Peptide YY |
PDB rendering based on 1qbf.
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Available structures |
PDB |
Ortholog search: PDBe, RCSB |
List of PDB id codes |
2DEZ, 2DF0, 2L60
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Identifiers |
Symbols |
PYY ; PYY-I; PYY1 |
External IDs |
OMIM: 600781 MGI: 99924 HomoloGene: 3066 GeneCards: PYY Gene |
Gene ontology |
Molecular function |
• G-protein coupled receptor binding
• hormone activity
• neuropeptide hormone activity
• protein binding
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Cellular component |
• extracellular region
• extracellular space
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Biological process |
• movement of cell or subcellular component
• cytoskeleton organization
• G-protein coupled receptor signaling pathway
• neuropeptide signaling pathway
• cell-cell signaling
• digestion
• feeding behavior
• cell proliferation
• regulation of appetite
• eating behavior
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Sources: Amigo / QuickGO |
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Orthologs |
Species |
Human |
Mouse |
Entrez |
5697 |
217212 |
Ensembl |
ENSG00000131096 |
ENSMUSG00000017311 |
UniProt |
P10082 |
Q9EPS2 |
RefSeq (mRNA) |
NM_004160 |
NM_145435 |
RefSeq (protein) |
NP_004151 |
NP_663410 |
Location (UCSC) |
Chr 17:
43.95 – 44 Mb |
Chr 11:
102.11 – 102.11 Mb |
PubMed search |
[1] |
[2] |
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Peptide YY (PYY) also known as peptide tyrosine tyrosine or pancreatic peptide YY3-36 is a peptide that in humans is encoded by the PYY gene.[1] Peptide YY is a short (36-amino acid) peptide released by cells in the ileum and colon in response to feeding. In the blood, gut, and other elements of periphery, PYY acts to reduce appetite; but when injected directly into the central nervous system, PYY is anorexigenic, i.e., it decreases appetite.[2]
Peptide YY can be produced as the result of enzymatic breakdown of crude fish proteins and ingested as a food product.[3]
Contents
- 1 Structure
- 2 Release
- 3 Function
- 4 Animal studies
- 5 Relevance to obesity
- 6 See also
- 7 References
- 8 Further reading
- 9 External links
Structure
Peptide YY is related to the pancreatic peptide family by having 18 of its 36 amino acids located in the same positions as pancreatic peptide.[4] The two major forms of peptide YY are PYY1-36 and PYY3-36, which have PP fold structural motifs. However, the most common form of circulating PYY immunoreactivity is PYY3-36, which binds to the Y2 receptor (Y2R) of the Y family of receptors.[5] Peptide YY3-36 (PYY) is a linear polypeptide consisting of 36 amino acids with structural homology to NPY and pancreatic polypeptide.
Release
PYY is found in L cells in the mucosa of gastrointestinal tract, especially in ileum and colon. Also, a small amount of PYY, about 1-10%, is found in the esophagus, stomach, duodenum and jejunum.[6] PYY concentration in the circulation increases postprandially (after food ingestion) and decreases by fasting.[5] In addition, PYY is produced by a discrete population of neurons in the brainstem, specifically localized to the gigantocellular reticular nucleus of the medulla oblongata.[7] C. R. Gustavsen et al. had found PYY-producing cells located in the islets of Langerhans in rats. They were observed either alone or co-localized with glucagon or PP.[8]
Function
PYY exerts its action through NPY receptors; it inhibits gastric motility and increases water and electrolyte absorption in the colon.[9] PYY may also suppress pancreatic secretion. It is secreted by the neuroendocrine cells in the ileum and colon in response to a meal, and has been shown to reduce appetite. PYY works by slowing the gastric emptying; hence, it increases efficiency of digestion and nutrient absorption after a meal. Research has also indicated PYY may be useful in removing aluminium accumulated in the brain.[citation needed]
Animal studies
