluid-filled channels within the cochlea).

In summary, the spiral lamina is a vital component of the inner ear's anatomy, providing structural support to the organ of Corti and contributing to the proper functioning of the auditory system.

Neurogenesis is the process by which new neurons (nerve cells) are generated in the brain. It occurs throughout life in certain areas of the brain, such as the hippocampus and subventricular zone, although the rate of neurogenesis decreases with age. Neurogenesis involves the proliferation, differentiation, and integration of new neurons into existing neural circuits. This process plays a crucial role in learning, memory, and recovery from brain injury or disease.

Two apparent subtypes of spiral ganglion cells exist. Type I spiral ganglion cells comprise the vast majority of spiral ... the vestibular ganglion and the spiral ganglion. The axons of neurons in the spiral ganglion travel to the brainstem, forming ... Type II spiral ganglion cells make up the remainder. In contrast to Type I cells, they are unipolar and unmyelinated in most ... The spiral (cochlear) ganglion is a group of neuron cell bodies in the modiolus, the conical central axis of the cochlea. These ...
Neural: characterised by degeneration of cells of the spiral ganglion. Strial/metabolic: characterised by atrophy of stria ... GPx1, an isoform of GPx, is predominantly expressed in stria vascularis, cochlea, spiral ligament, organ of Corti, and spiral ... in CD4+ T cells and degeneration of the spiral ganglion in Samp1 mice, a murine model of human senescence. This technology ... The cochlea is tonotopically mapped in a spiral fashion, with lower frequencies localizing at the apex of the cochlea, and high ...
"Analog transmission of action potential fine structure in spiral ganglion axons". Journal of Neurophysiology. 126 (3): 888-905 ... the ganglion cells, produce action potentials, which then travel up the optic nerve. In sensory neurons, action potentials ...
The cochlear nerve, as well as spiral ganglion is situated inside it. The cochlear nerve conducts impulses from the receptors ... The modiolus is not labeled; it's at the axis of the spiral of the cochlea. Modiolus (disambiguation) This article incorporates ...
Optogenetic application onto the cochlear region allows for the stimulation or inhibition of the spiral ganglion cells (SGN). ... Optogenetic stimulation of the spiral ganglion in deaf mice restored auditory activity. ... Zhuo-Hua Pan of Wayne State University, researching on restore sight to blindness, tried channelrhodopsin out in ganglion cells ... Optogenetics was applied on atrial cardiomyocytes to end spiral wave arrhythmias, found to occur in atrial fibrillation, with ...
This protective agent was also found to be associated with survival of cochlear spiral ganglion neurones after hearing loss or ... Leake, Patricia A.; Akil, Omar; Lang, Hainan (2020). "Neurotrophin gene therapy to promote survival of spiral ganglion neurons ...
August 2013). "Protection of spiral ganglion neurons from degeneration using small-molecule TrkB receptor agonists". The ... protects spiral ganglion neurons from degeneration both in vitro and in vivo". Biochemical and Biophysical Research ...
These regenerated hair cell-like cells likely form connections with adult spiral ganglion neurons. Myc and Notch 1 co- ...
The cochlear nerve travels away from the cochlea of the inner ear where it starts as the spiral ganglia. Processes from the ... The vestibular ganglion houses the cell bodies of the bipolar neurons and extends processes to five sensory organs. Three of ... organ of Corti conduct afferent transmission to the spiral ganglia. It is the inner hair cells of the organ of Corti that are ...
"Effects of Quinine on the Excitability and Voltage-Dependent Currents of Isolated Spiral Ganglion Neurons in Culture". Journal ...
When a certain threshold potential is reached, the spiral ganglion neuron fires an action potential, which enters the auditory ... The depolarized hair cell releases neurotransmitters across a synapse to primary auditory neurons of the spiral ganglion. Upon ... reaching receptors on the postsynaptic spiral ganglion neurons, the neurotransmitters induce a postsynaptic potential or ...
Hyperpolarization causes less calcium influx, thus less neurotransmitter release, and a reduced probability of spiral ganglion ... Spiral limbus and basilar membrane. Section through the spiral organ of Corti (magnified) The reticular membrane and subjacent ... acting on the spiral ganglion cell, the primary auditory neurons, making them more likely to spike. ...
The post-synaptic neurite then sends an action potential to the Spiral Ganglia of Gard. Unlike the hair cells of the crista ...
Beisel KW, Nelson NC, Delimont DC, Fritzsch B (2001). "Longitudinal gradients of KCNQ4 expression in spiral ganglion and ...
It has also been proposed and then refuted at the ribbon synapses formed between inner hair cell and spiral ganglion neurons. ...
