Callithrix
Callitrichinae
Monkey Diseases
Saguinus
Cebidae
Pregnanediol
Leontopithecus
Cloprostenol
Animals, Laboratory
Hawks
Steatitis
Stomatognathic System
GB virus B
Databases, Protein
Protein Structure, Tertiary
Expression of the oxytocin receptor in relation to steroid receptors in the uterus of a primate model, the marmoset monkey. (1/878)
The dynamics of the receptors for oestrogen (ER), progesterone (PR) and oxytocin (OTR) in the marmoset uterus have been analysed throughout the entire cycle and early pregnancy. Uteri obtained during the early, mid/late and late proliferative phase, and the early, mid and late secretory phase and early pregnancy were examined by immunohistochemistry (OTR, ER, PR) and autoradiography (OTR). A massive upregulation of the ER in the cell nuclei of glandular epithelium and stromal cells during the mid proliferative phase was succeeded by a declining staining intensity and positively stained cell number in the secretory phase. PR immunoreactivity increased in the late proliferative phase and early secretory phase, mainly within the cell nuclei, and then declined in both intensity and cell number towards the mid to late secretory phase. Myometrium showed a similar staining pattern for the steroid receptors. OTR were expressed weakly in stroma throughout the entire cycle, increasing slightly in the secretory phase. Glandular epithelium showed positive staining only during the periovulatory period. Myometrial OTR expression was weak during the proliferative phase, increased towards the secretory phase, and was maximal in the late secretory phase. Myometrial tissue adjacent to endometrium was most strongly stained. A cyclic shift evidently occurred in the pattern of steroid receptors, perhaps reflecting the steroid environment or the luteinizing hormone increase associated with ovulation. (+info)Anatomical structure and surface epithelial distribution in the nasal cavity of the common cotton-eared marmoset (Callithrix jacchus). (2/878)
To validate use of the common cotton-eared marmoset (Callithrix jacchus) in inhalation toxicity studies, its nasal morphology was examined. The nasal turbinates each consisted of one maxilloturbinate and one ethmoturbinate: these were more planar in structure than the comparable structures of rodents or dogs. The nasal cavity epithelia comprised squamous epithelium (SE), nasal transitional epithelium (NTE), respiratory epithelium (RE) and olfactory epithelium (OE), listed in order of occurrence from anterior to posterior positions. NTE was distributed as a narrow band lying between SE and RE. OE was limited to the dorsal part of the cavity, which was structurally similar to that of the macaque or man. Overall, this study revealed structural the similarity of the whole nasal cavity in the marmoset to that of macaques or humans. Prediction of nasal cavity changes in man based on extrapolation from experimentally induced changes in the common marmoset therefore seems likely to be feasible, making it a useful animal model for inhalation studies. (+info)Role of cellular tumor necrosis factor receptor-associated factors in NF-kappaB activation and lymphocyte transformation by herpesvirus Saimiri STP. (3/878)
The STP oncoproteins of the herpesvirus saimiri (HVS) subgroup A strain 11 and subgroup C strain 488 are now found to be stably associated with tumor necrosis factor receptor-associated factor (TRAF) 1, 2, or 3. Mutational analyses identified residues of PXQXT/S in STP-A11 as critical for TRAF association. In addition, a somewhat divergent region of STP-C488 is critical for TRAF association. Mutational analysis also revealed that STP-C488 induced NF-kappaB activation that was correlated with its ability to associate with TRAFs. The HVS STP-C488 P10-->R mutant was deficient in human T-lymphocyte transformation to interleukin-2-independent growth but showed wild-type phenotype for marmoset T-lymphocyte transformation in vitro and in vivo. The STP-C488 P10-->R mutant was also defective in Rat-1 fibroblast transformation, and fibroblast cell transformation was blocked by a TRAF2 dominant-negative mutant. These data implicate TRAFs in STP-C488-mediated transformation of human lymphocytes and rodent fibroblasts. Other factors are implicated in immortalization of common marmoset T lymphocytes and may also be critical in the transformation of human lymphocytes and rodent fibroblasts. (+info)SR146131: a new potent, orally active, and selective nonpeptide cholecystokinin subtype 1 receptor agonist. II. In vivo pharmacological characterization. (4/878)
