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Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system
Brown adipose tissue (BAT) plays a central role in regulating energy homeostasis, and may provide novel strategies for the treatment of human obesity. BAT-mediated thermogenesis is regulated by mitochondrial uncoupling protein 1 (UCP1) in classical brown and ectopic beige adipocytes, and is controll...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682086/ https://www.ncbi.nlm.nih.gov/pubmed/26673120 http://dx.doi.org/10.1038/srep18013 |
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author | Kim, Minji Goto, Tsuyoshi Yu, Rina Uchida, Kunitoshi Tominaga, Makoto Kano, Yuriko Takahashi, Nobuyuki Kawada, Teruo |
author_facet | Kim, Minji Goto, Tsuyoshi Yu, Rina Uchida, Kunitoshi Tominaga, Makoto Kano, Yuriko Takahashi, Nobuyuki Kawada, Teruo |
author_sort | Kim, Minji |
collection | PubMed |
description | Brown adipose tissue (BAT) plays a central role in regulating energy homeostasis, and may provide novel strategies for the treatment of human obesity. BAT-mediated thermogenesis is regulated by mitochondrial uncoupling protein 1 (UCP1) in classical brown and ectopic beige adipocytes, and is controlled by sympathetic nervous system (SNS). Previous work indicated that fish oil intake reduces fat accumulation and induces UCP1 expression in BAT; however, the detailed mechanism of this effect remains unclear. In this study, we investigated the effect of fish oil on energy expenditure and the SNS. Fish oil intake increased oxygen consumption and rectal temperature, with concomitant upregulation of UCP1 and the β3 adrenergic receptor (β3AR), two markers of beige adipocytes, in the interscapular BAT and inguinal white adipose tissue (WAT). Additionally, fish oil intake increased the elimination of urinary catecholamines and the noradrenaline (NA) turnover rate in interscapular BAT and inguinal WAT. Furthermore, the effects of fish oil on SNS-mediated energy expenditure were abolished in transient receptor potential vanilloid 1 (TRPV1) knockout mice. In conclusion, fish oil intake can induce UCP1 expression in classical brown and beige adipocytes via the SNS, thereby attenuating fat accumulation and ameliorating lipid metabolism. |
format | Online Article Text |
id | pubmed-4682086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46820862015-12-18 Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system Kim, Minji Goto, Tsuyoshi Yu, Rina Uchida, Kunitoshi Tominaga, Makoto Kano, Yuriko Takahashi, Nobuyuki Kawada, Teruo Sci Rep Article Brown adipose tissue (BAT) plays a central role in regulating energy homeostasis, and may provide novel strategies for the treatment of human obesity. BAT-mediated thermogenesis is regulated by mitochondrial uncoupling protein 1 (UCP1) in classical brown and ectopic beige adipocytes, and is controlled by sympathetic nervous system (SNS). Previous work indicated that fish oil intake reduces fat accumulation and induces UCP1 expression in BAT; however, the detailed mechanism of this effect remains unclear. In this study, we investigated the effect of fish oil on energy expenditure and the SNS. Fish oil intake increased oxygen consumption and rectal temperature, with concomitant upregulation of UCP1 and the β3 adrenergic receptor (β3AR), two markers of beige adipocytes, in the interscapular BAT and inguinal white adipose tissue (WAT). Additionally, fish oil intake increased the elimination of urinary catecholamines and the noradrenaline (NA) turnover rate in interscapular BAT and inguinal WAT. Furthermore, the effects of fish oil on SNS-mediated energy expenditure were abolished in transient receptor potential vanilloid 1 (TRPV1) knockout mice. In conclusion, fish oil intake can induce UCP1 expression in classical brown and beige adipocytes via the SNS, thereby attenuating fat accumulation and ameliorating lipid metabolism. Nature Publishing Group 2015-12-17 /pmc/articles/PMC4682086/ /pubmed/26673120 http://dx.doi.org/10.1038/srep18013 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kim, Minji Goto, Tsuyoshi Yu, Rina Uchida, Kunitoshi Tominaga, Makoto Kano, Yuriko Takahashi, Nobuyuki Kawada, Teruo Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title | Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title_full | Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title_fullStr | Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title_full_unstemmed | Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title_short | Fish oil intake induces UCP1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
title_sort | fish oil intake induces ucp1 upregulation in brown and white adipose tissue via the sympathetic nervous system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682086/ https://www.ncbi.nlm.nih.gov/pubmed/26673120 http://dx.doi.org/10.1038/srep18013 |
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