Specialized inner ear cell include: hair cells, pillar cells, Boettcher's cells, Claudius' cells, spiral ganglion neurons, and ... the central axis of the cochlea that contains the spiral ganglion. ... Rosenthal's canal or the spiral canal of the cochlea is a section of the bony labyrinth of the inner ear that is approximately ... The lateral wall of the cochlear duct is formed by the spiral ligament and the stria vascularis, which produces the endolymph. ...
The outer hair cells (OHC) are minimally innervated by spiral ganglion in slow (unmyelinated) reciprocal communicative bundles ...
It was found that some months after the organ of Corti had degenerated, the spiral ganglion of the cochlea also began to ...
Axons from the spiral ganglion cells of the lower frequencies innervate the ventrolateral portions of the ventral cochlear ... Each fiber is an axon of a spiral ganglion cell that represents a particular frequency of sound, and a particular range of ... trigeminal ganglion and nucleus, dorsal column nuclei and the second dorsal root ganglion. It is likely that these neurons help ... organization is preserved because only a few inner hair cells synapse on the dendrites of a nerve cell in the spiral ganglion, ...
While the vestibulocochlear nerve has two ganglia associated with it (spiral ganglion and vestibular ganglion), both contain ... Specifically the: trigeminal ganglion geniculate ganglion superior ganglion of the glossopharyngeal nerve inferior ganglion of ... Pseudounipolar neurons in the geniculate ganglion, inferior ganglion of the glossopharyngeal nerve and inferior ganglion of the ... The ones found in the dorsal root ganglia, and majority of those in cranial nerve sensory ganglia carry information about touch ...
... deletion also impairs auditory function because of the loss of regulation of Kv4.2 channels by KCNE3 in spiral ganglion ...
The cell bodies of the cochlear nerve lie within the cochlea and collectively form the spiral ganglion, named for the spiral ...
... which encodes a half-wave rectified signal of action potentials in the spiral ganglion cells. The axons of these cells make up ...
... developing cochlea generate bursts of activity which spreads across the inner hair cells and spiral ganglion neurons which ... Meister, M; Wong, R.O.L; Baylor, D.A; Shatz, C.J (1991). "Synchronous bursts of action potentials in ganglion cells of the ... In the immature retina, waves of spontaneous action potentials arise from the retinal ganglion cells and sweep across the ... Jones, T.A; Jones, S.M; Paggett, K.C (15 October 2001). "Primordial rhythmic bursting in embryonic cochlear ganglion cells". ...
... whose first-order neurons have already synapsed at the spiral ganglion) to proceed towards the CNS as a single unified ... The vestibular ganglion (also called Scarpa's ganglion) is a ganglion situated within the internal auditory meatus that lodges ... The superior division and inferior division of the vestibular nerve meet at the ganglion; henceforth, the fibres of second- ... ISBN 978-0-7295-3752-0. Sato H; Sando I; Takahashi H (September 1992). "Three-dimensional anatomy of human Scarpa's ganglion". ...
... into the blood stream Cells of the sympathetic ganglia Cells of the parasympathetic ganglia Cells of the spiral ganglia ( ... A ganglion cell is a cell found in a ganglion. Examples of ganglion cells include: Retinal ganglion cell (RGC) found in the ... ganglion cell layer of the retina Cells that reside in the adrenal medulla, where they are involved in the sympathetic nervous ...
... contains unmyelinated fibres that synapse with the dendrites of the Type I spiral ganglion cells projecting to the inner hair ... In comparison, shell neurons spiral both apically and basally, and can cover large territories within the organ of Corti. The ... Intrinsic LOCS derived axons travel only approximately 1 µm within the organ of Corti, generally spiraling apically. They give ...
... of the scapula spinocerebellar tract spinocerebellum spinocervical pathway spinothalamic tract spinous process spiral ganglion ... reflex galea aponeurotica gall bladder gamma motoneurons ganglion ganglion cell ganglion cell of the retina gasserian ganglion ... costal margin costophrenic angle Cowper's gland coxae cranial cranial autonomic ganglia cranial bone cranial nerve ganglia ... cervical plexus cervical spinal nerves cervical spine cervical sympathetic ganglia cervical vertebrae cervicothoracic ganglion ...
... illustrating its role in anxious behavior and ASIC3 has been found in the organ of Corti and spiral ganglion illustrating this ...
... and send their signals via neurotransmitter to the primary auditory neurons of the spiral ganglion. The hair cells in the Organ ... The name cochlea derives from Ancient Greek κοχλίας (kokhlias) 'spiral, snail shell'. The cochlea (PL: cochleae) is a spiraled ... the top or center of the spiral). The spiral canal of the cochlea is a section of the bony labyrinth of the inner ear that is ... It is a spiral-shaped cavity in the bony labyrinth, in humans making 2.75 turns around its axis, the modiolus. A core component ...