SR146131 is a potent and selective agonist at cholecystokinin subtype 1 (CCK1) receptors in vitro. The present study evaluates the activity of the compound in vivo. SR146131 completely inhibited gastric and gallbladder emptying in mice (ED50 of 66 and 2.7 micrograms/kg p.o., respectively). SR146131 dose dependently reduced food intake in fasted rats (from 0.1 mg/kg p.o.), in nonfasted rats in which food intake had been highly stimulated by the administration of neuropeptide Y (1-36) (from 0.3 mg/kg p.o.), in fasted gerbils (from 0.1 mg/kg p.o.), and in marmosets maintained on a restricted diet (from 3 mg/kg p.o.). SR146131 (10 mg/kg p.o.) also increased the number of Fos-positive cells in the hypothalamic paraventricular nucleus of rats. Locomotor activity of mice was reduced by orally administered SR146131 (from 0.3 mg/kg p.o.). When administered intrastriatally, SR146131 elicited contralateral turning behavior in mice. Furthermore, orally administered SR146131 (0.3-10 mg/kg), also reduced the levels of cerebellar cyclic GMP. Finally, SR146131 (0.1 microgram/kg to 1 mg/kg, p.o.) significantly and dose dependently antagonized fluphenazine-induced mouth movements in rats. The CCK1 antagonist SR27897B prevented all the effects of SR146131. Conversely, SR146131 was unable to elicit any agonist or antagonist effects in a model of CCK2 receptor stimulation in vivo. SR146131 is a very potent and selective nonpeptide CCK1 agonist in vivo. SR146131 is more potent than any other CCK1 agonists reported to date. Because pharmacodynamic studies suggest that SR146131 should have a high absolute bioavailability, it may be a promising drug for the treatment of eating and motor disorders in humans. (+info)The common marmoset as a target preclinical primate model for cytokine and gene therapy studies. (5/878)
Nonhuman primate models are useful to evaluate the safety and efficacy of new therapeutic modalities, including gene therapy, before the inititation of clinical trials in humans. With the aim of establishing safe and effective approaches to therapeutic gene transfer, we have been focusing on a small New World monkey, the common marmoset, as a target preclinical model. This animal is relatively inexpensive and easy to breed in limited space. First, we characterized marmoset blood and bone marrow progenitor cells (BMPCs) and showed that human cytokines were effective to maintain and stimulate in culture. We then examined their susceptibility to transduction by retroviral vectors. In a mixed culture system containing both marmoset stromal cells and retroviral producer cells, the transduction efficiency into BMPCs and peripheral blood progenitor cells (PBPCs) was 12% to 24%. A series of marmosets then underwent transplantation with autologous PBPCs transduced with a retroviral vector carrying the multidrug resistance 1 gene (MDR1) and were followed for the persistence of these cells in vivo. Proviral DNA was detectable by polymerase chain reaction (PCR) in peripheral blood granulocytes and lymphocytes in the recipients of gene transduced progenitors up to 400 days posttransplantation. To examine the function of the MDR1 gene in vivo, recipient maromsets were challenged with docetaxel, an MDR effluxed drug, yet the overall level of gene transfer attained in vivo (<1% in peripheral blood granulocytes) was not sufficient to prevent the neutropenia induced by docetaxel treatment. Using this model, we safely and easily performed a series of in vivo studies in our small animal center. Our results show that this small nonhuman primate, the common marmoset, is a useful model for the evaluation of gene transfer methods targeting hematopoietic stem cells. (+info)Design and evaluation of a ZP3 peptide vaccine in a homologous primate model. (6/878)
The concept of a safe, immunocontraceptive vaccine using the zona pellucida glycoprotein 3 (ZP3) as an immunogen has been marred by the appearance of ovarian dysfunction in several species. However, careful selection of epitopes on mouse ZP3 have demonstrated that it is possible to segregate contraceptive bone marrow-derived (B)-cell epitopes from the cytotoxic thymus-derived (T)-cell epitopes thought to be responsible for inducing ovarian disease. B-cell epitopes on marmoset ZP3 (mstZP3) were identified by epitope mapping studies. Using a panel of polyclonal antibodies against recombinant mstZP3, an immunodominant epitope mstZP3(301-320) was identified. A chimeric peptide was co-linearly synthesized incorporating this sequence with a promiscuous tetanus toxoid T-helper cell epitope. Using the common marmoset (Callithrix jacchus) as an animal model, we have compared the consequences of active immunization with homologous recombinant mstZP3 and mstZP3(301-320) chimeric peptide vaccine. Long-term infertility was achieved using mstZP3 but at the expense of ovarian function. In contrast, no disruption to ovarian function was observed following mstZP3(301-320) immunization. Antibodies to this peptide immunolocalized to the zona pellucida of both marmoset and human ovarian sections and inhibited human sperm-zona binding by approximately 60% in vitro. However, in-vivo studies indicated that targeting a single ZP3 epitope was insufficient to reliably and consistently achieve a contraceptive effect. (+info)High efficiency gene transfer to the central nervous system of rodents and primates using herpes virus vectors lacking functional ICP27 and ICP34.5. (7/878)
