Receptor, Melanocortin, Type 3
Arthritis, Gouty
Receptors, Melanocortin
Receptor, Melanocortin, Type 4
alpha-MSH
Receptor, Melanocortin, Type 1
Receptor, Melanocortin, Type 2
Receptors, Corticotropin
Melanocyte-Stimulating Hormones
Agouti-Related Protein
Agouti Signaling Protein
gamma-MSH
beta-MSH
Sebaceous Gland Diseases
Hypothalamus
Arcuate Nucleus
Peptides, Cyclic
Adrenocorticotropic Hormone
Leptin
Neuropeptide Y
Cosyntropin
Haploinsufficiency of steroidogenic factor-1 in mice disrupts adrenal development leading to an impaired stress response. (1/51)
Adrenal steroids are essential for homeostasis and survival during severe physiological stress. Analysis of a patient heterozygous for the steroidogenic factor-1 (SF-1) gene suggested that reduced expression of this nuclear receptor leads to adrenal failure. We therefore examined SF-1 heterozygous (+/-) mice as a potential model for delineating mechanisms underlying this disease. Here we show that SF-1 +/- mice exhibit adrenal insufficiency resulting from profound defects in adrenal development and organization. However, compensatory mechanisms, such as cellular hypertrophy and increased expression of the rate-limiting steroidogenic protein StAR, help to maintain adrenal function at near normal capacity under basal conditions. In contrast, adrenal deficits in SF-1 heterozygotes are revealed under stressful conditions, demonstrating that normal gene dosage of SF-1 is required for mounting an adequate stress response. Our findings predict that natural variations leading to reduced SF-1 function may underlie some forms of subclinical adrenal insufficiency, which become life threatening during traumatic stress. (+info)Failed export of the adrenocorticotrophin receptor from the endoplasmic reticulum in non-adrenal cells: evidence in support of a requirement for a specific adrenal accessory factor. (2/51)
Difficulty in expressing the adrenocorticotrophin (ACTH) receptor (melanocortin 2 receptor; MC2R) after transfection of various MC2R expression vectors has been experienced by many researchers. Reproducible evidence for expression has been obtained only in the Y6/OS3 corticoadrenal cell lines or in cells expressing endogenous melanocortin receptors. In order to determine the cause of this failure of expression we have undertaken the following studies. An MC2R expression plasmid was constructed in which the green fluorescent protein (GFP) coding region had been added to the C-terminus of the mature protein. Transfection of this plasmid into Y6 cells with a cAMP-responsive reporter plasmid demonstrated normal function of this receptor. Imaging of CHO cells expressing MC2R-GFP revealed perinuclear expression, although a cholecystokinin receptor (CCKR)-GFP construct was efficiently expressed at the cell surface. Y6 cells, in contrast, showed cell surface fluorescence after transfection with MC2R-GFP. Several other cell types showed a similar pattern of GFP distribution characteristic of retention in the endoplasmic reticulum. Counterstaining with an anti-KDEL antibody confirmed this location. Co-expression of the MC2R and the CCKR-GFP did not impair CCKR trafficking to the cell surface, implying a receptor-specific impairment to trafficking in the CHO cell which was absent in the Y6 cell. (+info)Inhibition of tumor necrosis factor-alpha stimulated NFkappaB/p65 in human keratinocytes by alpha-melanocyte stimulating hormone and adrenocorticotropic hormone peptides. (3/51)
Alpha-melanocyte stimulating hormone (alpha-MSH) has pigmentary, anti-inflammatory, antipyretic, and general immunomodulatory roles. It can oppose several cytokines including tumor necrosis factor-alpha in a number of tissues, including skin. We have previously shown that alpha-MSH can inhibit tumor necrosis factor-alpha stimulated intercellular adhesion molecule 1 upregulation and nuclear factor kappaB (NFkappaB) transcription factor activation in melanocyte and melanoma cells. It is thought, however, that this MSH biology may also extend to other cells of the skin and in this study we extend our work to keratinocytes. We have investigated in detail the ability of three alpha-MSH peptides to inhibit tumor necrosis factor alpha stimulated NFkappaB activation in nonpigmentary HaCaT keratinocytes (alpha-MSH, L-Lys-L-Pro-L-Val, and L-Lys-L-Pro-D-Val) and two adrenocorticotropic hormone (ACTH) peptides (1-17 and 1-39), reported to be present in skin tissue. NFkappaB/p65 activation was analyzed by electrophoretic mobility shift assay and immunofluorescent microscopy. alpha-MSH, L-Lys-L-Pro-L-Val, and L-Lys-L-Pro-D-Val all significantly inhibited tumor necrosis factor alpha stimulated NFkappaB activation, whereas ACTH 1-17 and 1-39 did not, in the HaCaT keratinocytes. MSH peptides and ACTH 1-39 were effective, however, at inhibiting NFkappaB activation in normal human keratinocytes. Immunolabeling of inhibitor kappaBalpha of NFkappaB (IkappaBalpha) revealed an abnormal localization to the nucleus of HaCaT cells, which was unaffected by MSH/ACTH peptides. In contrast, normal human keratinocytes showed a normal IkappaBalpha distribution that responded to MSH/ACTH with nuclear translocation. Our data support previous work on the role of MSH/ACTH peptides as immunomodulatory/anti-inflammatory regulators, and extend this work to keratinocytes identifying a novel IkappaBalpha mechanism and extends findings to ACTH peptides, identifying an abnormal IkappaBalpha mechanism in the immortal HaCaT versus normal keratinocyte. (+info)Agouti expression in human adipose tissue: functional consequences and increased expression in type 2 diabetes. (4/51)
It is well recognized that the agouti/melanocortin system is an important regulator of body weight homeostasis. Given that agouti is expressed in human adipose tissue and that the ectopic expression of agouti in adipose tissue results in moderately obese mice, the link between agouti expression in human adipose tissue and obesity/type 2 diabetes was investigated. Although there was no apparent relationship between agouti mRNA levels and BMI, agouti mRNA levels were significantly elevated in subjects with type 2 diabetes. The regulation of agouti in cultured human adipocytes revealed that insulin did not regulate agouti mRNA, whereas dexamethasone treatment potently increased the levels of agouti mRNA. Experiments with cultured human preadipocytes and with cells obtained from transgenic mice that overexpress agouti demonstrated that melanocortin receptor (MCR) signaling in adipose tissue can regulate both preadipocyte proliferation and differentiation. Taken together, these results reveal that agouti can regulate adipogenesis at several levels and suggest that there are functional consequences of elevated agouti levels in human adipose tissue. The influence of MCR signaling on adipogenesis combined with the well-established role of MCR signaling in the hypothalamus suggest that adipogenesis is coordinately regulated with food intake and energy expenditure. (+info)ACTH stimulates insulin secretion from MIN6 cells and primary mouse and human islets of Langerhans. (5/51)
It has previously been suggested that ACTH and ACTH-related peptides may act as paracrine modulators of insulin secretion in the islets of Langerhans. We have, therefore, examined the expression and function of the ACTH receptor (the melanocortin 2 receptor, MC2-R) in human and mouse primary islet tIssue and in the MIN6 mouse insulinoma cell line. Mouse MC2-R mRNA was detected in both MIN6 cells and mouse islet tIssue by PCR amplification of cDNA. In perifusion experiments with MIN6 pseudo-islets, a small, transient increase in insulin secretion was obtained when ACTH(1-24) (1 nM) was added to medium containing 2 mM glucose (control) but not when the medium glucose content was increased to 8 mM. Further investigations were performed using static incubations of MIN6 cell monolayers; ACTH(1-24) (1 pM-10 nM) provoked a concentration-dependent increase in insulin secretion from MIN6 monolayer cells that achieved statistical significance at concentrations of 1 and 10 nM (150 +/- 13.6% basal secretion; 187 +/- 14.9% basal secretion, P<0.01). Similar responses were obtained with ACTH(1-39). The phosphodiesterase inhibitor IBMX (100 microM) potentiated the responses to sub-maximal doses of ACTH(1-24). Two inhibitors of the protein kinase A (PKA) signaling pathway, Rp-cAMPS (500 microM) and H-89 (10 microM), abolished the insulin secretory response to ACTH(1-24) (0.5-10 nM). Treatment with 1 nM ACTH(1-24) caused a small, statistically significant increase in intracellular cAMP levels. Secretory responses of MIN6 cells to ACTH(1-24) were also influenced by changes in extracellular Ca2+ levels. Incubation in Ca2+-free buffer supplemented with 0.1 mM EGTA blocked the MIN6 cells' secretory response to 1 and 10 nM ACTH(1-24). Similar results were obtained when a Ca2+ channel blocker (nitrendipine, 10 microM) was added to the Ca2+-containing buffer. ACTH(1-24) also evoked an insulin secretory response from primary tIssues. The addition of ACTH(1-24) (0.5 nM) to perifusions of mouse islets induced a transient increase in insulin secretion at 8 mM glucose. Perifused human primary islets also showed a secretory response to ACTH(1-24) at basal glucose concentration (2 mM) with a rapid initial spike in insulin secretion followed by a decline to basal levels. Overall the results demonstrate that the MC2-R is expressed in beta-cells and suggest that activation of the receptor by ACTH initiates insulin secretion through the activation of PKA in association with Ca2+ influx into beta-cells. (+info)A peroxisome proliferator-response element in the murine mc2-r promoter regulates its transcriptional activation during differentiation of 3T3-L1 adipocytes. (6/51)