Several studies have shown acute peripheral administration of PYY3-36 inhibits feeding of rodents and primates. Other studies on Y2R-knockout mice have shown no anorectic effect on them. These findings indicate PYY3-36 has an anorectic (losing appetite) effect, which is suggested to be mediated by Y2R. PYY-knockout female mice increase in body weight and fat mass. PYY-knockout mice, on the other hand, are resistant to obesity, but have higher fat mass and lower glucose tolerance when fed a high-fat diet, compared to control mice. Thus, PYY also plays a very important role in energy homeostasis by balancing food intake.[5] PYY oral spray was found to promote fullness.[10] Viral gene therapy of the salivary glands resulted in long-term intake reduction.[11]
Relevance to obesity
Leptin also reduces appetite in response to feeding, but obese people develop a resistance to leptin. Obese people secrete less PYY than non-obese people,[12] and attempts to use PYY directly as a weight-loss drug have met with some success. Researchers noted the caloric intake during a buffet lunch offered two hours after the infusion of PYY was decreased by 30% in obese subjects (P<0.001) and 31% in lean subjects (P<0.001).[13]
While some studies have shown obese persons have lower circulating level of PYY postprandially, other studies have reported they have normal sensitivity to the anorectic effect of PYY3-36. Thus, reduction in PYY sensitivity may not be one of the causes of obesity, in contrast to the reduction of leptin sensitivity. The anorectic effect of PYY could possibly be a future obesity drug.[5]
The consumption of protein boosts PYY levels, so some benefit was observed in experimental subjects in reducing hunger and promoting weight loss.[14] This would help explain the weight-loss experienced with high-protein diets.
Obese patients undergoing gastric bypass showed marked metabolic adaptations, resulting in frequent diabetes remission 1 year later. When the confounding of calorie restriction is factored out, β-cell function improves rapidly, very possibly under the influence of enhanced GLP-1 responsiveness. Insulin sensitivity improves in proportion to weight loss, with a possible involvement of PYY.[15]
See also
References
- ^ EntrezGene 5697
- ^ Woods S. C., D'Alessio D. A. (2008). "Central control of body weight and appetite". J Clin Endocrinol Metab 93 (11 Suppl 1): S37–50. doi:10.1210/jc.2008-1630.
- ^ http://www.bio.umass.edu/biology/mccormick/pdf/Murashita%20et%20al%202009.pdf
- ^ DeGroot, Leslie Jacob (1989). J. E. McGuigan, ed. Endocrinology. Philadelphia: Saunders. p. 2754. ISBN 0-7216-2888-5.
- ^ a b c d Murphy KG, Bloom SR (December 2006). "Gut hormones and the regulation of energy homeostasis". Nature 444 (7121): 854–9. doi:10.1038/nature05484. PMID 17167473.
- ^ Taylor IL (March 1985). "Distribution and release of peptide YY in dog measured by specific radioimmunoassay". Gastroenterology 88 (3): 731–7. PMID 3838162.
- ^ Glavas MM, Grayson BE, Allen SE, Copp DR, Smith MS, Cowley MA, Grove KL (2008). "Characterization of brainstem peptide YY (PYY) neurons". J Comp Neurol 506 (2): 194–210. doi:10.1002/cne.21543. PMID 18022952.
- ^ Gustavsen CR, Pillay N, Heller RS (2008). "An immunohistochemical study of the endocrine pancreas of the African ice rat, Otomys sloggetti robertsi". Acta Histochem. 110 (4): 294–301. doi:10.1016/j.acthis.2007.11.003. PMID 18406449.
- ^ Liu C, Aloia T, Adrian T, Newton T, Bilchik A, Zinner M, Ashley S, McFadden D (1996). "Peptide YY: a potential proabsorptive hormone for the treatment of malabsorptive disorders". Am Surg 62 (3): 232–6. PMID 8607584.
- ^ "UF researchers use oral peptide spray to stimulate weight loss in animals". Dec 19, 2013.
- ^ "Salivary PYY: a putative bypass to satiety.". PLOS ONE 6: e26137. 2011. doi:10.1371/journal.pone.0026137. PMID 22028819.
- ^ Alvarez Bartolomé M, Borque M, Martinez-Sarmiento J, Aparicio E, Hernández C, Cabrerizo L, Fernández-Represa JA (June 2002). "Peptide YY secretion in morbidly obese patients before and after vertical banded gastroplasty". Obes Surg 12 (3): 324–7. doi:10.1381/096089202321088084. PMID 12082881.