The safe and efficient use of herpes simplex virus (HSV)-based vectors to deliver genes of potentially therapeutic benefit to the central nervous system will require their effective disablement by the inactivation of viral genes required for lytic growth. Here we report that viruses lacking functional genes for ICP27 (which is required for growth in all cell types) and ICP34.5 (which is required for growth in nondividing cell types) can deliver a marker gene to both the rodent and primate CNS with high efficiency whilst producing relatively minimal damage and having no effect on sodium currents in dorsal root ganglion neurons. Such viruses paradoxically deliver genes at much higher efficiency than the less disabled single mutant lacking ICP34.5 alone and also, as expected, produce less damage in vivo. Moreover, unlike the single mutant lacking ICP27 the double mutant viruses cannot revert to wild-type by acquistion of complimenting gene sequences during growth of virus stocks in vitro on dividing cells expressing ICP27 since artificial expression of ICP34.5 in these cells is not required. Such ICP27-; ICP34.5- viruses thus offer a platform for the development of vectors which are sufficiently safe for ultimate use in human gene therapy. (+info)Normal development of refractive state and ocular component dimensions in the marmoset (Callithrix jacchus). (8/878)
Refractive state and ocular dimensions were studied longitudinally in nine normal marmosets. Animals were anaesthetised and examined (with some exceptions) at 4, 6, 7, 8, 10, 15, 24 and 39 weeks of age. Cycloplegic retinoscopy showed that hyperopia early in life rapidly diminished. Refraction corrected for the artefact of retinoscopy stabilised by 8 weeks of age, but at a slightly myopic value, rather than at emmetropia. The ocular components continued to change throughout the period studied. Corneal radius, measured by photokeratometry, increased slightly during development. Anterior segment depth and vitreous chamber depth (VCD), measured by A-scan ultrasonography, increased throughout development while lens thickness initially increased and then decreased. Data from the eyes of these normal animals were compared with that from the contralateral eyes of animals which received short periods of monocular deprivation early in life (Troilo, D., & Judge S.J. (1993). Ocular development and visual deprivation myopia in the common marmoset (Callithrix jacchus jacchus). Vision Research, 33, 1311-24); eyes which viewed through no lens or a plano lens (Graham, B. & Judge, S.J. (1999)). The effects of spectacle wear in infancy on eye growth and refractive error in the marmoset (Callithrix jacchus). Vision Research, 39, 189-206), and eyes of normal animals in another colony. There were no significant differences between the first two groups and the normal animals in our colony while age-matched animals from the other colony were slightly but significantly less myopic than our animals. (+info)Callithrix is a genus of New World monkeys, also known as marmosets. They are small, active primates found in the forests of South and Central America. The term "Callithrix" itself is derived from the Greek words "kallis" meaning beautiful and "thrix" meaning hair, referring to their thick, vibrantly colored fur.
Marmosets in the genus Callithrix are characterized by their slender bodies, long, bushy tails, and specialized dental structures that allow them to gouge tree bark to extract sap and exudates, which form a significant part of their diet. They also consume fruits, insects, and small vertebrates.
Some well-known species in this genus include the common marmoset (Callithrix jacchus), the white-headed marmoset (Callithrix geoffroyi), and the buffy-tufted-ear marmoset (Callithrix aurita). Marmosets are popular subjects of research due to their small size, short gestation period, and ease of breeding in captivity.
Callitrichinae is a subfamily of New World monkeys that includes marmosets and tamarins. These small primates are known for their claw-like nails (called "tegulae"), which they use for grooming and climbing, as well as their small size and social behavior. They are native to the forests of Central and South America. Some notable species in this subfamily include the common marmoset (Callithrix jacchus) and the golden lion tamarin (Leontopithecus rosalia).
There is no single medical definition for "Monkey Diseases." However, monkeys can carry and be infected with various diseases that are zoonotic, meaning they can be transmitted from animals to humans. Some examples include:
1. Simian Immunodeficiency Virus (SIV): A virus similar to Human Immunodeficiency Virus (HIV) that causes AIDS in monkeys. It is not typically harmful to monkeys but can cause AIDS in humans if transmitted, which is rare.
2. Herpes B Virus: Also known as Macacine herpesvirus 1 or Cercopithecine herpesvirus 1, it is a virus that commonly infects macaque monkeys. It can be transmitted to humans through direct contact with an infected monkey's saliva, eye fluid, or cerebrospinal fluid, causing a severe and potentially fatal illness called B encephalitis.