Adrenocorticotropic hormone can stimulate lipolysis and suppress leptin expression in murine adipocytes. These effects are mediated via the melanocortin 2 receptor (MC2-R), which is expressed when 3T3-L1 cells are induced to undergo adipogenesis. In this study, we have characterized the mc2-r promoter in the murine adipocyte, one of the few extra-adrenal sites of expression and a cell type that lacks steroidogenic factor 1 (SF-1), a transcription factor that is required for mc2-r expression in adrenal cells. Transcriptional regulation of the mc2-r in the absence of SF-1 was investigated by 5' deletion analysis of the murine mc2-r promoter in both undifferentiated and differentiated 3T3-L1 cells. The results revealed the presence of a 59-base pair regulatory region within the promoter containing an adipocyte-specific enhancer. The ability of this region to confer enhanced activity in the adipocyte was mapped to a peroxisome proliferator-response element (PPRE)-like sequence that bound to peroxisome proliferator-activated receptor gamma (PPARgamma) and its heterodimeric partner retinoid X receptor alpha (RXRalpha) in adipocyte nuclear extracts. Co-transfection of PPARgamma2/RXRalpha with the pMC2-R(-112/+105)GL3 reporter resulted in transcriptional activation in preadipocytes, and this response required an intact PPRE. Mutation of the PPRE to prevent PPARgamma/RXRalpha binding resulted in a complete abrogation of the pMC2-R(-112/+105)GL3 reporter activity in day 3 differentiated 3T3-L1 cells, demonstrating a key role played by this site in regulating MC2-R expression in the murine adipocyte. These data highlight a novel mechanism for mc2-r transcription, which may have significance in both adrenal and extra-adrenal sites of expression. (+info)An E-box-containing region is involved in the tissue-specific expression of the human MC2R gene. (7/51)
Expression of the melanocortin receptor (MC2R) gene is limited to adrenocortical cells and the aim of this study was to determine the factors responsible for this tissue specificity. We used different fragments of the human (h) MC2R gene promoter, inserted in a vector upstream of the luciferase reporter gene, to transiently transfect either bovine adrenocortical (BAC) cells or granulosa cells from bovine ovaries (B-Gran). Similar promoter activities were obtained in both cell types using constructs containing fragments up to 1017 bp of the hMC2R gene promoter. On the contrary, a 2-fold decrease was obtained after transfection of the B-Gran cells with vectors containing 1069 bp and more of the promoter. Results obtained here using BAC cells confirmed our previous data on human cells showing that steroidogenic factor 1 is the major transactivating factor involved in the basal expression of the hMC2R gene in adrenal cells. However, we showed that this factor did not permit, by itself, the expression of the hMC2R gene in B-Gran cells despite its expression in these cells. This study demonstrated for the first time that an E-box (located at -1020 bp) is involved in the repression of hMC2R gene expression in granulosa cells through interactions with several factors, such as activator protein 4, as suggested by electrophoretic mobility shift assay analyses. (+info)Differential actions of metyrapone on the fetal pituitary-adrenal axis in the sheep fetus in late gestation. (8/51)
It is not clear if an increase in intra-adrenal cortisol is required to mediate the actions of adrenocorticotropic hormone (ACTH) on adrenal growth and steroidogenesis during the prepartum stimulation of the fetal pituitary-adrenal axis. We infused metyrapone, a competitive inhibitor of cortisol biosynthesis, into fetal sheep between 125 and 140 days of gestation (term = 147 +/- 3 days) and measured fetal plasma cortisol, 11-desoxycortisol, and ACTH; pituitary pro-opiomelanocortin mRNA and adrenal expression of ACTH receptor (melanocortin type 2 receptor), steroidogenic acute regulatory protein (StAR), 11beta-hydroxysteroid dehydrogenase type 2 (11betaHSD2), cytochrome P450 cholesterol side-chain cleavage (CYP11A1), cytochrome P450 17-hydroxylase (CYP17), 3beta-hydroxysteroid dehydrogenase, and cytochrome P450 21-hydroxylase mRNA; and StAR protein in the fetal adrenal gland. Plasma ACTH and 11-desoxycortisol concentrations were higher (P < 0.05), whereas plasma cortisol concentrations were not significantly different in metyrapone- compared with vehicle-infused fetuses. The ratio of plasma cortisol to ACTH concentrations was higher (P < 0.0001) between 136 and 140 days than between 120 and 135 days of gestation in both metyrapone- and vehicle-infused fetuses. The combined adrenal weight and adrenocortical thickness were greater (P < 0.001), and cell density was lower (P < 0.01), in the zona fasciculata of adrenals from the metyrapone-infused group. Adrenal StAR mRNA expression was lower (P < 0.05), whereas the levels of mature StAR protein (30 kDa) were higher (P < 0.05), in the metyrapone-infused fetuses. In addition, adrenal mRNA expression of 11betaHSD2, CYP11A1, and CYP17 were higher (P < 0.05) in the metyrapone-infused fetuses. Thus, metyrapone administration may represent a unique model that allows the investigation of dissociation of the relative actions of ACTH and cortisol on fetal adrenal steroidogenesis and growth during late gestation. (+info)A melanocortin receptor (MCR) is a type of G protein-coupled receptor that binds melanocortin peptides. The melanocortin system plays crucial roles in various biological processes such as pigmentation, energy homeostasis, sexual function, and inflammation.
The melanocortin receptor type 3 (MC3R) is one of the five subtypes of MCRs (MC1R to MC5R). It is widely expressed in the central nervous system, including the hypothalamus, and is involved in the regulation of energy balance, feeding behavior, and body weight.
The endogenous ligands for MC3R include α-melanocyte stimulating hormone (α-MSH) and adrenocorticotropic hormone (ACTH), which are derived from the precursor protein proopiomelanocortin (POMC). Activation of MC3R by these ligands leads to a decrease in food intake and an increase in energy expenditure, contributing to weight loss. However, the exact mechanisms through which MC3R modulates these physiological functions are not yet fully understood.
Gouty arthritis is a type of inflammatory arthritis that occurs due to the buildup of uric acid crystals in the joints. Uric acid is a waste product that is formed when the body breaks down purines, which are substances found naturally in the body and in certain foods such as organ meats, anchovies, sardines, and beer.
In people with gouty arthritis, uric acid levels in the blood become elevated, leading to the formation of sharp, needle-like crystals that can accumulate in the joints, causing pain, inflammation, and swelling. The symptoms of gouty arthritis typically occur suddenly and may include:
* Intense pain in the affected joint, often occurring at night
* Redness, warmth, and swelling in the affected area
* Stiffness and limited mobility in the affected joint
The most commonly affected joint is the big toe, but gouty arthritis can also occur in other joints such as the ankles, knees, wrists, and fingers. Over time, repeated episodes of gouty arthritis can lead to joint damage and chronic pain. Treatment typically involves medications to reduce inflammation and manage pain, as well as lifestyle changes to lower uric acid levels in the body.
Melanocortin receptors (MCRs) are a group of G protein-coupled receptors that bind melanocortin peptides, which include α-, β-, and γ-melanocyte stimulating hormones (MSH) and adrenocorticotropic hormone (ACTH). These receptors are involved in a variety of physiological processes, including pigmentation, energy homeostasis, sexual function, and inflammation. There are five subtypes of melanocortin receptors (MCR1-5) that are expressed in different tissues and have distinct functions.