- ^ Batterham RL, Cohen MA, Ellis SM, Le Roux CW, Withers DJ, Frost GS, Ghatei MA, Bloom SR (September 2003). "Inhibition of food intake in obese subjects by peptide YY3-36". The New England Journal of Medicine 349 (10): 941–8. doi:10.1056/NEJMoa030204. PMID 12954742.
- ^ Batterham RL, Heffron H, Kapoor S, Chivers J, Chandarana K, Herzog H, Le Roux CW, Thomas EL, Bell JD, Withers DJ (2006). "Critical role for peptide YY in protein-mediated satiation and body-weight regulation". Cell Metabolism 4 (3): 223–233. doi:10.1016/j.cmet.2006.08.001. PMID 16950139.
- ^ Nannipieri M, Baldi S, Mari A, Colligiani D, Guarino D, Camastra S, Barsotti E, Berta R, Moriconi D, Bellini R, Anselmino M, Ferrannini E (November 2013). "Roux-en-Y Gastric Bypass and Sleeve Gastrectomy: Mechanisms of Diabetes Remission and Role of Gut Hormones". J. Clin. Endocrinol. Metab. 98 (11): 4391–9. doi:10.1210/jc.2013-2538. PMID 24057293.
Further reading
- Ekblad E, Sundler F (2002). "Distribution of pancreatic polypeptide and peptide YY". Peptides 23 (2): 251–61. doi:10.1016/S0196-9781(01)00601-5. PMID 11825640.
- Sandström O, El-Salhy M (2002). "Ontogeny and the effect of aging on pancreatic polypeptide and peptide YY". Peptides 23 (2): 263–7. doi:10.1016/S0196-9781(01)00603-9. PMID 11825641.
- Yang H (2002). "Central and peripheral regulation of gastric acid secretion by peptide YY". Peptides 23 (2): 349–58. doi:10.1016/S0196-9781(01)00611-8. PMID 11825649.
- Naruse S, Kitagawa M, Ishiguro H, Hayakawa T (2002). "Feedback regulation of pancreatic secretion by peptide YY". Peptides 23 (2): 359–65. doi:10.1016/S0196-9781(01)00612-X. PMID 11825650.
- Aponte GW (2002). "PYY-mediated fatty acid induced intestinal differentiation". Peptides 23 (2): 367–76. doi:10.1016/S0196-9781(01)00613-1. PMID 11825651.
- Hagan MM (2002). "Peptide YY: a key mediator of orexigenic behavior". Peptides 23 (2): 377–82. doi:10.1016/S0196-9781(01)00614-3. PMID 11825652.
- Mannon PJ (2002). "Peptide YY as a growth factor for intestinal epithelium". Peptides 23 (2): 383–8. doi:10.1016/S0196-9781(01)00615-5. PMID 11825653.
- Tseng WW, Liu CD (2002). "Peptide YY and cancer: current findings and potential clinical applications". Peptides 23 (2): 389–95. doi:10.1016/S0196-9781(01)00616-7. PMID 11825654.
- El-Salhy M, Suhr O, Danielsson A (2002). "Peptide YY in gastrointestinal disorders". Peptides 23 (2): 397–402. doi:10.1016/S0196-9781(01)00617-9. PMID 11825655.
- Imamura M (2002). "Effects of surgical manipulation of the intestine on peptide YY and its physiology". Peptides 23 (2): 403–7. doi:10.1016/S0196-9781(01)00618-0. PMID 11825656.
- Beglinger C, Degen L (2007). "Gastrointestinal satiety signals in humans--physiologic roles for GLP-1 and PYY?". Physiol. Behav. 89 (4): 460–4. doi:10.1016/j.physbeh.2006.05.048. PMID 16828127.
- Eberlein GA, Eysselein VE, Schaeffer M, Layer P, Grandt D, Goebell H, Niebel W, Davis M, Lee TD, Shively JE, et al. (1989). "A new molecular form of PYY: structural characterization of human PYY(3-36) and PYY(1-36)". Peptides 10 (4): 797–803. doi:10.1016/0196-9781(89)90116-2. PMID 2587421.