Two apparent subtypes of spiral ganglion cells exist. Type I spiral ganglion cells comprise the vast majority of spiral ... the vestibular ganglion and the spiral ganglion. The axons of neurons in the spiral ganglion travel to the brainstem, forming ... Type II spiral ganglion cells make up the remainder. In contrast to Type I cells, they are unipolar and unmyelinated in most ... The spiral (cochlear) ganglion is a group of neuron cell bodies in the modiolus, the conical central axis of the cochlea. These ...
Effect of Tissue Heterogeneity on the Transmembrane Potential of Type-1 Spiral Ganglion Neurons: A Simulation Study. * February ... Electric field applied by cochlear implants stimulates the intact type-1 spiral ganglion neurons (SGNs) in the Rosenthals ... Effect of Tissue Heterogeneity on the Transmembrane Potential of Type-1 Spiral Ganglion Neurons: A Simulation Study https://www ...
3.58 spiral ganglion of the cochlea. Cell bodies of the neurons of the cochlear nerve, located within the modiolus. The ...
... spiral ganglion; SL, spiral ligament; SM, scala media; SP, spiral prominence; ST, scala tympani; StV, stria vascularis; SV, ... Cochlear expression patterns of GJB2 BM, basilar membrane; BSL, bony spiral lamina; CC, Claudius cell; DC, Deiters cell; ESC, ...
SNHL is caused by the irreversible loss of sensory hair cell and the degeneration of spiral ganglion neurons. SNHL is not yet ... Special Issue "Hair Cell and Spiral Ganglion Neuron Regeneration: Mechanisms, Cure and Future Prospects" * Special Issue ... Neural plasticity is the key feature for spiral ganglion neurons and hair cells, and is especially important for the new ... This Special Issue will focus on recent advances in re-establishing the neural plasticity of regenerated spiral ganglion ...
Ptf1a expression is necessary for correct targeting of spiral ganglion neurons within the cochlear nuclei. Karen L Elliott, ... Ptf1a expression is necessary for correct targeting of spiral ganglion neurons within the cochlear nuclei. Neuroscience letters ...
... exhibit apparently complementary expression patterns in the spiral ganglion and its nearby region, the spiral limbus. In Slit2 ... exhibit apparently complementary expression patterns in the spiral ganglion and its nearby region, the spiral limbus. In Slit2 ... exhibit apparently complementary expression patterns in the spiral ganglion and its nearby region, the spiral limbus. In Slit2 ... exhibit apparently complementary expression patterns in the spiral ganglion and its nearby region, the spiral limbus. In Slit2 ...
Reestablishing Neural Plasticity in Regenerated Spiral Ganglion Neurons and Sensory Hair Cells for Hearing Loss 2020. View this ... "Wnt signaling activates TP53-induced glycolysis and apoptosis regulator and protects against cisplatin-induced spiral ganglion ...
Otic Organoids Containing Spiral Ganglion Neuron-like Cells Derived from Human-induced Pluripotent Stem Cells as a Model of ... The spiral ganglion of the cochlea is essential for hearing and contains primary bipolar neurons that relay action potentials ... Otic Organoids Containing Spiral Ganglion Neuron-like Cells Derived from Human-induced Pluripotent Stem Cells as a Model of ... Otic Organoids Containing Spiral Ganglion Neuron-like Cells Derived from Human-induced Pluripotent Stem Cells as a Model of ...
Specifically, the spiral ganglion cells, auditory nerve, and auditory brainstem nuclei have all been implicated. The ... Although the diagnostic testing results were similar to those found in patients with AN/AD, the destruction of spiral ganglion ... This animal model shows the direct destruction of the spiral ganglion cells and produces the same constellation of symptoms ... Injury to the synaptic junction between inner hair cells of the cochlea and dendrites of spiral ganglion neurons ...
2009). Promoting neurite outgrowth from spiral ganglion neuron explants using polypyrrole/BDNF-coated electrodes. J. Biomed. ... spiral ganglion cells (Evans et al., 2009) and pheochromocytoma (PC12) neural model cells (Schmidt et al., 1997; Green et al., ... maintained spiral ganglion neurons for 28 days through BDNF administration via a mini-osmotic pump. It was expected that this ...
"The Dynamic Spiral Ganglion". Robin Davis (Rutgers University). Host: Alex Markowitz, Grad. Student (HCN) ... Basal Ganglia Circuit Dysfunction Underlying Parkinsons Disease and Dyskinesia. Anatol Kreitzer (UC, San Francisco) Host: ... "The Spiral Staircase: Tonotopic Microstructure and Cochlear Tuning". Christopher Shera (Harvard University). Host: Amanda ... The Basal Ganglia and Behavioral Control. Joshua Berke (University of Michigan). Host: Bottjer (NB) ...