MCR1 is primarily expressed in melanocytes and plays a crucial role in skin and hair pigmentation. Activation of MCR1 by α-MSH leads to the production and distribution of eumelanin, which results in darker skin and hair.
MCR2 is widely expressed in the central nervous system (CNS) and peripheral tissues, including the adrenal gland, testis, and ovary. It is involved in various functions such as sexual function, feeding behavior, and energy homeostasis.
MCR3 is primarily expressed in the adrenal gland and plays a critical role in the regulation of steroid hormone production and release. Activation of MCR3 by ACTH leads to the synthesis and secretion of cortisol and other steroid hormones.
MCR4 is widely expressed in the CNS, peripheral tissues, and immune cells. It is involved in various functions such as energy homeostasis, feeding behavior, sexual function, and inflammation.
MCR5 is primarily expressed in the testis and plays a role in spermatogenesis and fertility.
Overall, melanocortin receptors are important regulators of various physiological processes, and dysregulation of these receptors has been implicated in several diseases, including obesity, metabolic disorders, and skin disorders.
A melanocortin receptor (MCR) is a type of G protein-coupled receptor that binds melanocortin peptides. The melanocortin system plays crucial roles in various biological processes such as pigmentation, energy homeostasis, sexual function, and inflammation.
The melanocortin receptor 4 (MC4R) is one of the five subtypes of MCRs, which is widely expressed in the central nervous system, including the hypothalamus, and some peripheral tissues. MC4R is a key component in the regulation of energy balance, appetite, and body weight. Activation of MC4R by melanocortin peptides, such as α-melanocyte stimulating hormone (α-MSH), leads to decreased food intake and increased energy expenditure, while antagonism or deficiency of MC4R results in obesity.
In summary, the medical definition of 'Receptor, Melanocortin, Type 4' is a G protein-coupled receptor that binds melanocortin peptides and plays a critical role in regulating energy balance, appetite, and body weight.
Alpha-MSH (α-MSH) stands for alpha-melanocyte stimulating hormone. It is a peptide hormone that is produced in the pituitary gland and other tissues in the body. Alpha-MSH plays a role in various physiological processes, including:
1. Melanin production: Alpha-MSH stimulates melanin production in the skin, which leads to skin tanning.
2. Appetite regulation: Alpha-MSH acts as a appetite suppressant by signaling to the brain that the stomach is full.
3. Inflammation and immune response: Alpha-MSH has anti-inflammatory effects and helps regulate the immune response.
4. Energy balance and metabolism: Alpha-MSH helps regulate energy balance and metabolism by signaling to the brain to increase or decrease food intake and energy expenditure.
Alpha-MSH exerts its effects by binding to melanocortin receptors, specifically MC1R, MC3R, MC4R, and MC5R. Dysregulation of alpha-MSH signaling has been implicated in various medical conditions, including obesity, anorexia nervosa, and certain skin disorders.
A melanocortin receptor (MCR) is a type of G protein-coupled receptor that binds melanocortin peptides. The melanocortin-1 receptor (MC1R) is one of five known subtypes of MCRs (MC1R-MC5R).
The MC1R is primarily expressed in melanocytes, which are pigment-producing cells located in the skin, hair follicles, and eyes. This receptor plays a crucial role in determining the type of melanin that is produced in response to environmental stimuli such as UV radiation.
Activation of the MC1R by its endogenous ligands, including α-melanocyte-stimulating hormone (α-MSH) and adrenocorticotropic hormone (ACTH), leads to the activation of adenylate cyclase and an increase in intracellular cAMP levels. This results in the activation of protein kinase A and the phosphorylation of key transcription factors, which ultimately promote the expression of genes involved in melanin synthesis.
Mutations in the MC1R gene have been associated with various pigmentation disorders, including red hair color, fair skin, and an increased risk of developing skin cancer. Additionally, polymorphisms in the MC1R gene have been linked to an increased risk of developing other diseases such as obesity and type 2 diabetes.
A melanocortin type 2 receptor (MC2R) is a G protein-coupled receptor that binds melanocortin peptides such as adrenocorticotropic hormone (ACTH). It is primarily expressed in the adrenal gland, specifically in the zona fasciculata of the cortex. Upon activation by ACTH, MC2R stimulates the production and release of steroid hormones, particularly cortisol, through the cAMP signaling pathway. Dysfunction in this receptor can lead to various endocrine disorders such as congenital adrenal hyperplasia and Cushing's disease.
Corticotropin receptors are a type of cell surface receptor that bind to the hormone corticotropin (also known as adrenocorticotropic hormone or ACTH). These receptors are found in various tissues throughout the body, including the adrenal glands.
There are two main types of corticotropin receptors, known as melanocortin receptor 1 (MC1R) and melanocortin receptor 2 (MC2R). MC2R is the primary receptor for corticotropin in the adrenal glands. When corticotropin binds to this receptor, it stimulates the production and release of steroid hormones, such as cortisol, which help regulate metabolism, immune response, and stress response.
Abnormalities in corticotropin receptors have been implicated in several medical conditions, including certain endocrine disorders and skin pigmentation disorders.
Melanocyte-stimulating hormones (MSH) are a group of peptide hormones that originate from the precursor protein proopiomelanocortin (POMC). They play crucial roles in various physiological processes, including pigmentation, energy balance, and appetite regulation.
There are several types of MSH, but the most well-known ones include α-MSH, β-MSH, and γ-MSH. These hormones bind to melanocortin receptors (MCRs), which are found in various tissues throughout the body. The binding of MSH to MCRs triggers a series of intracellular signaling events that ultimately lead to changes in cell behavior.
In the context of skin physiology, α-MSH and β-MSH bind to melanocortin 1 receptor (MC1R) on melanocytes, which are the cells responsible for producing pigment (melanin). This binding stimulates the production and release of eumelanin, a type of melanin that is brown or black in color. As a result, increased levels of MSH can lead to darkening of the skin, also known as hyperpigmentation.
Apart from their role in pigmentation, MSH hormones have been implicated in several other physiological processes. For instance, α-MSH has been shown to suppress appetite and promote weight loss by binding to melanocortin 4 receptor (MC4R) in the hypothalamus, a region of the brain that regulates energy balance. Additionally, MSH hormones have been implicated in inflammation, immune response, and sexual function.
Overall, melanocyte-stimulating hormones are a diverse group of peptide hormones that play important roles in various physiological processes, including pigmentation, energy balance, and appetite regulation.
Agouti-related protein (AGRP) is a neuropeptide that functions as an endogenous antagonist of melanocortin receptors, specifically MC3R and MC4R. It is expressed in the hypothalamus and plays a crucial role in regulating energy balance, body weight, and glucose homeostasis. AGRP increases food intake and decreases energy expenditure by inhibiting melanocortin signaling in the hypothalamus. Dysregulation of AGRP has been implicated in various metabolic disorders, including obesity and type 2 diabetes.
Agouti signaling protein (ASP) is a protein that in humans is encoded by the ASIP gene. It is a paracrine signaling molecule that regulates melanin synthesis in the hair follicle and plays a critical role in determining coat color in mammals. ASP binds to and antagonizes the melanocortin-1 receptor (MC1R), which is a G protein-coupled receptor found on the surface of melanocytes, the cells that produce melanin.
When ASP binds to MC1R, it inhibits the activation of adenylyl cyclase and reduces the intracellular levels of cAMP, which in turn leads to a decrease in eumelanin (black or brown) production and an increase in pheomelanin (yellow or red) production. This switch in melanin synthesis results in a banded coat pattern, as seen in the agouti mouse and some other mammals.
In addition to its role in coat color determination, ASP has been implicated in various physiological processes, including energy homeostasis, appetite regulation, and inflammation. Dysregulation of ASP function has been associated with obesity, metabolic disorders, and certain types of cancer.
Gamma-MSH (Gamma-Melanocyte Stimulating Hormone) is a type of melanocyte stimulating hormone that is produced in the human body. It is a tripeptide, consisting of four amino acids (His-Phe-Arg-Trp), and is a cleavage product of the proopiomelanocortin (POMC) peptide.
Gamma-MSH plays a role in regulating pigmentation in the skin by stimulating melanin production in melanocytes, which are specialized cells found in the skin. It also has been shown to have potential effects on appetite regulation and energy balance, as well as anti-inflammatory and neuroprotective properties. However, its precise physiological roles and therapeutic potentials remain an area of ongoing research.