- Facer P, Bishop AE, Cole GA, Aitchison M, Kendall CH, van Aswegen G, Penketh RJ, Rodek CH, McKeever P, Polak JM (1989). "Developmental profile of chromogranin, hormonal peptides, and 5-hydroxytryptamine in gastrointestinal endocrine cells". Gastroenterology 97 (1): 48–57. PMID 2721879.
- Tatemoto K, Nakano I, Makk G, Angwin P, Mann M, Schilling J, Go VL (1989). "Isolation and primary structure of human peptide YY". Biochem. Biophys. Res. Commun. 157 (2): 713–7. doi:10.1016/S0006-291X(88)80308-5. PMID 3202875.
- Lukinius AI, Ericsson JL, Lundqvist MK, Wilander EM (1986). "Ultrastructural localization of serotonin and polypeptide YY (PYY) in endocrine cells of the human rectum". J. Histochem. Cytochem. 34 (6): 719–26. doi:10.1177/34.6.3517149. PMID 3517149.
- Adrian TE, Ferri GL, Bacarese-Hamilton AJ, Fuessl HS, Polak JM, Bloom SR (1985). "Human distribution and release of a putative new gut hormone, peptide YY". Gastroenterology 89 (5): 1070–7. PMID 3840109.
- Lundell I, Blomqvist AG, Berglund MM, Schober DA, Johnson D, Statnick MA, Gadski RA, Gehlert DR, Larhammar D (1996). "Cloning of a human receptor of the NPY receptor family with high affinity for pancreatic polypeptide and peptide YY". J. Biol. Chem. 270 (49): 29123–8. doi:10.1074/jbc.270.49.29123. PMID 7493937.
- Bard JA, Walker MW, Branchek TA, Weinshank RL (1995). "Cloning and functional expression of a human Y4 subtype receptor for pancreatic polypeptide, neuropeptide Y, and peptide YY". J. Biol. Chem. 270 (45): 26762–5. doi:10.1074/jbc.270.45.26762. PMID 7592911.
- Hort Y, Baker E, Sutherland GR, Shine J, Herzog H (1995). "Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1". Genomics 26 (1): 77–83. doi:10.1016/0888-7543(95)80085-Z. PMID 7782089.
- Kohri K, Nata K, Yonekura H, Nagai A, Konno K, Okamoto H (1993). "Cloning and structural determination of human peptide YY cDNA and gene". Biochim. Biophys. Acta 1173 (3): 345–9. doi:10.1016/0167-4781(93)90136-2. PMID 8318545.
External links
- Peptide YY at the US National Library of Medicine Medical Subject Headings (MeSH)
PDB gallery
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1qbf: NMR SOLUTION STRUCTURE OF PORCINE PEPTIDE YY
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1ru5: Solution structure of porcine peptide YY (pPYY)
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1ruu: Solution structure of porcine peptide YY (pPYY) bound to DPC micelles
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2dez: Structure of human PYY
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2df0: Solution structure of human PYY3-36
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Hormones
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Endocrine
glands |
Hypothalamic-
pituitary
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Hypothalamus
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- GnRH
- TRH
- Dopamine
- CRH
- GHRH/Somatostatin
- Melanin concentrating hormone
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Posterior pituitary
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Anterior pituitary
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- α
- FSH
- FSHB
- LH
- LHB
- TSH
- TSHB
- CGA
- Prolactin
- POMC
- CLIP
- ACTH
- MSH
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Adrenal axis
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- Adrenal cortex
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- epinephrine
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Thyroid
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- Thyroid hormone
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- Thyroid axis
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Parathyroid
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Gonadal axis
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Testis
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Ovary
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- estradiol
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- activin and inhibin
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Placenta
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- hCG
- HPL
- estrogen
- progesterone
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Pancreas
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- glucagon
- insulin
- amylin
- somatostatin
- pancreatic polypeptide
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Pineal gland
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- melatonin
- N,N-dimethyltryptamine
- 5-methoxy-N,N-dimethyltryptamine
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Other |
Thymus
