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Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet
Gestational protein restriction causes hypertension in the adult offspring. Very little is known about the food intake regulation and ghrelin signaling in pregnant dams fed a low-protein (LP) diet. We hypothesized that diet intake and ghrelin signaling are altered in pregnant rats fed the low-protei...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425973/ https://www.ncbi.nlm.nih.gov/pubmed/25907788 http://dx.doi.org/10.14814/phy2.12368 |
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author | Gao, Haijun Tanchico, Daren T Yallampalli, Uma Balakrishnan, Meena P Yallampalli, Chandra |
author_facet | Gao, Haijun Tanchico, Daren T Yallampalli, Uma Balakrishnan, Meena P Yallampalli, Chandra |
author_sort | Gao, Haijun |
collection | PubMed |
description | Gestational protein restriction causes hypertension in the adult offspring. Very little is known about the food intake regulation and ghrelin signaling in pregnant dams fed a low-protein (LP) diet. We hypothesized that diet intake and ghrelin signaling are altered in pregnant rats fed the low-protein diet. Sprague–Dawley rats were fed a control (CT) or LP diet from Day 3 of pregnancy. Diet intake and body weight were monitored daily. Expression of ghrelin production-related genes in the stomach and appetite-related genes in the hypothalamus was analyzed by real-time PCR. Plasma levels of total and active ghrelin, growth hormone and leptin were measured by ELISA. Main results include: (1) Daily diet intake was greater in the LP group than in the CT group in early pregnancy, but substantially lower in late pregnancy; (2) Daily gain in body weight was substantially lower in the LP group in late pregnancy; (3) Expression of ghrelin production-related genes in the stomach and plasma total ghrelin levels were increased in LP group in late pregnancy; (4) Plasma active ghrelin levels were elevated in the LP group at mid-late pregnancy, but growth hormone and leptin levels were uncorrelated with active ghrelin in late pregnancy; and (5) Hypothalamic expression of ghrelin-stimulated genes in LP rats was unassociated with the changes in both plasma ghrelin levels and the diet intake. Taken together, the appetite in LP rats is greater in early pregnancy but reduced at late pregnancy, possibly due to ghrelin insensitivity in appetite regulation. |
format | Online Article Text |
id | pubmed-4425973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44259732015-05-14 Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet Gao, Haijun Tanchico, Daren T Yallampalli, Uma Balakrishnan, Meena P Yallampalli, Chandra Physiol Rep Original Research Gestational protein restriction causes hypertension in the adult offspring. Very little is known about the food intake regulation and ghrelin signaling in pregnant dams fed a low-protein (LP) diet. We hypothesized that diet intake and ghrelin signaling are altered in pregnant rats fed the low-protein diet. Sprague–Dawley rats were fed a control (CT) or LP diet from Day 3 of pregnancy. Diet intake and body weight were monitored daily. Expression of ghrelin production-related genes in the stomach and appetite-related genes in the hypothalamus was analyzed by real-time PCR. Plasma levels of total and active ghrelin, growth hormone and leptin were measured by ELISA. Main results include: (1) Daily diet intake was greater in the LP group than in the CT group in early pregnancy, but substantially lower in late pregnancy; (2) Daily gain in body weight was substantially lower in the LP group in late pregnancy; (3) Expression of ghrelin production-related genes in the stomach and plasma total ghrelin levels were increased in LP group in late pregnancy; (4) Plasma active ghrelin levels were elevated in the LP group at mid-late pregnancy, but growth hormone and leptin levels were uncorrelated with active ghrelin in late pregnancy; and (5) Hypothalamic expression of ghrelin-stimulated genes in LP rats was unassociated with the changes in both plasma ghrelin levels and the diet intake. Taken together, the appetite in LP rats is greater in early pregnancy but reduced at late pregnancy, possibly due to ghrelin insensitivity in appetite regulation. BlackWell Publishing Ltd 2015-04-23 /pmc/articles/PMC4425973/ /pubmed/25907788 http://dx.doi.org/10.14814/phy2.12368 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Gao, Haijun Tanchico, Daren T Yallampalli, Uma Balakrishnan, Meena P Yallampalli, Chandra Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title | Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title_full | Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title_fullStr | Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title_full_unstemmed | Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title_short | Appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
title_sort | appetite regulation is independent of the changes in ghrelin levels in pregnant rats fed low-protein diet |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425973/ https://www.ncbi.nlm.nih.gov/pubmed/25907788 http://dx.doi.org/10.14814/phy2.12368 |
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