I'm sorry for any confusion, but "hair color" is not a term that has a medical definition in the same way that a term like "myocardial infarction" (heart attack) does. Hair color can be described in various ways, such as being a natural hair color (like blonde, brunette, red, or black) or describing a change in hair color due to factors like aging (gray or white hairs) or hair dye usage.
However, it's worth noting that changes in hair color can sometimes be associated with certain medical conditions. For example, premature graying of the hair before the age of 30 can be a feature of certain genetic disorders or vitamin B12 deficiency. Similarly, some skin conditions like alopecia areata or vitiligo can cause patchy changes in hair color. But these associations don't provide a medical definition for 'hair color'.
Beta-MSH (beta-melanocyte-stimulating hormone) is a neuropeptide that is a cleavage product of the proopiomelanocortin (POMC) protein. It plays a role in regulating melanin production in the skin and has been found to have appetite suppressant effects, making it a target for obesity research. Beta-MSH acts as an agonist at melanocortin receptors MC3R and MC4R, which are involved in energy balance and feeding behavior.
Sebaceous gland diseases refer to conditions that affect the sebaceous glands, which are small glands in the skin that produce an oily substance called sebum. Sebum helps keep the skin and hair moisturized. Sebaceous gland diseases can cause a variety of symptoms, including skin inflammation, redness, pain, and the formation of bumps or cysts.
Some common types of sebaceous gland diseases include:
1. Acne: A common skin condition that occurs when the hair follicles become plugged with oil and dead skin cells, leading to whiteheads, blackheads, or pimples.
2. Seborrheic dermatitis: A skin condition that causes red, itchy, and flaky skin, often on the scalp, face, or chest.
3. Rosacea: A chronic skin condition that causes redness, pimples, and visible blood vessels on the face.
4. Sebaceous hyperplasia: A benign growth of the sebaceous glands that appears as a small, yellowish bump on the skin.
5. Sebaceous adenitis: A rare inflammatory disease that affects the sebaceous glands, causing hair loss and scaly skin.
6. Sebaceous carcinoma: A rare and aggressive form of skin cancer that develops in the sebaceous glands.
Treatment for sebaceous gland diseases depends on the specific condition and its severity. Treatments may include topical or oral medications, light therapy, or surgical removal of affected tissue. It is important to consult a healthcare provider for an accurate diagnosis and treatment plan.
The medical definition of "eating" refers to the process of consuming and ingesting food or nutrients into the body. This process typically involves several steps, including:
1. Food preparation: This may involve cleaning, chopping, cooking, or combining ingredients to make them ready for consumption.
2. Ingestion: The act of taking food or nutrients into the mouth and swallowing it.
3. Digestion: Once food is ingested, it travels down the esophagus and enters the stomach, where it is broken down by enzymes and acids to facilitate absorption of nutrients.
4. Absorption: Nutrients are absorbed through the walls of the small intestine and transported to cells throughout the body for use as energy or building blocks for growth and repair.
5. Elimination: Undigested food and waste products are eliminated from the body through the large intestine (colon) and rectum.
Eating is an essential function that provides the body with the nutrients it needs to maintain health, grow, and repair itself. Disorders of eating, such as anorexia nervosa or bulimia nervosa, can have serious consequences for physical and mental health.
The hypothalamus is a small, vital region of the brain that lies just below the thalamus and forms part of the limbic system. It plays a crucial role in many important functions including:
1. Regulation of body temperature, hunger, thirst, fatigue, sleep, and circadian rhythms.
2. Production and regulation of hormones through its connection with the pituitary gland (the hypophysis). It controls the release of various hormones by producing releasing and inhibiting factors that regulate the anterior pituitary's function.
3. Emotional responses, behavior, and memory formation through its connections with the limbic system structures like the amygdala and hippocampus.
4. Autonomic nervous system regulation, which controls involuntary physiological functions such as heart rate, blood pressure, and digestion.
5. Regulation of the immune system by interacting with the autonomic nervous system.
Damage to the hypothalamus can lead to various disorders like diabetes insipidus, growth hormone deficiency, altered temperature regulation, sleep disturbances, and emotional or behavioral changes.
The arcuate nucleus is a part of the hypothalamus in the brain. It is involved in the regulation of various physiological functions, including appetite, satiety, and reproductive hormones. The arcuate nucleus contains two main types of neurons: those that produce neuropeptide Y and agouti-related protein, which stimulate feeding and reduce energy expenditure; and those that produce pro-opiomelanocortin and cocaine-and-amphetamine-regulated transcript, which suppress appetite and increase energy expenditure. These neurons communicate with other parts of the brain to help maintain energy balance and reproductive function.
Cyclic peptides are a type of peptides in which the N-terminus and C-terminus of the peptide chain are linked to form a circular structure. This is in contrast to linear peptides, which have a straight peptide backbone with a free N-terminus and C-terminus. The cyclization of peptides can occur through various mechanisms, including the formation of an amide bond between the N-terminal amino group and the C-terminal carboxylic acid group (head-to-tail cyclization), or through the formation of a bond between side chain functional groups.
Cyclic peptides have unique structural and chemical properties that make them valuable in medical and therapeutic applications. For example, they are more resistant to degradation by enzymes compared to linear peptides, which can increase their stability and half-life in the body. Additionally, the cyclic structure allows for greater conformational rigidity, which can enhance their binding affinity and specificity to target molecules.
Cyclic peptides have been explored as potential therapeutics for a variety of diseases, including cancer, infectious diseases, and neurological disorders. They have also been used as tools in basic research to study protein-protein interactions and cell signaling pathways.
Pigmentation, in a medical context, refers to the coloring of the skin, hair, or eyes due to the presence of pigment-producing cells called melanocytes. These cells produce a pigment called melanin, which determines the color of our skin, hair, and eyes.
There are two main types of melanin: eumelanin and pheomelanin. Eumelanin is responsible for brown or black coloration, while pheomelanin produces a red or yellow hue. The amount and type of melanin produced by melanocytes can vary from person to person, leading to differences in skin color and hair color.
Changes in pigmentation can occur due to various factors such as genetics, exposure to sunlight, hormonal changes, inflammation, or certain medical conditions. For example, hyperpigmentation refers to an excess production of melanin that results in darkened patches on the skin, while hypopigmentation is a condition where there is a decreased production of melanin leading to lighter or white patches on the skin.
Adrenocorticotropic Hormone (ACTH) is a hormone produced and released by the anterior pituitary gland, a small endocrine gland located at the base of the brain. ACTH plays a crucial role in the regulation of the body's stress response and has significant effects on various physiological processes.
The primary function of ACTH is to stimulate the adrenal glands, which are triangular-shaped glands situated on top of the kidneys. The adrenal glands consist of two parts: the outer cortex and the inner medulla. ACTH specifically targets the adrenal cortex, where it binds to specific receptors and initiates a series of biochemical reactions leading to the production and release of steroid hormones, primarily cortisol (a glucocorticoid) and aldosterone (a mineralocorticoid).
Cortisol is involved in various metabolic processes, such as regulating blood sugar levels, modulating the immune response, and helping the body respond to stress. Aldosterone plays a vital role in maintaining electrolyte and fluid balance by promoting sodium reabsorption and potassium excretion in the kidneys.
ACTH release is controlled by the hypothalamus, another part of the brain, which produces corticotropin-releasing hormone (CRH). CRH stimulates the anterior pituitary gland to secrete ACTH, which in turn triggers cortisol production in the adrenal glands. This complex feedback system helps maintain homeostasis and ensures that appropriate amounts of cortisol are released in response to various physiological and psychological stressors.
Disorders related to ACTH can lead to hormonal imbalances, resulting in conditions such as Cushing's syndrome (excessive cortisol production) or Addison's disease (insufficient cortisol production). Proper diagnosis and management of these disorders typically involve assessing the function of the hypothalamic-pituitary-adrenal axis and addressing any underlying issues affecting ACTH secretion.
Skin pigmentation is the coloration of the skin that is primarily determined by two types of melanin pigments, eumelanin and pheomelanin. These pigments are produced by melanocytes, which are specialized cells located in the epidermis. Eumelanin is responsible for brown or black coloration, while pheomelanin produces a red or yellow hue.
The amount and distribution of melanin in the skin can vary depending on genetic factors, age, sun exposure, and various other influences. Increased production of melanin in response to UV radiation from the sun helps protect the skin from damage, leading to darkening or tanning of the skin. However, excessive sun exposure can also cause irregular pigmentation, such as sunspots or freckles.
