Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.

With rapid economic development, the prevalence of obesity has increased remarkably worldwide. Obesity can induce a variety of metabolic diseases, such as atherosclerosis, diabetes, hypertension and coronary heart disease, which significantly endanger the health and welfare of individuals. Brown and...

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Main Authors: Haoyu Li, Chuanhai Zhang, Junyu Liu, Wenya Xie, Wentao Xu, Fei Liang, Kunlun Huang, Xiaoyun He
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0220310
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spelling doaj-d37badd20a8140a9a4ea76024c403c722021-03-03T20:33:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01147e022031010.1371/journal.pone.0220310Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.Haoyu LiChuanhai ZhangJunyu LiuWenya XieWentao XuFei LiangKunlun HuangXiaoyun HeWith rapid economic development, the prevalence of obesity has increased remarkably worldwide. Obesity can induce a variety of metabolic diseases, such as atherosclerosis, diabetes, hypertension and coronary heart disease, which significantly endanger the health and welfare of individuals. Brown and beige fat tissues play an important role in thermogenesis in mammals. Recent studies have shown that follistatin (FST) can potentially induce the browning of white adipose tissue (WAT). In this study, high-fat diet-induced obese mice were injected with follistatin for one week to explore the effects of follistatin on browning and metabolism and to determine the mechanism. The results showed that follistatin suppressed obesity caused by a high-fat diet and increased insulin sensitivity, energy expenditure, and subcutaneous fat browning. The beneficial effects remained even after a period of withdrawal. Follistatin promoted secretion of irisin from subcutaneous fat via the AMPK-PGC1α-irisin signal pathway, which induces browning of WAT, and activated the insulin pathway in beige fat thereby promoting metabolism.https://doi.org/10.1371/journal.pone.0220310
collection DOAJ
language English
format Article
sources DOAJ
author Haoyu Li
Chuanhai Zhang
Junyu Liu
Wenya Xie
Wentao Xu
Fei Liang
Kunlun Huang
Xiaoyun He
spellingShingle Haoyu Li
Chuanhai Zhang
Junyu Liu
Wenya Xie
Wentao Xu
Fei Liang
Kunlun Huang
Xiaoyun He
Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
PLoS ONE
author_facet Haoyu Li
Chuanhai Zhang
Junyu Liu
Wenya Xie
Wentao Xu
Fei Liang
Kunlun Huang
Xiaoyun He
author_sort Haoyu Li
title Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
title_short Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
title_full Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
title_fullStr Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
title_full_unstemmed Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
title_sort intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description With rapid economic development, the prevalence of obesity has increased remarkably worldwide. Obesity can induce a variety of metabolic diseases, such as atherosclerosis, diabetes, hypertension and coronary heart disease, which significantly endanger the health and welfare of individuals. Brown and beige fat tissues play an important role in thermogenesis in mammals. Recent studies have shown that follistatin (FST) can potentially induce the browning of white adipose tissue (WAT). In this study, high-fat diet-induced obese mice were injected with follistatin for one week to explore the effects of follistatin on browning and metabolism and to determine the mechanism. The results showed that follistatin suppressed obesity caused by a high-fat diet and increased insulin sensitivity, energy expenditure, and subcutaneous fat browning. The beneficial effects remained even after a period of withdrawal. Follistatin promoted secretion of irisin from subcutaneous fat via the AMPK-PGC1α-irisin signal pathway, which induces browning of WAT, and activated the insulin pathway in beige fat thereby promoting metabolism.
url https://doi.org/10.1371/journal.pone.0220310
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