Thyroid hormones in the regulation of brown adipose tissue thermogenesis
A normal thyroid status is crucial for body temperature homeostasis, as thyroid hormone regulates both heat loss and conservation as well as heat production in the thermogenic tissues. Brown adipose tissue (BAT) is the major site of non-shivering thermogenesis and an important target of thyroid horm...
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Bioscientifica
2021-03-01
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doaj-c670785fab4f4d5986c7f4291b898da02021-03-15T09:16:30ZengBioscientificaEndocrine Connections2049-36142049-36142021-03-01102R106R115https://doi.org/10.1530/EC-20-0562Thyroid hormones in the regulation of brown adipose tissue thermogenesisSarah Christine Sentis0Rebecca Oelkrug1Jens Mittag2Institute for Endocrinology and Diabetes, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Lübeck, GermanyInstitute for Endocrinology and Diabetes, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Lübeck, GermanyInstitute for Endocrinology and Diabetes, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Lübeck, GermanyA normal thyroid status is crucial for body temperature homeostasis, as thyroid hormone regulates both heat loss and conservation as well as heat production in the thermogenic tissues. Brown adipose tissue (BAT) is the major site of non-shivering thermogenesis and an important target of thyroid hormone action. Thyroid hormone not only regulates the tissue’s sensitivity to sympathetic stimulation by norepinephrine but also the expression of uncoupling protein 1, the key driver of BAT thermogenesis. Vice versa, sympathetic stimulation of BAT triggers the expression of deiodinase type II, an enzyme that enhances local thyroid hormone availability and signaling. This review summarizes the current knowledge on how thyroid hormone controls BAT thermogenesis, aiming to dissect the direct actions of the hormone in BAT and its indirect actions via the CNS, browning of white adipose tissue or heat loss over body surfaces. Of particular relevance is the apparent dose dependency of the observed effects, as we find that minor or moderate changes in thyroid hormone levels often have different effects as compared t o high pharmacological doses. Moreover, we conclude that the more recent findings requi re a reevaluation of older studies, as key aspects such as heat loss or central BAT activation may not have received the necessary attention during the interpretation of t hese early findings. Finally, we provide a list of what we believe are the most relevant ques tions in the field that to date are still enigmatic and require further studies.https://ec.bioscientifica.com/view/journals/ec/10/2/EC-20-0562.xmlthermogenesisbatthyroid hormone receptoruncoupling protein 1heat lossadrenergic sensitivity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sarah Christine Sentis Rebecca Oelkrug Jens Mittag |
spellingShingle |
Sarah Christine Sentis Rebecca Oelkrug Jens Mittag Thyroid hormones in the regulation of brown adipose tissue thermogenesis Endocrine Connections thermogenesis bat thyroid hormone receptor uncoupling protein 1 heat loss adrenergic sensitivity |
author_facet |
Sarah Christine Sentis Rebecca Oelkrug Jens Mittag |
author_sort |
Sarah Christine Sentis |
title |
Thyroid hormones in the regulation of brown adipose tissue thermogenesis |
title_short |
Thyroid hormones in the regulation of brown adipose tissue thermogenesis |
title_full |
Thyroid hormones in the regulation of brown adipose tissue thermogenesis |
title_fullStr |
Thyroid hormones in the regulation of brown adipose tissue thermogenesis |
title_full_unstemmed |
Thyroid hormones in the regulation of brown adipose tissue thermogenesis |
title_sort |
thyroid hormones in the regulation of brown adipose tissue thermogenesis |
publisher |
Bioscientifica |
series |
Endocrine Connections |
issn |
2049-3614 2049-3614 |
publishDate |
2021-03-01 |
description |
A normal thyroid status is crucial for body temperature homeostasis, as thyroid hormone regulates both heat loss and conservation as well as heat production in the thermogenic tissues. Brown adipose tissue (BAT) is the major site of non-shivering thermogenesis and an important target of thyroid hormone action. Thyroid hormone not only regulates the tissue’s sensitivity to sympathetic stimulation by norepinephrine but also the expression of uncoupling protein 1, the key driver of BAT thermogenesis. Vice versa, sympathetic stimulation of BAT triggers the expression of deiodinase type II, an enzyme that enhances local thyroid hormone availability and signaling. This review summarizes the current knowledge on how thyroid hormone controls BAT thermogenesis, aiming to dissect the direct actions of the hormone in BAT and its indirect actions via the CNS, browning of white adipose tissue or heat loss over body surfaces. Of particular relevance is the apparent dose dependency of the observed effects, as we find that minor or moderate changes in thyroid hormone levels often have different effects as compared t o high pharmacological doses. Moreover, we conclude that the more recent findings requi re a reevaluation of older studies, as key aspects such as heat loss or central BAT activation may not have received the necessary attention during the interpretation of t hese early findings. Finally, we provide a list of what we believe are the most relevant ques tions in the field that to date are still enigmatic and require further studies. |
topic |
thermogenesis bat thyroid hormone receptor uncoupling protein 1 heat loss adrenergic sensitivity |
url |
https://ec.bioscientifica.com/view/journals/ec/10/2/EC-20-0562.xml |
work_keys_str_mv |
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