Abnormalities in skin pigmentation can result from various medical conditions, including albinism (lack of melanin production), vitiligo (loss of melanocytes leading to white patches), and melasma (excessive pigmentation often caused by hormonal changes). These conditions may require medical treatment to manage or improve the pigmentation issues.
Leptin is a hormone primarily produced and released by adipocytes, which are the fat cells in our body. It plays a crucial role in regulating energy balance and appetite by sending signals to the brain when the body has had enough food. This helps control body weight by suppressing hunger and increasing energy expenditure. Leptin also influences various metabolic processes, including glucose homeostasis, neuroendocrine function, and immune response. Defects in leptin signaling can lead to obesity and other metabolic disorders.
Appetite regulation refers to the physiological and psychological processes that control and influence the desire to eat food. This complex system involves a variety of hormones, neurotransmitters, and neural pathways that work together to help maintain energy balance and regulate body weight. The hypothalamus in the brain plays a key role in appetite regulation by integrating signals from the digestive system, fat cells, and other organs to adjust feelings of hunger and fullness.
The hormones leptin and ghrelin are also important regulators of appetite. Leptin is released from fat cells and acts on the hypothalamus to suppress appetite and promote weight loss, while ghrelin is produced in the stomach and stimulates appetite and promotes weight gain. Other factors that can influence appetite regulation include stress, emotions, sleep patterns, and cultural influences.
Abnormalities in appetite regulation can contribute to the development of eating disorders such as anorexia nervosa, bulimia nervosa, and binge eating disorder, as well as obesity and other health problems. Understanding the mechanisms of appetite regulation is an important area of research for developing effective treatments for these conditions.
Neuropeptide Y (NPY) is a neurotransmitter and neuropeptide that is widely distributed in the central and peripheral nervous systems. It is a member of the pancreatic polypeptide family, which includes peptide YY and pancreatic polypeptide. NPY plays important roles in various physiological functions such as energy balance, feeding behavior, stress response, anxiety, memory, and cardiovascular regulation. It is involved in the modulation of neurotransmitter release, synaptic plasticity, and neural development. NPY is synthesized from a larger precursor protein called prepro-NPY, which is post-translationally processed to generate the mature NPY peptide. The NPY system has been implicated in various pathological conditions such as obesity, depression, anxiety disorders, hypertension, and drug addiction.
Cosyntropin is a synthetic form of adrenocorticotropic hormone (ACTH) that is used in medical testing to assess the function of the adrenal glands. ACTH is a hormone produced and released by the pituitary gland that stimulates the production and release of cortisol, a steroid hormone produced by the adrenal glands.
Cosyntropin is typically administered as an injection, and its effects on cortisol production are measured through blood tests taken at various time points after administration. This test, known as a cosyntropin stimulation test or ACTH stimulation test, can help diagnose conditions that affect the adrenal glands, such as Addison's disease or adrenal insufficiency.
It is important to note that while cosyntropin is a synthetic form of ACTH, it is not identical to the natural hormone and may have slightly different effects on the body. Therefore, it should only be used under the supervision of a healthcare professional.
Intraventricular injections are a type of medical procedure where medication is administered directly into the cerebral ventricles of the brain. The cerebral ventricles are fluid-filled spaces within the brain that contain cerebrospinal fluid (CSF). This procedure is typically used to deliver drugs that target conditions affecting the central nervous system, such as infections or tumors.
Intraventricular injections are usually performed using a thin, hollow needle that is inserted through a small hole drilled into the skull. The medication is then injected directly into the ventricles, allowing it to circulate throughout the CSF and reach the brain tissue more efficiently than other routes of administration.
This type of injection is typically reserved for situations where other methods of drug delivery are not effective or feasible. It carries a higher risk of complications, such as bleeding, infection, or damage to surrounding tissues, compared to other routes of administration. Therefore, it is usually performed by trained medical professionals in a controlled clinical setting.
Leptin receptors are cell surface receptors that bind to and respond to the hormone leptin. These receptors are found in various tissues throughout the body, including the hypothalamus in the brain, which plays a crucial role in regulating energy balance and appetite. Leptin is a hormone produced by adipose (fat) tissue that signals information about the size of fat stores to the brain. When leptin binds to its receptors, it activates signaling pathways that help regulate energy intake and expenditure, body weight, and glucose metabolism.
There are several subtypes of leptin receptors (LEPR), including LEPRa, LEPRb, LEPC, and LEPD. Among these, the LEPRb isoform is the most widely expressed and functionally important form. Mutations in the gene encoding the leptin receptor can lead to obesity, hyperphagia (excessive hunger), and impaired energy metabolism, highlighting the importance of this receptor in maintaining energy balance and overall health.
Melanocortin 2 receptor accessory protein - Wikipedia
Frontiers | The role of Neurochemicals, Stress Hormones and Immune System in the Positive Feedback Loops between Diabetes,...
Allgrove (AAA) Syndrome: Background, Pathophysiology, Etiology
Familial glucocorticoid deficiency: MedlinePlus Genetics
Obesity accelerates thymic aging
Melanocortin 3 receptor - wikidoc
Neonatal hyperpigmentation: Diagnosis of familial glucocorticoid deficiency with a novel mutation in the melanocortin-2...
Arthritic diseases: melanocortin type 3 receptor agonists as potential therapeutics : WestminsterResearch
Insulin resistance and type 2 diabetes in children
Pesquisa | Portal Regional da BVS
MC1R gene: MedlinePlus Genetics
Skill Checkup: Woman Gains Weight After Diet and Exercise
Publications
Zalfa A. Abdel-Malek, PhD
rs12970134 - SNPedia
Hypothalamus News, Research - Page 38
Items for Psychology in 2007 : Sussex Research Online
Treating the Obese Diabetic
Evolution of melanocortin receptors in teleost fish: the melanocortin type 1 receptor - Institut de Génomique Fonctionnelle de...
