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Ghrelin for cachexia
Ghrelin, a natural ligand for the growth hormone (GH)-secretagogue receptor, is primarily produced in the stomach. Administration of ghrelin stimulates food intake and GH secretion in both animals and humans. Ghrelin is the only circulating hormone known to stimulate appetite in humans. As GH is an...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060649/ https://www.ncbi.nlm.nih.gov/pubmed/21475698 http://dx.doi.org/10.1007/s13539-010-0011-5 |
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author | Akamizu, Takashi Kangawa, Kenji |
author_facet | Akamizu, Takashi Kangawa, Kenji |
author_sort | Akamizu, Takashi |
collection | PubMed |
description | Ghrelin, a natural ligand for the growth hormone (GH)-secretagogue receptor, is primarily produced in the stomach. Administration of ghrelin stimulates food intake and GH secretion in both animals and humans. Ghrelin is the only circulating hormone known to stimulate appetite in humans. As GH is an anabolic hormone, protein stores are spared at the expense of fat during conditions of caloric restriction. Ghrelin also inhibits the production of anorectic proinflammatory cytokines. Thus, ghrelin exhibits anti-cachectic actions via both GH-dependent and -independent mechanisms. Several studies are evaluating the efficacy of ghrelin in the treatment of cachexia caused by a variety of diseases, including congestive heart failure, chronic obstructive pulmonary disease, cancer, and end-stage renal disease. These studies will hopefully lead to the development of novel clinical applications for ghrelin in the future. These studies have also facilitated a better understanding of the molecular basis of the anti-catabolic effects of ghrelin. This review summarizes the recent advances in this area of research. |
format | Text |
id | pubmed-3060649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30606492011-04-05 Ghrelin for cachexia Akamizu, Takashi Kangawa, Kenji J Cachexia Sarcopenia Muscle Review Ghrelin, a natural ligand for the growth hormone (GH)-secretagogue receptor, is primarily produced in the stomach. Administration of ghrelin stimulates food intake and GH secretion in both animals and humans. Ghrelin is the only circulating hormone known to stimulate appetite in humans. As GH is an anabolic hormone, protein stores are spared at the expense of fat during conditions of caloric restriction. Ghrelin also inhibits the production of anorectic proinflammatory cytokines. Thus, ghrelin exhibits anti-cachectic actions via both GH-dependent and -independent mechanisms. Several studies are evaluating the efficacy of ghrelin in the treatment of cachexia caused by a variety of diseases, including congestive heart failure, chronic obstructive pulmonary disease, cancer, and end-stage renal disease. These studies will hopefully lead to the development of novel clinical applications for ghrelin in the future. These studies have also facilitated a better understanding of the molecular basis of the anti-catabolic effects of ghrelin. This review summarizes the recent advances in this area of research. Springer-Verlag 2010-12-17 2010-12 /pmc/articles/PMC3060649/ /pubmed/21475698 http://dx.doi.org/10.1007/s13539-010-0011-5 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Review Akamizu, Takashi Kangawa, Kenji Ghrelin for cachexia |
title | Ghrelin for cachexia |
title_full | Ghrelin for cachexia |
title_fullStr | Ghrelin for cachexia |
title_full_unstemmed | Ghrelin for cachexia |
title_short | Ghrelin for cachexia |
title_sort | ghrelin for cachexia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060649/ https://www.ncbi.nlm.nih.gov/pubmed/21475698 http://dx.doi.org/10.1007/s13539-010-0011-5 |
work_keys_str_mv | AT akamizutakashi ghrelinforcachexia AT kangawakenji ghrelinforcachexia |