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Neuropeptide W
Neuropeptide W (NPW), which was first isolated from the porcine hypothalamus, exists in two forms, consisting of 23 (NPW23) or 30 (NPW30) amino acids. These neuropeptides bind to one of two NPW receptors, either NPBWR1 (otherwise known as GPR7) or NPBWR2 (GPR8), which belong to the G protein-coupled...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527818/ https://www.ncbi.nlm.nih.gov/pubmed/23267349 http://dx.doi.org/10.3389/fendo.2012.00171 |
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author | Takenoya, Fumiko Kageyama, Haruaki Hirako, Satoshi Ota, Eiji Wada, Nobuhiro Ryushi, Tomoo Shioda, Seiji |
author_facet | Takenoya, Fumiko Kageyama, Haruaki Hirako, Satoshi Ota, Eiji Wada, Nobuhiro Ryushi, Tomoo Shioda, Seiji |
author_sort | Takenoya, Fumiko |
collection | PubMed |
description | Neuropeptide W (NPW), which was first isolated from the porcine hypothalamus, exists in two forms, consisting of 23 (NPW23) or 30 (NPW30) amino acids. These neuropeptides bind to one of two NPW receptors, either NPBWR1 (otherwise known as GPR7) or NPBWR2 (GPR8), which belong to the G protein-coupled receptor family. GPR7 is expressed in the brain and peripheral organs of both humans and rodents, whereas GPR8 is not found in rodents. GPR7 mRNA in rodents is widely expressed in several hypothalamic regions, including the paraventricular, supraoptic, ventromedial, dorsomedial, suprachiasmatic, and arcuate nuclei. These observations suggest that GPR7 plays a crucial role in the modulation of neuroendocrine function. The intracerebroventricular infusion of NPW has been shown to suppress food intake and body weight and to increase both heat production and body temperature, suggesting that NPW functions as an endogenous catabolic signaling molecule. Here we summarize our current understanding of the distribution and function of NPW in the brain. |
format | Online Article Text |
id | pubmed-3527818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35278182012-12-24 Neuropeptide W Takenoya, Fumiko Kageyama, Haruaki Hirako, Satoshi Ota, Eiji Wada, Nobuhiro Ryushi, Tomoo Shioda, Seiji Front Endocrinol (Lausanne) Endocrinology Neuropeptide W (NPW), which was first isolated from the porcine hypothalamus, exists in two forms, consisting of 23 (NPW23) or 30 (NPW30) amino acids. These neuropeptides bind to one of two NPW receptors, either NPBWR1 (otherwise known as GPR7) or NPBWR2 (GPR8), which belong to the G protein-coupled receptor family. GPR7 is expressed in the brain and peripheral organs of both humans and rodents, whereas GPR8 is not found in rodents. GPR7 mRNA in rodents is widely expressed in several hypothalamic regions, including the paraventricular, supraoptic, ventromedial, dorsomedial, suprachiasmatic, and arcuate nuclei. These observations suggest that GPR7 plays a crucial role in the modulation of neuroendocrine function. The intracerebroventricular infusion of NPW has been shown to suppress food intake and body weight and to increase both heat production and body temperature, suggesting that NPW functions as an endogenous catabolic signaling molecule. Here we summarize our current understanding of the distribution and function of NPW in the brain. Frontiers Media S.A. 2012-12-21 /pmc/articles/PMC3527818/ /pubmed/23267349 http://dx.doi.org/10.3389/fendo.2012.00171 Text en Copyright © 2012 Takenoya, Kageyama, Hirako, Ota, Wada, Ryushi and Shioda. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Endocrinology Takenoya, Fumiko Kageyama, Haruaki Hirako, Satoshi Ota, Eiji Wada, Nobuhiro Ryushi, Tomoo Shioda, Seiji Neuropeptide W |
title | Neuropeptide W |
title_full | Neuropeptide W |
title_fullStr | Neuropeptide W |
title_full_unstemmed | Neuropeptide W |
title_short | Neuropeptide W |
title_sort | neuropeptide w |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527818/ https://www.ncbi.nlm.nih.gov/pubmed/23267349 http://dx.doi.org/10.3389/fendo.2012.00171 |
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