3. Tuberculosis (TB): Monkeys can contract and transmit tuberculosis to humans, although it is not common.
4. Simian Retrovirus (SRV): A virus that can infect both monkeys and great apes, causing immunodeficiency similar to HIV/AIDS in humans. It is not known to infect or cause disease in humans.
5. Various parasitic diseases: Monkeys can carry and transmit several parasites, including malaria-causing Plasmodium species, intestinal worms, and other parasites that can affect human health.
It's important to note that while monkeys can carry and transmit these diseases, the risk of transmission is generally low, and most cases occur in individuals who have close contact with monkeys, such as primatologists, zookeepers, or laboratory workers. Always follow safety guidelines when interacting with animals, including monkeys, to minimize the risk of disease transmission.
"Saguinus" is a genus of small, New World monkeys that are commonly known as tamarins. They are native to the forests of Central and South America. Tamarins have a slender body with long limbs, a specialized claw-like nail on their second digit of the foot, and a distinct coat coloration that varies between species. They primarily feed on fruits, insects, and exudates from trees. Tamarins are also known for their social structure, typically living in family groups consisting of a mated pair and their offspring.
"Paternal behavior" is not a term that has a specific medical definition. However, in general, it refers to the nurturing and protective behaviors exhibited by a male animal or human towards their offspring. In humans, paternal behavior can include providing financial support, emotional care, and protection for their children. It can also involve active involvement in child-rearing activities such as feeding, bathing, playing, teaching, and disciplining.
In some cases, "paternal behavior" may be used to describe a syndrome or set of behaviors exhibited by individuals who have a particular genetic mutation associated with increased paternal caregiving. However, this is not a widely recognized medical term or condition.
It's worth noting that the study of paternal behavior and its impact on child development has gained increasing attention in recent years, as researchers seek to better understand the complex interplay between genetic, hormonal, and environmental factors that shape parenting behaviors and outcomes for children.
Cebidae is a family of primates that includes monkeys and capuchins found in the tropical rainforests and woodlands of Central and South America. This family is divided into two subfamilies: Cebinae (capuchin monkeys) and Saimiriinae (squirrel monkeys). These animals are known for their adaptability, complex social structures, and diverse behaviors. They have a varied diet that includes fruits, nuts, seeds, insects, and small vertebrates. Some notable members of this family include the white-faced capuchin, the black-capped squirrel monkey, and the golden lion tamarin.
Pregnanediol is a steroid hormone that is produced as a metabolite of progesterone. It is primarily used as a biomarker to measure the exposure to progesterone, particularly in cases where progesterone levels need to be monitored, such as during pregnancy or in certain medical conditions. Pregnanediol can be measured in urine, blood, or other bodily fluids and is often used in clinical and research settings to assess hormonal status. It is important to note that pregnanediol itself does not have any known physiological effects on the body, but rather serves as an indicator of progesterone levels.
"Leontopithecus" is not a medical term, but a taxonomic genus name in the field of zoology. It refers to a group of small New World monkeys known as lion tamarins, which are native to the Atlantic coastal forests of Brazil. These primates are characterized by their thick manes that resemble those of lions, hence their common name.
The medical community may be interested in Leontopithecus species due to their potential use in biomedical research or conservation efforts. However, it is not a term commonly used in medical practice or literature.
Cloprostenol is a synthetic prostaglandin analog used primarily in veterinary medicine for the treatment and prevention of various conditions. The main therapeutic uses of Cloprostenol include:
1. Induction of parturition (labor) in cows, helping to synchronize calving in managed herds.
2. Termination of pregnancy in cattle, especially in cases where the fetus is nonviable or the pregnancy poses a risk to the animal's health.
3. Treatment of uterine and oviductal disorders, such as pyometra (infection of the uterus) and salpingitis (inflammation of the oviduct), in cattle and pigs.
4. Prevention of postpartum disorders, like endometritis (inflammation of the lining of the uterus) and mastitis (inflammation of the mammary glands), by promoting uterine involution and improving overall reproductive performance in cattle.
5. Control of estrus (heat) in cattle, as an aid in estrous synchronization programs for artificial insemination.
Cloprostenol is available in various formulations, such as intramuscular or subcutaneous injectable solutions, and is typically administered by a veterinarian or trained personnel. It is important to note that the use of Cloprostenol and other prostaglandin analogs should be carried out under the guidance and supervision of a veterinary professional, as improper usage can lead to adverse effects or complications.
'Laboratory animals' are defined as non-human creatures that are used in scientific research and experiments to study various biological phenomena, develop new medical treatments and therapies, test the safety and efficacy of drugs, medical devices, and other products. These animals are kept under controlled conditions in laboratory settings and are typically purpose-bred for research purposes.
