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Neuregulin 4: A “Hotline” Between Brown Fat and Liver

The discovery that functional brown adipose tissue (BAT) in adult humans is inversely related to body fat mass and may reflect metabolic health has stimulated adipose tissue research to explore activation of BAT as a potential target for antiobesity treatments. In addition to the capacity of BAT to...

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Autor principal: Blüher, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790571/
https://www.ncbi.nlm.nih.gov/pubmed/31479202
http://dx.doi.org/10.1002/oby.22595
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author Blüher, Matthias
author_facet Blüher, Matthias
author_sort Blüher, Matthias
collection PubMed
description The discovery that functional brown adipose tissue (BAT) in adult humans is inversely related to body fat mass and may reflect metabolic health has stimulated adipose tissue research to explore activation of BAT as a potential target for antiobesity treatments. In addition to the capacity of BAT to increase energy expenditure and glucose and lipid uptake, BAT secretes factors that may contribute to the regulation of whole‐body metabolism. Among signals released from BAT, neuregulin 4 (NRG4) has been recently identified as an endocrine factor that may link the activation of BAT to protection against diet‐induced obesity, insulin resistance, and hepatic steatosis. NRG4 was shown to directly reduce lipogenesis in hepatocytes, and it could indirectly activate BAT via sympathetic neurons or via inducing brown adipocyte–like signatures in white adipocytes in a paracrine manner. However, the potential relevance of NRG4 as a diagnostic tool or target for the treatment of obesity‐related diseases remains to be explored.
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spelling pubmed-67905712019-10-18 Neuregulin 4: A “Hotline” Between Brown Fat and Liver Blüher, Matthias Obesity (Silver Spring) Perspective The discovery that functional brown adipose tissue (BAT) in adult humans is inversely related to body fat mass and may reflect metabolic health has stimulated adipose tissue research to explore activation of BAT as a potential target for antiobesity treatments. In addition to the capacity of BAT to increase energy expenditure and glucose and lipid uptake, BAT secretes factors that may contribute to the regulation of whole‐body metabolism. Among signals released from BAT, neuregulin 4 (NRG4) has been recently identified as an endocrine factor that may link the activation of BAT to protection against diet‐induced obesity, insulin resistance, and hepatic steatosis. NRG4 was shown to directly reduce lipogenesis in hepatocytes, and it could indirectly activate BAT via sympathetic neurons or via inducing brown adipocyte–like signatures in white adipocytes in a paracrine manner. However, the potential relevance of NRG4 as a diagnostic tool or target for the treatment of obesity‐related diseases remains to be explored. John Wiley and Sons Inc. 2019-09-03 2019-10 /pmc/articles/PMC6790571/ /pubmed/31479202 http://dx.doi.org/10.1002/oby.22595 Text en © 2019 The Authors. Obesity published by Wiley Periodicals, Inc. on behalf of The Obesity Society (TOS) This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Perspective
Blüher, Matthias
Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title_full Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title_fullStr Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title_full_unstemmed Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title_short Neuregulin 4: A “Hotline” Between Brown Fat and Liver
title_sort neuregulin 4: a “hotline” between brown fat and liver
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790571/
https://www.ncbi.nlm.nih.gov/pubmed/31479202
http://dx.doi.org/10.1002/oby.22595
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