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Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism

The term energy metabolism comprises the entirety of chemical processes associated with uptake, conversion, storage, and breakdown of nutrients. All these must be tightly regulated in time and space to ensure metabolic homeostasis in an environment characterized by cycles such as the succession of d...

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Autores principales: Heyde, Isabel, Begemann, Kimberly, Oster, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864004/
https://www.ncbi.nlm.nih.gov/pubmed/33453099
http://dx.doi.org/10.1210/endocr/bqab009
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author Heyde, Isabel
Begemann, Kimberly
Oster, Henrik
author_facet Heyde, Isabel
Begemann, Kimberly
Oster, Henrik
author_sort Heyde, Isabel
collection PubMed
description The term energy metabolism comprises the entirety of chemical processes associated with uptake, conversion, storage, and breakdown of nutrients. All these must be tightly regulated in time and space to ensure metabolic homeostasis in an environment characterized by cycles such as the succession of day and night. Most organisms evolved endogenous circadian clocks to achieve this goal. In mammals, a ubiquitous network of cellular clocks is coordinated by a pacemaker residing in the hypothalamic suprachiasmatic nucleus. Adipocytes harbor their own circadian clocks, and large aspects of adipose physiology are regulated in a circadian manner through transcriptional regulation of clock-controlled genes. White adipose tissue (WAT) stores energy in the form of triglycerides at times of high energy levels that then serve as fuel in times of need. It also functions as an endocrine organ, releasing factors in a circadian manner to regulate food intake and energy turnover in other tissues. Brown adipose tissue (BAT) produces heat through nonshivering thermogenesis, a process also controlled by the circadian clock. We here review how WAT and BAT contribute to the circadian regulation of energy metabolism. We describe how adipose rhythms are regulated by the interplay of systemic signals and local clocks and summarize how adipose-originating circadian factors feed-back on metabolic homeostasis. The role of adipose tissue in the circadian control of metabolism becomes increasingly clear as circadian disruption leads to alterations in adipose tissue regulation, promoting obesity and its sequelae. Stabilizing adipose tissue rhythms, in turn, may help to combat disrupted energy homeostasis and obesity.
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spelling pubmed-78640042021-02-10 Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism Heyde, Isabel Begemann, Kimberly Oster, Henrik Endocrinology Mini-Reviews The term energy metabolism comprises the entirety of chemical processes associated with uptake, conversion, storage, and breakdown of nutrients. All these must be tightly regulated in time and space to ensure metabolic homeostasis in an environment characterized by cycles such as the succession of day and night. Most organisms evolved endogenous circadian clocks to achieve this goal. In mammals, a ubiquitous network of cellular clocks is coordinated by a pacemaker residing in the hypothalamic suprachiasmatic nucleus. Adipocytes harbor their own circadian clocks, and large aspects of adipose physiology are regulated in a circadian manner through transcriptional regulation of clock-controlled genes. White adipose tissue (WAT) stores energy in the form of triglycerides at times of high energy levels that then serve as fuel in times of need. It also functions as an endocrine organ, releasing factors in a circadian manner to regulate food intake and energy turnover in other tissues. Brown adipose tissue (BAT) produces heat through nonshivering thermogenesis, a process also controlled by the circadian clock. We here review how WAT and BAT contribute to the circadian regulation of energy metabolism. We describe how adipose rhythms are regulated by the interplay of systemic signals and local clocks and summarize how adipose-originating circadian factors feed-back on metabolic homeostasis. The role of adipose tissue in the circadian control of metabolism becomes increasingly clear as circadian disruption leads to alterations in adipose tissue regulation, promoting obesity and its sequelae. Stabilizing adipose tissue rhythms, in turn, may help to combat disrupted energy homeostasis and obesity. Oxford University Press 2021-01-16 /pmc/articles/PMC7864004/ /pubmed/33453099 http://dx.doi.org/10.1210/endocr/bqab009 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Mini-Reviews
Heyde, Isabel
Begemann, Kimberly
Oster, Henrik
Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title_full Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title_fullStr Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title_full_unstemmed Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title_short Contributions of White and Brown Adipose Tissues to the Circadian Regulation of Energy Metabolism
title_sort contributions of white and brown adipose tissues to the circadian regulation of energy metabolism
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864004/
https://www.ncbi.nlm.nih.gov/pubmed/33453099
http://dx.doi.org/10.1210/endocr/bqab009
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