The use of laboratory animals is subject to strict regulations and guidelines to ensure their humane treatment and welfare. The most commonly used species include mice, rats, rabbits, guinea pigs, hamsters, dogs, cats, non-human primates, and fish. Other less common species may also be used depending on the specific research question being studied.
The primary goal of using laboratory animals in research is to advance our understanding of basic biological processes and develop new medical treatments that can improve human and animal health. However, it is important to note that the use of animals in research remains a controversial topic due to ethical concerns regarding their welfare and potential for suffering.
I'm sorry for any confusion, but "Hawks" is not a commonly used medical term. It is most frequently associated with the bird of prey or a sports team name. If you have encountered this term in a medical context and are unsure of its meaning, I would recommend checking the source again or consulting with a healthcare professional for clarification.
Steatitis is a medical term that refers to the inflammation of fatty tissue, also known as nonalcoholic fatty liver disease (NAFLD) when it occurs in the liver. It is often caused by the accumulation of large amounts of fat within cells, leading to oxidative stress and an immune response.
Steatitis can occur in various parts of the body, including the abdominal cavity, bone marrow, and other organs. However, when it occurs in the liver, it is often associated with obesity, metabolic syndrome, and diabetes. In severe cases, steatitis in the liver can lead to scarring, cirrhosis, and even liver failure.
Symptoms of steatitis may include fatigue, abdominal pain or discomfort, loss of appetite, weight loss, and nausea. Diagnosis typically involves a combination of physical exam, medical history, imaging studies, and laboratory tests. Treatment options may include lifestyle changes such as diet and exercise, medications to manage underlying conditions, and in some cases, surgery.
The stomatognathic system is a term used in medicine and dentistry to refer to the coordinated functions of the mouth, jaw, and related structures. It includes the teeth, gums, tongue, palate, lips, cheeks, salivary glands, as well as the muscles of mastication (chewing), swallowing, and speech. The stomatognathic system also involves the temporomandibular joint (TMJ) and associated structures that allow for movement of the jaw. This complex system works together to enable functions such as eating, speaking, and breathing. Dysfunction in the stomatognathic system can lead to various oral health issues, including temporomandibular disorders, occlusal problems, and orofacial pain.
GB virus B (GBV-B) is not a widely accepted or used term in the medical community. It was initially identified as a possible new virus in the 1960s, during an investigation into hepatitis outbreaks among laboratory workers handling chimpanzee serum and feces. However, further research could not confirm its existence as a separate virus.
The name "GB virus B" comes from the initials of the person (G. Barker) who provided the original serum sample where the virus was first detected, and "B" to differentiate it from another related virus called GB virus A (GBV-A).
Currently, GBV-B is not considered a distinct human pathogen or a significant cause of any known diseases. It is not included in the list of human viruses by the International Committee on Taxonomy of Viruses (ICTV) and is not recognized as a medical condition by major health organizations such as the World Health Organization (WHO) or the Centers for Disease Control and Prevention (CDC).
A protein database is a type of biological database that contains information about proteins and their structures, functions, sequences, and interactions with other molecules. These databases can include experimentally determined data, such as protein sequences derived from DNA sequencing or mass spectrometry, as well as predicted data based on computational methods.
Some examples of protein databases include:
1. UniProtKB: a comprehensive protein database that provides information about protein sequences, functions, and structures, as well as literature references and links to other resources.
2. PDB (Protein Data Bank): a database of three-dimensional protein structures determined by experimental methods such as X-ray crystallography and nuclear magnetic resonance (NMR) spectroscopy.
3. BLAST (Basic Local Alignment Search Tool): a web-based tool that allows users to compare a query protein sequence against a protein database to identify similar sequences and potential functional relationships.
4. InterPro: a database of protein families, domains, and functional sites that provides information about protein function based on sequence analysis and other data.
5. STRING (Search Tool for the Retrieval of Interacting Genes/Proteins): a database of known and predicted protein-protein interactions, including physical and functional associations.
Protein databases are essential tools in proteomics research, enabling researchers to study protein function, evolution, and interaction networks on a large scale.
Tertiary protein structure refers to the three-dimensional arrangement of all the elements (polypeptide chains) of a single protein molecule. It is the highest level of structural organization and results from interactions between various side chains (R groups) of the amino acids that make up the protein. These interactions, which include hydrogen bonds, ionic bonds, van der Waals forces, and disulfide bridges, give the protein its unique shape and stability, which in turn determines its function. The tertiary structure of a protein can be stabilized by various factors such as temperature, pH, and the presence of certain ions. Any changes in these factors can lead to denaturation, where the protein loses its tertiary structure and thus its function.