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- Thymosins
- Thymosin α1
- Beta thymosins
- Thymopoietin
- Thymulin
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Digestive system
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Stomach
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Duodenum
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- CCK
- Incretins
- secretin
- motilin
- VIP
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Ileum
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- enteroglucagon
- peptide YY
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Liver/other
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- Insulin-like growth factor
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Adipose tissue
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- leptin
- adiponectin
- resistin
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Skeleton
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Kidney
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- JGA (renin)
- peritubular cells
- calcitriol
- prostaglandin
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Heart
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Index of hormones
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Description |
- Glands
- Hormones
- thyroid
- mineralocorticoids
- Physiology
- Development
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Disease |
- Diabetes
- Congenital
- Neoplasms and cancer
- Other
- Symptoms and signs
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Treatment |
- Procedures
- Drugs
- calcium balance
- corticosteroids
- oral hypoglycemics
- pituitary and hypothalamic
- thyroid
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Neuropeptidergics
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Adiponectin |
AdipoR1
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- Agonists: Peptide: Adiponectin
- ADP-355
- ADP-399; Non-peptide: AdipoRon
- (–)-Arctigenin
- Arctiin
- Gramine
- Matairesinol
- Antagonists: Peptide: ADP-400
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AdipoR2
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- Agonists: Peptide: Adiponectin
- ADP-355
- ADP-399; Non-peptide: AdipoRon
- Deoxyschizandrin
- Parthenolide
- Syringing
- Taxifoliol
- Antagonists: Peptide: ADP-400
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CGRP |
- Agonists: Amylin
- CGRP
- Pramlintide
- Antagonists: BI 44370 TA
- BMS-927711
- CGRP (8-37)
- MK-3207
- Olcegepant
- Rimegepant
- SB-268262
- Telcagepant
- Ubrogepant
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Cholecystokinin |
CCKA
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- Agonists: Cholecystokinin
- CCK-4
- Antagonists: Amiglumide
- Asperlicin
- Devazepide
- Dexloxiglumide
- Lintitript
- Lorglumide
- Loxiglumide
- Pranazepide
- Proglumide
- Tarazepide
- Tomoglumide
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CCKB
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- Agonists: Cholecystokinin
- CCK-4
- Gastrin
- Antagonists: CI-988 (PD-134,308)
- Itriglumide
- L-365,360
- Netazepide
- Proglumide
- Spiroglumide
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Unsorted
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- Antagonists: Nastorazepide
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CRH |
CRF1
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- Agonists: Cortagine
- Corticorelin
- Corticotropin releasing hormone
- Sauvagine
- Stressin I
- Urocortin
- Antagonists: Antalarmin
- Astressin-B
- CP-154,526
- Emicerfont
- Hypericin
- LWH-234
- NBI-27914
- Pexacerfont
- R-121,919
- TS-041
- Verucerfont
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CRF2
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- Agonists: Corticorelin
- Corticotropin releasing hormone
- Sauvagine
- Urocortin
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Galanin |
GAL1
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- Agonists: Galanin
- Galanin (1-15)
- Galanin-like peptide
- Galmic
- Galnon
- Antagonists: C7
- Dithiepine-1,1,4,4-tetroxide
- Galantide (M15)
- M32
- M35
- M40
- SCH-202596
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GAL2
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- Agonists: Galanin
- Galanin (1-15)
- Galanin (2-11)
- Galanin-like peptide
- Galmic
- Galnon
- J18
- Antagonists: C7
- Galantide (M15)
- M32
- M35
- M40
- M871
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GAL3
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- Agonists: Galanin
- Galanin (1-15)
- Galmic
- Galnon
- Antagonists: C7
- Galantide (M15)
- GalR3ant
- HT-2157
- M32
- M35
- M40
- SNAP-37889
