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Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain

Obesity is a major disease condition, in turn leading to pathological changes collectively recognized as metabolic syndrome. Recently angiotensin receptor AT(2)R has been associated negatively with body weight (BW) gain in male mice. However, the gender differences in AT(2)R and BW changes have not...

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Autores principales: Samuel, Preethi, Khan, Mohammad Azhar, Nag, Sourashish, Inagami, Tadashi, Hussain, Tahir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546084/
https://www.ncbi.nlm.nih.gov/pubmed/23341867
http://dx.doi.org/10.1371/journal.pone.0048425
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author Samuel, Preethi
Khan, Mohammad Azhar
Nag, Sourashish
Inagami, Tadashi
Hussain, Tahir
author_facet Samuel, Preethi
Khan, Mohammad Azhar
Nag, Sourashish
Inagami, Tadashi
Hussain, Tahir
author_sort Samuel, Preethi
collection PubMed
description Obesity is a major disease condition, in turn leading to pathological changes collectively recognized as metabolic syndrome. Recently angiotensin receptor AT(2)R has been associated negatively with body weight (BW) gain in male mice. However, the gender differences in AT(2)R and BW changes have not been studied. To understand the gender based role of AT(2)R involving BW changes, we fed male and female wild type (WT) and AT(2)R knock out (AT(2)KO) mice with C57BL6 background with high fat diet (HFD) for 16 weeks. The male AT(2)KO had higher HFD calorie intake (WT: 1280±80; AT(2)KO:1680±80 kcal) but gained less BW compared with the WT (WT: 13; AT(2)KO: 6 g). Contrary to the male animals, the female AT(2)KO mice with equivalent caloric intake (WT: 1424±48; AT(2)KO:1456±80 kcal) gained significantly more BW than the WT mice (WT: 9 g; AT(2)KO: 15 g). The male AT(2)KO on HFD displayed lower plasma insulin level, less impaired glucose tolerance (GT), and higher plasma T3 compared with WT males on HFD; whereas the female AT(2)KO mice on HFD showed elevated levels of plasma insulin, more impaired GT, lower plasma T3 and higher free fatty acid and hepatic triglycerides compared with WT females on HFD. Interestingly, compared with WT, AT(2)KO female mice had significantly lower estrogen, which was further reduced by HFD. These results suggest that AT(2)R in female mice via potentially regulating estrogen may have protective role against BW gain and impaired glucose tolerance and lipid metabolism.
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spelling pubmed-35460842013-01-22 Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain Samuel, Preethi Khan, Mohammad Azhar Nag, Sourashish Inagami, Tadashi Hussain, Tahir PLoS One Research Article Obesity is a major disease condition, in turn leading to pathological changes collectively recognized as metabolic syndrome. Recently angiotensin receptor AT(2)R has been associated negatively with body weight (BW) gain in male mice. However, the gender differences in AT(2)R and BW changes have not been studied. To understand the gender based role of AT(2)R involving BW changes, we fed male and female wild type (WT) and AT(2)R knock out (AT(2)KO) mice with C57BL6 background with high fat diet (HFD) for 16 weeks. The male AT(2)KO had higher HFD calorie intake (WT: 1280±80; AT(2)KO:1680±80 kcal) but gained less BW compared with the WT (WT: 13; AT(2)KO: 6 g). Contrary to the male animals, the female AT(2)KO mice with equivalent caloric intake (WT: 1424±48; AT(2)KO:1456±80 kcal) gained significantly more BW than the WT mice (WT: 9 g; AT(2)KO: 15 g). The male AT(2)KO on HFD displayed lower plasma insulin level, less impaired glucose tolerance (GT), and higher plasma T3 compared with WT males on HFD; whereas the female AT(2)KO mice on HFD showed elevated levels of plasma insulin, more impaired GT, lower plasma T3 and higher free fatty acid and hepatic triglycerides compared with WT females on HFD. Interestingly, compared with WT, AT(2)KO female mice had significantly lower estrogen, which was further reduced by HFD. These results suggest that AT(2)R in female mice via potentially regulating estrogen may have protective role against BW gain and impaired glucose tolerance and lipid metabolism. Public Library of Science 2013-01-15 /pmc/articles/PMC3546084/ /pubmed/23341867 http://dx.doi.org/10.1371/journal.pone.0048425 Text en © 2013 Samuel et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Samuel, Preethi
Khan, Mohammad Azhar
Nag, Sourashish
Inagami, Tadashi
Hussain, Tahir
Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title_full Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title_fullStr Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title_full_unstemmed Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title_short Angiotensin AT(2) Receptor Contributes towards Gender Bias in Weight Gain
title_sort angiotensin at(2) receptor contributes towards gender bias in weight gain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546084/
https://www.ncbi.nlm.nih.gov/pubmed/23341867
http://dx.doi.org/10.1371/journal.pone.0048425
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