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MELANOTAN 2 10MG
Novel drug makes mice skinny even on sugary, fatty diet | ScienceDaily
Melanotan 2 Dosage Calculator and Chart | A-Z Guide
Allgrove (AAA) Syndrome Clinical Presentation: History, Physical, Causes
The Battle of the Bulge: Targeting MC4R for Obesity Treatment
Antiobesity pharmacotherapy: new drugs and emerging targets
Jeffrey E. Pessin - Publications - Albert Einstein College of Medicine
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MC4R14
- PMID 22869321 ] Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals. (snpedia.com)
- Nonetheless, it had no impact on the body's natural glucose production, suggesting that the activation of MC3R and MC4R receptors in the central nervous system affected insulin sensitivity in a tissue-specific manner, independently [2]. (pinnaclepeptides.com)
- One prominent genetic factor associated with obesity is the melanocortin 4 receptor (MC4R). (pharmacymarketonline.net)
- MC4R is a G-protein-coupled receptor expressed in key areas of the brain, such as the hypothalamus, brainstem, and other regions involved in appetite regulation. (pharmacymarketonline.net)
- Scientists have discovered a connection between loss-of-function mutations in MC4R and metabolic syndrome, type 2 diabetes, and cardiovascular disease. (pharmacymarketonline.net)
- Activation of MC4R has been found to reduce body weight and increase energy expenditure in non-human primates, suggesting its potential as a therapeutic strategy for obesity[2]. (pharmacymarketonline.net)
- A well-studied example of this is melanocortin 4 receptor (MC4R), mutations in which are the most common cause of human monogenic obesity. (inforang.com)
- 5 Mutations in leptin (LEP) and its receptor (LEPR), melanocortin 4 receptor (MC4R), pro-opiomelanocortin (POMC), prohormone convertase 1 (PCSK1), brain-derived neurotrophic factor (BDNF), neurotrophic tyrosine kinase receptor type 2 (NTRK2), and single-minded homolog 1 (SIM1) have all been shown to influence appetite and weight gain. (bariatrictimes.com)
- 7,8 MC4R is a receptor in this axis, and POMC encodes the precursor polypeptide that acts on this receptor, which must first be processed by PCSK1. (bariatrictimes.com)
- 5,9 BDNF, its receptor NTRK2, and SIM1 are known downstream targets of MC4R signaling, yet their exact actions are still being elucidated. (bariatrictimes.com)
- Patients with mutations in MC4R have undergone weight loss surgery, including Roux-en-Y gastric bypass, sleeve gastrectomy, and gastric banding. (bariatrictimes.com)
- 3 In patients with heterozygous MC4R mutations, reported results were comparable to wild type MC4R patients, with 60 percent excess weight loss reported following gastric bypass and 48 percent excess weight loss reported following gastric banding, although these results are from small cohorts. (bariatrictimes.com)
- 4 receptor (MC4R) agonist setmelanotide as a treatment option in rare obesity syndromes. (eurospe.org)
- Melanocortin pathways, consisting of POMC neurons that produce a- MSH and downstream MC3 and 4 receptor (MC4R)-containing neurons, are critical for these processes. (grantome.com)
Agonist10
- Conversely, the D 2 R agonist bromocriptine, which has been used for over 40 years to treat Parkinson's disease and hyperprolactinemia ( 6 ), was found to lower blood glucose levels and improve insulin sensitivity in patients with T2DM ( 7 ). (frontiersin.org)
- The effect of the selective human MC3 receptor agonist PG992 on high density human chondrocyte micromass cultures activated by IL-1beta. (westminster.ac.uk)
- Recently, the FDA approved tirzepatide , glucose-dependent insulinotropic polypeptide (GIP) receptor and GLP-1 receptor agonist, for chronic weight maintenance in adults with obesity. (medscape.com)
- The selective 5-HT 2C receptor agonist lorcaserin was approved by the FDA in 2012 but was taken off the market in 2020 because of potential cancer risk. (medscape.com)
- Arena Pharmaceuticals, CA, USA), approved in June 2012 by the FDA but still under review by the EMA, is a selective agonist at the G-protein coupled 5HT 2c receptor. (medscape.com)
- Co-injection of corticotropinreleasing factor (CRF), the agonist of corticotropin releasing hormone receptor 1 (CRHR1), suppressed feeding behaviour in a MRAP2-dependent manner. (bvsalud.org)
- Melanotan II is a non-selective agonist of melanocortin receptors. (pinnaclepeptides.com)
- Flibanserin is a daily, on-demand serotonin drug with mixed receptor agonist and antagonistic effects that improves overall sexual desire. (medscape.com)
- Discovery of a novel potent peptide agonist to adiponectin receptor 1. (phoenixpeptide.com)
- A potent peptide as adiponectin receptor 1 agonist to against fibrosis. (phoenixpeptide.com)
Mutations6
- Patients with isolated familial glucocorticoid deficiency (type 1 FGD) have mutations in the melanocortin-2 (ACTH) receptors. (medscape.com)
- MC2R gene mutations lead to the production of a receptor that cannot be transported to the cell membrane or, if it does get to the cell membrane, cannot bind to ACTH. (medlineplus.gov)
- MRAP gene mutations impair the transport of the ACTH receptor to the cell membrane. (medlineplus.gov)
- Phase II Study of Afatinib in Patients With Tumors With Human Epidermal Growth Factor Receptor 2-Activating Mutations: Results From the National Cancer Institute-Molecular Analysis for Therapy Choice ECOG-ACRIN Trial (EAY131) Subprotocol EAY131-B. (cdc.gov)
- Patients with Allgrove syndrome (type 2 FGD) have no mutations in the coding sequence or the promoter region of this receptor gene. (medscape.com)
- Conversely, gain-of-function mutations are associated with lower BMI, reduced obesity, and decreased risks of type 2 diabetes and coronary artery disease[1]. (pharmacymarketonline.net)
MC1R8
- The MC1R gene provides instructions for making a protein called the melanocortin 1 receptor. (medlineplus.gov)
- These MC1R polymorphisms reduce the ability of the melanocortin 1 receptor to stimulate eumelanin production, causing melanocytes to make mostly pheomelanin. (medlineplus.gov)
- Certain variations in the MC1R gene increase the risk of developing melanoma, a type of skin cancer that begins in melanocytes. (medlineplus.gov)
- Certain genetic changes in the MC1R gene modify the appearance of people with oculocutaneous albinism type 2. (medlineplus.gov)
- Defining the quantitative contribution of the melanocortin 1 receptor (MC1R) to variation in pigmentary phenotype. (medlineplus.gov)
- My research is focused on investigating the function of the melanocortin 1 receptor (MC1R) , its agonists α-melanocyte stimulating hormone (α-MSH) and ACTH, and antagonists agouti signaling protein and human β-defensin 3 in regulating cutaneous pigmentation and the response to UV radiation. (uc.edu)
- We were among the first to demonstrate that human melanocytes express functional MC1R and that activation of this receptor is critical for the melanogenic (i.e. tanning response) to UV. (uc.edu)
- BACKGROUND: The melanocortin receptor accessory proteins (MRAP1 and MRAP2) are well-known endocrine regulators for the trafficking and signalling of all five melanocortin receptors (MC1R-MC5R). (bvsalud.org)
Agonists7
- Glucagon-like peptide-1 (GLP-1) agonists have been shown to promote weight loss in patients with or without type 2 diabetes and are the Food and Drug Administration (FDA)-approved for chronic weight management . (medscape.com)
- Melanocortin-4 receptor agonists are approved for weight management in patients with rare genetic conditions (ie, proopiomelanocortin, proprotein convertase subtilisin/kexin type 1, and leptin receptor deficiencies). (medscape.com)
- Crinetics presented a late-breaking e-poster describing the potential of SST5 receptor agonists to regulate glucose-stimulated insulin secretion from human islet cells. (crinetics.com)
- One of somatostatin's roles in maintaining blood glucose concentrations is to regulate insulin secretion, yet the lack of highly selective agonists has previously hampered efforts to identify the role of the individual somatostatin receptor subtypes in this process. (crinetics.com)
- In its preclinical efforts, Crinetics observed that SST5 receptor agonists were potent inhibitors of insulin secretion in the healthy pancreas and under conditions that stimulate excess insulin secretion. (crinetics.com)
- These findings suggest that AdipoRs' agonists could be developed into a potential therapeutic agent for metabolic diseases, such as diabetes mellitus, especially for type II diabetes, a long-term metabolic disorder characterized by high blood sugar, insulin resistance, and relative lack of insulin. (phoenixpeptide.com)
- Based on crystal structure of AdipoR1, we designed AdipoR1's peptide agonists using protein-peptide docking simulation and screened their receptor binding abilities and biological functions via surface plasmon resonance (SPR) and biological analysis. (phoenixpeptide.com)
Associated with obesity1
- Polycystic ovary syndrome (PCOS) is considered as a risk factor for diabetes type 2 (DM2), it is often associated with obesity, β-cell dysfunction or insulin resistance. (endocrine-abstracts.org)
Human melanocortin1
- T. J. Park, S. S. Choi, G. A. Gang, Y. Kim, High-Level Expression and Purification of the Second Transmembrane Domain of Wild-Type and Mutant Human Melanocortin-4 Receptor for Solid-State NMR Structural Studies, Protein Expression and Purification, Volume 62, (Issue 2), December 2008, Pages 139-145. (praiseworthyprize.org)
Melanocyte-stimula4