- SNAP-398299
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Ghrelin/GHS |
- Agonists: Peptide: Alexamorelin
- Cortistatin-14
- Examorelin (hexarelin)
- Ghrelin (lenomorelin)
- GHRP-1
- GHRP-3
- GHRP-4
- GHRP-5
- GHRP-6
- Ipamorelin
- Pralmorelin (GHRP-2)
- Relamorelin
- Tabimorelin
- Ulimorelin; Non-peptide: Adenosine
- Anamorelin
- Capromorelin
- CP-464709
- Ibutamoren (MK-677)
- L-692,585
- Macimorelin
- SM-130,686; Unsorted: LY-426410
- LY-444711
- Antagonists: A-778,193
- Cortistatin-8
- (D-Lys3)-GHRP-6
- JMV2959
- YIL-781
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MCH |
MCH1
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- Agonists: Melanin concentrating hormone
- Antagonists: ATC-0065
- ATC-0175
- GW-803,430
- NGD-4715
- SNAP-7941
- SNAP-94847
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MCH2
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- Agonists: Melanin concentrating hormone
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Melanocortin |
MC1
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- Agonists: α-MSH
- β-MSH
- γ-MSH
- ACTH (corticotropin)
- Afamelanotide
- BMS-470,539
- Bremelanotide
- HS-014
- HS-024
- Melanotan II
- Modimelanotide
- PL-8177
- SHU-8914
- SHU-9005
- SHU-9119
- SNAP-7941
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MC2
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- Agonists: ACTH (corticotropin)
- Alsactide
- Codactide
- Giractide
- Norleusactide (pentacosactride)
- Seractide
- Tetracosactide (tetracosactrin, cosyntropin)
- Tosactide (octacosactrin)
- Tricosactide
- Tridecactide
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MC3
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- Agonists: α-MSH
- β-MSH
- γ-MSH
- ACTH (corticotropin)
- Afamelanotide
- Bremelanotide
- Melanotan II
- Modimelanotide
- PG-931
- Antagonists: AGRP
- ASIP
- HS-014
- ML-00253764
- PG-106
- SHU-8914
- SHU-9005
- SHU-9119
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MC4
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- Agonists: α-MSH
- β-MSH
- γ-MSH
- ACTH (corticotropin)
- Afamelanotide
- AZD2820
- BIM-22493
- Bremelanotide
- LY-2112688
- Melanotan II
- MK-0493
- Modimelanotide
- PF-00446687
- PG-931
- PL-6983
- Ro 27-3225
- Setmelanotide
- THIQ
- Antagonists: AGRP
- ASIP
- HS-014
- HS-024
- HS-131
- JKC-363
- MCL-0020
- MCL-0042
- MCL-0129
- ML-00253764
- MPB-10
- SHU-8914
- SHU-9005
- SHU-9119
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MC5
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- Agonists: α-MSH
- β-MSH
- γ-MSH
- ACTH (corticotropin)
- Afamelanotide
- Bremelanotide
- HS-014
- HS-024
- Melanotan II
- Modimelanotide
- SHU-8914
- SHU-9005
- SHU-9119
- Antagonists: ASIP
- ML-00253764
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Unsorted
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- Agonists: Alsactide
- Codactide
- Giractide
- Norleusactide (pentacosactride)
- Seractide
- Tetracosactide (tetracosactrin, cosyntropin)
- Tosactide (octacosactrin)
- Tricosactide
- Tridecactide
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Neuropeptide FF |
- Agonists: Neuropeptide AF
- Neuropeptide FF
- Neuropeptide SF (RFRP-1)
- Neuropeptide VF (RFRP-3)
- Antagonists: BIBP-3226
- RF9
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Neuropeptide S |
- Antagonists: ML-154
- SHA-68
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Neuropeptide Y |
Y1
|
- Agonists: Neuropeptide Y
- Peptide YY
- Antagonists: BIBO-3304
- BIBP-3226
- BVD-10
- GR-231,118
- PD-160,170
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Y2
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- Agonists: 2-Thiouridine 5'-triphosphate
- Neuropeptide Y
- Neuropeptide Y (13-36)
- Peptide YY
- Peptide YY (3-36)
- Antagonists: BIIE-0246
- JNJ-5207787
- SF-11
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Y4
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- Agonists: GR-231,118
- Neuropeptide Y
- Pancreatic polypeptide
- Peptide YY
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Y5
|
- Agonists: BWX-46
- Neuropeptide Y
- Peptide YY
- Antagonists: CGP-71683
- FMS-586
- L-152,804
- Lu AA-33810
- MK-0557
- NTNCB
- Velneperit (S-2367)
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Neurotensin |
NTS1
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- Agonists: Neurotensin
- Neuromedin N
- Antagonists: Meclinertant
- SR-142,948
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NTS2
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- Antagonists: Levocabastine
- SR-142,948
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Opioid |
See here instead.
