Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.

Interscapular brown adipose tissue (BAT) has the capability to take up glucose from the circulation. Despite the important role of BAT in the control of glucose homeostasis, the metabolic fate and function of glucose in BAT remain elusive as there is clear dissociation between glucose uptake and BAT...

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Main Authors: Eunjin Kwon, Taesik Yoo, Hye-Young Joung, Young-Hwan Jo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0228320
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spelling doaj-0ee536b686ba4f83bb48284b806385552021-06-09T04:31:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01151e022832010.1371/journal.pone.0228320Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.Eunjin KwonTaesik YooHye-Young JoungYoung-Hwan JoInterscapular brown adipose tissue (BAT) has the capability to take up glucose from the circulation. Despite the important role of BAT in the control of glucose homeostasis, the metabolic fate and function of glucose in BAT remain elusive as there is clear dissociation between glucose uptake and BAT thermogenesis. Interestingly, intracellular glycolysis and lactate production appear to be required for glucose uptake by BAT. Here, we specifically examine whether activation of lactate receptors in BAT plays a key role in regulating glucose homeostasis in mice fed a high-fat diet (HFD). When C57BL/6J mice are given HFD for 5 weeks at 28°C, male, but not female, mice gain body weight and develop hyperglycemia. Importantly, high-fat feeding upregulates expression of the lactate receptor hydroxycarboxylic acid receptor 1 (HCAR1) in female C57BL/6J mice, whereas male C57BL/6J mice show reduced HCAR1 expression in BAT. Treatment with the HCAR1 agonist lowers systemic glucose levels in male DIO mice. This reduction is associated with increased glucose uptake in BAT. Therefore, our results suggest that HCAR1 in BAT may contribute to the development of hyperglycemia in male C57BL/6J DIO mice.https://doi.org/10.1371/journal.pone.0228320
collection DOAJ
language English
format Article
sources DOAJ
author Eunjin Kwon
Taesik Yoo
Hye-Young Joung
Young-Hwan Jo
spellingShingle Eunjin Kwon
Taesik Yoo
Hye-Young Joung
Young-Hwan Jo
Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
PLoS ONE
author_facet Eunjin Kwon
Taesik Yoo
Hye-Young Joung
Young-Hwan Jo
author_sort Eunjin Kwon
title Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
title_short Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
title_full Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
title_fullStr Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
title_full_unstemmed Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.
title_sort hydrocarboxylic acid receptor 1 in bat regulates glucose uptake in mice fed a high-fat diet.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Interscapular brown adipose tissue (BAT) has the capability to take up glucose from the circulation. Despite the important role of BAT in the control of glucose homeostasis, the metabolic fate and function of glucose in BAT remain elusive as there is clear dissociation between glucose uptake and BAT thermogenesis. Interestingly, intracellular glycolysis and lactate production appear to be required for glucose uptake by BAT. Here, we specifically examine whether activation of lactate receptors in BAT plays a key role in regulating glucose homeostasis in mice fed a high-fat diet (HFD). When C57BL/6J mice are given HFD for 5 weeks at 28°C, male, but not female, mice gain body weight and develop hyperglycemia. Importantly, high-fat feeding upregulates expression of the lactate receptor hydroxycarboxylic acid receptor 1 (HCAR1) in female C57BL/6J mice, whereas male C57BL/6J mice show reduced HCAR1 expression in BAT. Treatment with the HCAR1 agonist lowers systemic glucose levels in male DIO mice. This reduction is associated with increased glucose uptake in BAT. Therefore, our results suggest that HCAR1 in BAT may contribute to the development of hyperglycemia in male C57BL/6J DIO mice.
url https://doi.org/10.1371/journal.pone.0228320
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