- This gene encodes MC 3 , a G-protein coupled receptor for melanocyte-stimulating hormone and adrenocorticotropic hormone that is expressed in tissues other than the adrenal cortex and melanocytes. (wikidoc.org)
- Activation of this receptor has previously been shown to decrease hunger and increase satiety, [ 89 ] the mechanism of which has been proposed to be by increasing pro-opiomelanocortin (POMC) expression with subsequent increased release of α-melanocyte stimulating hormone, which stimulates the anorexigenic melanocortin 4 receptor. (medscape.com)
- Melanotan 2 is a synthetic peptide that mimics alpha-melanocyte-stimulating hormone (α-MSH), a naturally occurring substance secreted from the pituitary gland [ 1 ]. (peptides.org)
- Melanotan 2 is a small efficient molecule as compared to the linear original Melanotan I design after natural melanocyte stimulating hormone peptide. (osgear.se)
ACTH8
- The interaction between MCs and MRAP was found to reduce the former response to the melanocortin synthetic ligand NDP-MSH The familial glucocorticoid deficiency occurs as a result of poor adrenal response to ACTH stimulation which leads to glucocorticoid deficiency. (wikipedia.org)
- The MC2R gene provides instructions for making a protein called adrenocorticotropic hormone (ACTH) receptor, which is found primarily in the adrenal glands. (medlineplus.gov)
- The protein produced from the MRAP gene transports the ACTH receptor from the interior of the cell to the cell membrane. (medlineplus.gov)
- When the ACTH receptor is embedded within the cell membrane, it is turned on (activated) by the MRAP protein. (medlineplus.gov)
- Activated ACTH receptor can then attach (bind) to ACTH, and this binding triggers the adrenal glands to produce glucocorticoids . (medlineplus.gov)
- Without the binding of the ACTH receptor to its hormone, there is no signal to trigger the adrenal glands to produce glucocorticoids. (medlineplus.gov)
- Therefore, identification of novel endogenous targets for drug development may have beneficial properties ACTH4-10, a heptapeptide fragment derived from the hormone adrenocorticotrophin (ACTH) modulates the inflammatory response in a corticosterone-independent manner, via agonism at melanocortin type 3 receptors (MC3-R) expressed on peritoneal macrophages. (westminster.ac.uk)
- Recent studies from our group on melanocortin 2 receptors (Mc2r) from basal families of actinopterygians have served to resolve that Mrap1 dependence and ACTH selectivity are features of even the most basal ray-finned fishes. (bvsalud.org)
Variants2
- Genetic variants of MRAP are linked to an autosomal recessive condition called Familial Glucocorticoid Deficiency type 2 (FGD-2). (wikipedia.org)
- The aim of the current study was to evaluate the association of these 2 variants with glioma susceptibility using a meta-analysis approach. (geneticsmr.com)
Diabetes mellitus6
- Type 2 diabetes mellitus (T2DM) and depression are significant public health and socioeconomic issues. (frontiersin.org)
- Soon after the introduction of atypical antipsychotics, which antagonize serotonin receptors and dopamine D 2 receptors (D 2 R), numerous case reports appeared showing that the use of these drugs were associated with increased obesity and the development of type 2 diabetes mellitus (T2DM) ( 5 ). (frontiersin.org)
- In recent decades, the world has seen expanding waistlines in expanding numbers, and with this, an increased prevalence of metabolic syndrome, a collection of risk factors predisposing toward cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM). (bariatrictimes.com)
- In previous studies, we have constructed a predictive model for the classification of AD patients based on levels of circulating steroids and their polar conjugates.Both AD and Type 2 diabetes mellitus(T2DM) are well known to affect the levels of some steroid hormones, however, in the opposite direction, and in a gen. (endocrine-abstracts.org)
- Introduction: Melatonin is a crucial hormone for controlling sleep rhythms and disruption of its natural secretory rhythmicity is considered to be one of the causes of type 2 diabetes mellitus. (endocrine-abstracts.org)
- The identification of genomic determinants responsible for common multifactorial diseases like type 2 diabetes mellitus (T2DM) is facilitated in large families from relatively genetically-isolated populations and can extend results from GWS based on a case control cohort to detect rare alleles with strong effects. (endocrine-abstracts.org)
Homeostasis2
- Significance of the Melanocortin 1 and Endothelin B Receptors in Melanocyte Homeostasis and Prevention of Sun-Induced Genotoxicity. (uc.edu)
- Since the discovery of two leptin deficient children in 1997, investigations into these disorders have focused on the Leptin-Melanocortin pathway and its regulation of appetite and energy homeostasis. (bariatrictimes.com)
Deficiency3
- There are multiple types of familial glucocorticoid deficiency, which are distinguished by their genetic cause. (medlineplus.gov)
- Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2. (medlineplus.gov)
- Furthermore, the obesity induced by melanocortin 4 receptor deficiency also constricted the T-cell repertoire diversity, recapitulating the thymic defects observed with diet-induced obesity. (nih.gov)
Obesity and type 2 diabet3
- Liver and adipose (fat) tissues in the rodents showed no evidence of fatty liver disease, a complication related to poor diet, obesity and type 2 diabetes. (sciencedaily.com)
- The rationale for these studies is that they will be the first to address whether diabetes is accompanied by defective melanocortin signaling that may cause or exacerbate ED. The rising number of men with obesity and type 2 diabetes makes this research highly significant. (grantome.com)
- Defective crosstalk between the brain and peripheral organs contributes to the development of obesity and type 2 diabetes. (nature.com)
Serotonin1
- 5 The anorexigenic effect of monoamine serotonin is also mediated by the 5HT-2C receptor in POMC neurons. (nature.com)
Regulates2
- Wilhelm F, Kässner F, Schmid G, Kratzsch J, Laner A, Wabitsch M, Körner A, Kiess W, Garten A: Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytes. (uniklinikum-leipzig.de)
- PMID 21736789 ] A variant near the melanocortin-4 receptor gene regulates postprandial lipid metabolism in a healthy Caucasian population. (snpedia.com)
Modulate2
- In addition to regulating MC2 surface expression and signalling, MRAP was found to modulate the function of the other melanocortin receptors. (wikipedia.org)
- Sweating is dependent on our cannabinoid system (CS): for example, CB2 skin receptors modulate/maintain mammalian body temperature. (bryanwilliambrickner.com)
Pigmentation2
- This receptor plays an important role in normal pigmentation. (medlineplus.gov)
- Melanotan peptides Melanotan II binds to melanocortin receptors influencing pigmentation, inflammation, energy, appetite and sexual function. (osgear.se)
Insulin6
- Stimulation of a receptor in the brain that controls insulin responses has been shown to halt or diminish the neurodegeneration of Alzheimer's disease, providing evidence that the disease can be treated in its early stages, according to a study by researchers at Rhode Island Hospital and Brown Medical School. (news-medical.net)
- 1,2 Within this pandemic, there are patients who are outliers in the development and progression of obesity and insulin resistance. (bariatrictimes.com)
- IGF-2 is a member of the insulin family of polypeptide growth factors that is involved in development and growth. (canpeptides.com)
- This hypothesis has been formulated on the basis of strong preliminary data produced in the applicants' laboratories and will be tested with three specific aims: 1) Determine whether impaired insulin and leptin signaling in POMC neurons alters erectile function, 2) Determine whether restoring neuronal insulin and leptin sensitivity and a-MSH production improves sexual performance, and 3) Determine whether downstream oxytocin circuitry mediates the effects of a-MSH on erectile function. (grantome.com)
- Under the first aim, novel cell type-specific tools will be used to allow acute neuronal manipulation to examine the role of POMC-specific insulin and leptin resistance in ED in a unique mouse model of prediabetes. (grantome.com)
- Longitudinal changes in risk variables of insulin resistance syndrome from childhood to young adulthood in offspring of parents with type 2 diabetes: the Bogalusa Heart Study. (medigraphic.com)
Polymorphism1
- The melatonin receptor gene polymorphism rs10830963 is not associated with significant differences in sleep patterns and biorhythms. (endocrine-abstracts.org)
Neurons1
- Mouse models of cell type-specific cilia dysgenesis have subsequently demonstrated that ciliary defects restricted to specific hypothalamic neurons are sufficient to induce obesity and hyperphagia. (inforang.com)
Activation2
- Single- and partial-alanine substitutions of the HFRW and KKRRP motifs varied in their impacts on receptor-ligand affinity from having no effect to completely inhibiting lfMc2r activation. (bvsalud.org)
- Activation of adiponectin receptors (AdipoRs) by its natural ligand, adiponectin has been known to be involved in modulating critical metabolic processes such as glucose metabolism and fatty acid oxidation as demonstrated by a number of in vitro and in vivo studies over last two decades. (phoenixpeptide.com)
MC2R1