The Molecular and Morphological Development of Spiral Ganglion Neurons. Advisor: Lisa Goodrich. ... Structure and Development of Retinal Ganglion Cells. Advisor: Joshua Sanes. Knoll, Allison. Role of Kappa Opioid Receptors in ... Basal Ganglia Circuitry Controlling Action Selection. Advisor: Bernardo Sabatini. Patella, Paola. Mechanosensory ... Circuit interactions between the cortex and basal ganglia. Advisor: Bernardo Sabatini. Stoppel, David. Social Behavior and Gene ...
TMT preferentially damaged auditory nerve fibers and spiral ganglion neurons in a dose-dependent manner, but had no noticeable ...
Figure created using data from [63] (SGN-spiral ganglion neurons; IHC-inner hair cells; OHC-outer hair cells; VNO-vomeronasal ... Figure created using data from [63] (SGN-spiral ganglion neurons; IHC-inner hair cells; OHC-outer hair cells; VNO-vomeronasal ... During normal (wild-type) development, EphA4 expression was detected in type I spiral ganglion neurons (SGNs), while ephrin-A5 ... Fawcett, J.W.; OLeary, D.D.; Cowan, W.M. Activity and the control of ganglion cell death in the rat retina. Proc. Natl. Acad. ...
Expression of EFR3A in the mouse cochlea during degeneration of spiral ganglion following hair cell loss. Nie C, et al. PLoS ... Efr3a Insufficiency Attenuates the Degeneration of Spiral Ganglion Neurons after Hair Cell Loss. Hu H, et al. Front Mol ... High expression of EFR3A may be important to prompt initiation of spiral ganglion degeneration following hair cell loss. Title ... Study suggests that down-regulation of Efr3a might improve hearing function and alleviate the degeneration of spiral ganglion ...
E. Brunet - Unravelling the mechanisms underlying ultrasound stimulation of dorsal root and spiral ganglion neurons. Keywords ...
The shape of the HiFocus Mid-Scala places the electrode within the scala tympani, close to the spiral ganglion cells for ... Current Steering allows to stimulate the Spiral Ganglion cell population between electrode contacts. ... insertion depth signifying coverage of main Spiral Ganglion cell population23 with a tight standard deviation of 20.7°. ... covering the main spiral ganglion population12 to provide optimal spectral coverage. ...
2009) Distribution of the Na, K-ATPase alpha subunit in the rat spiral ganglion and organ of corti. J Assoc Res Otolaryngol 10: ... 2012) Spike encoding of neurotransmitter release timing by spiral ganglion neurons of the cochlea. J Neurosci 32:4773-4789, doi ... along with the utricle and Scarpas ganglion (SG; A1). Using DIC optics, calyces in the central zone were visualized as bright ... nerve fibers and Scarpas ganglion (Fig. 1A1). Recordings were performed from the central zone of the crista at postnatal days ...
2012) Spike encoding of neurotransmitter release timing by spiral ganglion neurons of the cochlea. J Neurosci 32:4773-4789. doi ...
Apoptosis-inducing factor and calpain up regulation in glutamate-induced injury of rat spiral ganglion neurons. Mol. Med. Rep. ...
Spontaneous discharge patterns in cochlear spiral ganglion cells before the onset of hearing in cats. J. Neurophysiol. 98, 1898 ... Maffei, L., and Galli-Resta, L. (1990). Correlation in the discharges of neighboring rat retinal ganglion cells during prenatal ...
Spiral Ganglion Neuron Explantation Culture et électrophysiologie surmulti-électrodes Arrays… * Préparation et Immunostaining ... Racine Dorsale Ganglion Injection et Racine Dorsale Crush blessures comme modèle pour la régénération sensorielle Axon… ... Racine Dorsale Ganglion Injection et Racine Dorsale Crush blessures comme modèle pour la régénération sensorielle Axon… ... Chargée de lenquête la régénération axonale mammifères : In Vivooration du Ganglion de la racine dorsale de souris adulte… ...
Hearing requires an optimal afferent innervation of sensory hair cells by spiral ganglion neurons in the cochlea. Here we ... report that complementary expression of ephrin-A5 in hair cells and EphA4 receptor among spiral ganglion neuron populations ...
Summary: Info on spiral ganglion sought, Dr L S Smith (Staff). *ICAD Submission Address, Kramer ...
Evidence suggests that the virus may attack the spiral and vestibular ganglion in addition to the cochlear and vestibular ...
... explains the spiral ganglions anatomy, development, and connection to hearing loss in this video from NIDCDs 2020 ... Thomas Coate, Ph.D., explains the spiral ganglions anatomy, development, and connection to hearing loss in this video from ... explains the spiral ganglions anatomy, development, and connection to hearing loss in this video from NIDCDs ,a href="https ...

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