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Orexin |
OX1
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- Agonists: Orexin-A
- Orexin-B
- Antagonists: ACT-335827
- ACT-462206
- Almorexant
- Filorexant
- Lemborexant
- SB-334,867
- SB-408,124
- SB-649,868
- Suvorexant
- TCS-1102
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OX2
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- Agonists: Orexin-A
- Orexin-B
- SB-668,875
- Antagonists: ACT-335827
- ACT-462206
- Almorexant
- EMPA
- Filorexant
- JNJ-10397049
- MIN-202 (JNJ-42847922)
- Lemborexant
- MK-1064
- SB-649,868
- Suvorexant
- TCS-1102
- TCS-OX2-29
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Oxytocin |
- Agonists: Peptide: Aspartocin
- Carbetocin
- Cargutocin
- Demoxytocin
- Lipo-oxytocin-1
- Merotocin
- Nacartocin
- Oxytocin
- TGOT
- Vasotocin (argiprestocin); Non-peptide: TC OT 39
- WAY-267,464
- Antagonists: Peptide: Atosiban
- Tocinoic acid; Non-peptide: Barusiban
- Epelsiban
- Erlosiban
- IX-01
- L-368,899
- L-371,257
- L-372,662
- Retosiban
- SSR-126,768
- WAY-162,720
- Catabolism inhibitors: Amastatin
- Bestatin (ubenimex)
- EDTA
- L-Methionine
- Leupeptin
- o-Phenanthroline
- Phosphoramidon
- Puromycin
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Tachykinin |
NK1
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- Antagonists: Aprepitant
- Befetupitant
- Burapitant
- Casopitant
- CI-1021
- CP-96,345
- CP-99,994
- CP-122,721
- Dapitant
- Ezlopitant
- Figopitant
- FK-888
- Fosaprepitant
- Fosnetupitant
- GR-203,040
- GW-597,599
- HSP-117
- L-733,060
- L-741,671
- L-743,310
- L-758,298
- Lanepitant
- LY-306,740
- Maropitant
- Netupitant
- NKP-608
- Nolpitantium besilate
- Orvepitant
- Rolapitant
- RP-67,580
- SDZ NKT 343
- Serlopitant
- Telmapitant
- Tradipitant
- Vestipitant
- Vofopitant
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NK2
|
- Antagonists: GR-159,897
- Ibodutant
- Nepadutant
- Saredutant
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NK3
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- Antagonists: Osanetant
- Talnetant
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Vasopressin |
V1A
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- Agonists: Felypressin
- Lypressin
- Ornipressin
- Selepressin
- Terlipressin
- Vasopressin (argipressin)
- Vasotocin (argiprestocin)
- Antagonists: Atosiban
- Conivaptan
- FR-218944
- JNJ-17079166
- JNJ-17308616
- LY-307174
- PF-184563
- Relcovaptan
- RG7314
- SRX246
- SRX251
- TC OT 39
- WAY-267,464
- YM-218
- YM-471
- YM-35471
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V1B
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- Agonists: Desmopressin
- Felypressin
- Lypressin
- Ornipressin
- Terlipressin
- Vasopressin (argipressin)
- Vasotocin (argiprestocin)
- Antagonists: ABT-436
- Nelivaptan
- ORG-52186
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V2
|
- Agonists: Desmopressin
- Felypressin
- Lypressin
- Ornipressin
- TC OT 39
- Terlipressin
- Vasopressin (argipressin)
- Vasotocin (argiprestocin)
- Antagonists: Conivaptan
- JNJ-17079166
- Lixivaptan
- Mozavaptan
- RWJ-351647
- Satavaptan
- Tolvaptan
- YM-471
- YM-35471
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Unsorted
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- Antagonists: Ribuvaptan
- RWJ-339489
- VMAX-367
- VMAX-372
- VMAX-382
- YM-222546
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VIP |
VIPR1
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- Agonists: Peptide: LBT-3393
- VIP
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VIPR2
|
- Agonists: Peptide: LBT-3627
- VIP
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See also: Peptidergics
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