- We support this interpretation with a molecular clock analysis of the melanocortin receptors, which demonstrates the uniquely high rate of sequence divergence in Mc2r. (bvsalud.org)
Selective1
- Additionally, other selective 5-HT 2C receptors were withdrawn from the market as well owing to unwanted effects, such as higher risk for cardiac valvular abnormalities . (medscape.com)
Dopamine1
- Bremelanotide is given on demand and works through the dopamine melanocortin system to improve sexual receptiveness and response of sexual desires in event-related experience. (medscape.com)
Encodes1
- The MTNR1B gene encodes the melatonin receptor. (endocrine-abstracts.org)
Melanoma2
- Melanocortins and the melanocortin 1 receptor, moving translationally towards melanoma prevention. (uc.edu)
- The estimated lifetime risk of being diagnosed with melanoma skin cancer is 1 in 36 (3%) for males, and 1 in 47 (2%) for females born after 1960 in the UK. (cancerresearchuk.org)
Mutation2
- The patient was found to be homozygous for a novel mutation in the melanocortin-2 receptor gene (635insC, I154H). (tau.ac.il)
- Functional analysis of a proline to serine mutation in codon 453 of the thyroid hormone receptor 1 gene. (zayiflama.org)
MC3R1
- Melanocortin receptor 3 is a protein that in humans is encoded by the MC3R gene . (wikidoc.org)
Binds1
- Specifically, α-MSH binds to a set of receptors called melanocortin receptors [ 2 ]. (peptides.org)
Lorcaserin1
- The BLOOM-DM study was a 1-year RCT in Type 2 diabetics taking metformin or SU, or both, comparing placebo with 10 mg lorcaserin daily (q.d.) versus lorcaserin 10 mg twice daily (b.i.d. (medscape.com)
Melanotropin1
- For people with sun allergies/mutated receptors, synthetic melanotropin peptide supplements offer life changing opportunity. (osgear.se)
Biochemistry1
- J. Hoppe, H. A. Weich, W. Eichner, Preparation of Biologically Active Platelet-Derived Growth Factor Type Bb from a Fusion Protein Expressed in Escherichia coli, Biochemistry, Volume 28, (Issue 7), April 1989, Pages 2956-2960. (praiseworthyprize.org)
Basal1
- [ 3 , 7 ] In patients with Allgrove syndrome, dermal fibroblasts have higher basal intracellular reactive oxygen species and are more sensitive to oxidative stress than wild-type fibroblasts. (medscape.com)
Functional1
- Garcia-Borron JC, Sanchez-Laorden BL, Jimenez-Cervantes C. Melanocortin-1 receptor structure and functional regulation. (medlineplus.gov)
Synthetic2
Regulation of appetite and energy1
- A potential mechanism underlying hypothalamic neuron cilia-related obesity is impaired ciliary localization of G protein-coupled receptors involved in the regulation of appetite and energy metabolism. (inforang.com)
Hypothalamus1
- 6,7 Leptin is a hormone secreted by adipose tissue which, when bound to its receptor in the arcuate nucleus of the hypothalamus, signals satiety through the melanocortin axis. (bariatrictimes.com)
Stimulation4
- MC1 Receptor is located on the melanocytes and its stimulation by MT-II causes darkening of skin and hair. (pinnaclepeptides.com)
- Leptin receptors traffic to the periciliary area upon leptin stimulation. (inforang.com)
- Women do not feel aroused by any type of sexual genital or nongenital stimulation (eg, kissing, dancing, watching an erotic video, physical stimulation), despite the occurrence of physical genital response (eg, genital congestion). (msdmanuals.com)
- Subjective arousal in response to any type of sexual stimulation is absent or low, and women report absence of physical genital arousal (ie, they report the need of external lubricants and may state they know that swelling of the clitoris no longer occurs). (msdmanuals.com)
Proteins2
- J. C. Rodriguez, L. Wong, P. A. Jennings, The Solvent in CNBr Cleavage Reactions Determines the Fragmentation Efficiency of Ketosteroid Isomerase Fusion Proteins Used in the Production of Recombinant Peptides, Protein Expression and Purification, Volume 28, (Issue 2), April 2003, Pages 224-231. (praiseworthyprize.org)
- Also, SPR and virtual screening techniques utilized in this study may potentially be applied to other peptide-drug screening processes against membrane receptor proteins. (phoenixpeptide.com)
Melanotan 2 Dosage2
- Research into sunless tanning is on the rise, with many researchers looking to establish the correct melanotan 2 dosage for their next experiment. (peptides.org)
- We have compiled this informative melanotan 2 dosage calculator and guide to highlight key findings concerning how this peptide has been dosed in past trials. (peptides.org)
Autonomic1
- [ 2 ] Specific autonomic disturbances described in this syndrome include abnormal pupillary reflexes, poor heart rate variability, and orthostatic hypotension. (medscape.com)
Therapeutics1
- However, therapeutics targeting MC receptors have the disadvantage of altering blood pressure and heart rate. (grantome.com)
Stimulates1
- Peptide Hormone Therapy: Melanotan stimulates melanin, particularly low fitzpatrick types. (osgear.se)
Protein4
- Melanocortin 2 receptor accessory protein is a transmembrane accessory protein that in humans is encoded by the MRAP gene located in chromosome 21q22.11. (wikipedia.org)
- MRAP is an accessory protein to a family of five receptors called the melanocortin receptors (MC1-5). (wikipedia.org)
- The protein is made of three domains: a transmembrane domain that is responsible for the attachment of the MRAP molecule in the cell membrane and facilitates the interaction with the receptor. (wikipedia.org)
- The observation of MRAP2 on regulating several non-melanocortin G protein-coupled receptors (GPCRs) has been sporadically reported, whereas other endogenous GPCR partners of the MRAP protein family are largely unknown. (bvsalud.org)
Regulate1
- Alternatively, this disorder may represent a dysfunction of melanocortin receptor signaling, as melanocortin receptors are known to regulate adrenal function and skin exocrine gland function. (medscape.com)
Appetite2
- GLP-1 is a physiologic regulator of appetite and calorie intake, and the GLP-1 receptor is present in several areas of the brain involved in appetite regulation. (medscape.com)
- University of Florida researchers have discovered the appetite-controlling hormone leptin could also combat type 2 diabetes, a disease that has become a growing problem in the United States as more Americans pack on extra pounds. (news-medical.net)
Alzheimer's1
- Exploiting formyl peptide receptor 2 to promote microglial resolution: a new approach to Alzheimer's disease treatment. (westminster.ac.uk)
Melanocytes6
- The receptor is primarily located on the surface of melanocytes, which are specialized cells that produce a pigment called melanin. (medlineplus.gov)
- The melanocortin 1 receptor controls which type of melanin is produced by melanocytes. (medlineplus.gov)
- When the receptor is activated, it triggers a series of chemical reactions inside melanocytes that stimulate these cells to make eumelanin. (medlineplus.gov)
- If the receptor is not activated or is blocked, melanocytes make pheomelanin instead of eumelanin. (medlineplus.gov)
- The melanocortin 1 receptor is also active in cells other than melanocytes, including cells involved in the body's immune and inflammatory responses. (medlineplus.gov)
- These variations reduce the ability of the melanocortin 1 receptor to stimulate eumelanin production in melanocytes, resulting in fair skin. (medlineplus.gov)
Amino acid1
- Melanotan 2 has a small protective amino acid structure that effects the melanocortin 1, 3, 4 and 5 receptors. (osgear.se)
Potent1
- Reconstituted with bacteriostatic water, Melanotan 2 research peptide remains potent and preserved. (osgear.se)
Erectile Dysfunction1
- Erectile dysfunction (ED) is a frequent complication of type 2 diabetes that impairs quality of life for up to 75% of men with diabetes. (grantome.com)
Cell membrane1
- MRAP assists in the transport of the melanocortin 2 receptor to the cell membrane from the endoplasmic reticulum and assist in the generation of cAMP by the activated receptor. (wikipedia.org)
Peptide3
- Melanotan 2 is a freeze dried peptide sealed in a sterile multi-use vial. (osgear.se)
- Reconstituting Melanotan 2 peptide is a necessity and will require proper due diligence for results. (osgear.se)
- Mixing Melanotan 2: 1-2ml Bacteriostatic water reconstitutes and preserves tanning peptide Melanotan best. (osgear.se)
Intake1
- The his- Bariatric surgery reduces the size of the stomach, increases tory of dietary supplements is full of success stories in terms the feeling of fullness, and reduces the amount of food intake.8 of efficacy, but this success is matched by tragedy with regard Different types of bariatric surgery include the following: to safety. (eddoctor24h.com)
Cardiovascular4
- It is correlated with several metabolic and cardiovascular complications in both adults and children [ 1 , 2 ]. (e-apem.org)
- The familiar results of this stress are obesity, type 2 diabetes and cardiovascular complications. (sciencedaily.com)
- As our living standards improve and dietary patterns change, the prevalence of obesity has increased, leading to a range of health complications such as type 2 diabetes, fatty liver disease, and cardiovascular disorders. (pharmacymarketonline.net)
- Goran MI, Ball GDC, Cruz ML. Obesity and risk of type 2 diabetes and cardiovascular disease in children and adolescents. (medigraphic.com)
Molecular1
- (2) Molecular Biophysics Laboratory, Department of Biological Sciences, Indian Institute of Science Education and Research Bhopal, Transit campus : ITI (Gas Rahat) Building, Govindpura, Bhopal 462023. (praiseworthyprize.org)