Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition

Abstract Ghrelin, a circulating orexigenic hormone secreted from the stomach, stimulates appetite and food intake by activating the hypothalamic arcuate nucleus. Administration of exogenous ghrelin exerts anabolic effects, causing weight gain, increased adiposity, and decreased metabolism. Body temp...

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Autores principales: Takahiro Sato, Kanae Oishi, Daisuke Koga, Takanori Ida, Yusuke Sakai, Kenji Kangawa, Masayasu Kojima
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3760edb0716a4432af266d328de19dbe
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spelling oai:doaj.org-article:3760edb0716a4432af266d328de19dbe2021-12-02T18:49:53ZThermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition10.1038/s41598-021-97440-y2045-2322https://doaj.org/article/3760edb0716a4432af266d328de19dbe2021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-97440-yhttps://doaj.org/toc/2045-2322Abstract Ghrelin, a circulating orexigenic hormone secreted from the stomach, stimulates appetite and food intake by activating the hypothalamic arcuate nucleus. Administration of exogenous ghrelin exerts anabolic effects, causing weight gain, increased adiposity, and decreased metabolism. Body temperature (BT), which is determined by the balance of heat production and heat loss, must be strictly regulated to maintain proper cellular function and metabolism. However, the role of ghrelin in thermoregulation remains unclear. In this study, we found that ghrelin was essential for decreasing BT when mice are placed under calorie restriction. Elevated ghrelin concentrations induced by fasting correlated with significant decreases in BT, a hibernation-like state called torpor. Ghrelin-deficient (Ghrl −/− ) animals could not enter torpor. The BT of Ghrl −/− mice also remained high under restricted feeding, but the animals gradually entered precipitous hypothermia, indicating thermoregulatory impairment. These effects of ghrelin on thermoregulation were the result of suppression of sympathetic nervous system activity input to brown adipose tissue; in the absence of ghrelin, it was not possible to suppress uncoupling protein 1 (ucp1) expression and decrease BT in low-energy states. Together, these findings demonstrate that ghrelin is an essential circulating hormone involved in lowering BT.Takahiro SatoKanae OishiDaisuke KogaTakanori IdaYusuke SakaiKenji KangawaMasayasu KojimaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Takahiro Sato
Kanae Oishi
Daisuke Koga
Takanori Ida
Yusuke Sakai
Kenji Kangawa
Masayasu Kojima
Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
description Abstract Ghrelin, a circulating orexigenic hormone secreted from the stomach, stimulates appetite and food intake by activating the hypothalamic arcuate nucleus. Administration of exogenous ghrelin exerts anabolic effects, causing weight gain, increased adiposity, and decreased metabolism. Body temperature (BT), which is determined by the balance of heat production and heat loss, must be strictly regulated to maintain proper cellular function and metabolism. However, the role of ghrelin in thermoregulation remains unclear. In this study, we found that ghrelin was essential for decreasing BT when mice are placed under calorie restriction. Elevated ghrelin concentrations induced by fasting correlated with significant decreases in BT, a hibernation-like state called torpor. Ghrelin-deficient (Ghrl −/− ) animals could not enter torpor. The BT of Ghrl −/− mice also remained high under restricted feeding, but the animals gradually entered precipitous hypothermia, indicating thermoregulatory impairment. These effects of ghrelin on thermoregulation were the result of suppression of sympathetic nervous system activity input to brown adipose tissue; in the absence of ghrelin, it was not possible to suppress uncoupling protein 1 (ucp1) expression and decrease BT in low-energy states. Together, these findings demonstrate that ghrelin is an essential circulating hormone involved in lowering BT.
format article
author Takahiro Sato
Kanae Oishi
Daisuke Koga
Takanori Ida
Yusuke Sakai
Kenji Kangawa
Masayasu Kojima
author_facet Takahiro Sato
Kanae Oishi
Daisuke Koga
Takanori Ida
Yusuke Sakai
Kenji Kangawa
Masayasu Kojima
author_sort Takahiro Sato
title Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
title_short Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
title_full Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
title_fullStr Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
title_full_unstemmed Thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
title_sort thermoregulatory role of ghrelin in the induction of torpor under a restricted feeding condition
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3760edb0716a4432af266d328de19dbe
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