Switching harmful visceral fat to beneficial energy combustion improves metabolic dysfunctions

Visceral fat is considered the genuine and harmful white adipose tissue (WAT) that is associated to development of metabolic disorders, cardiovascular disease, and cancer. Here, we present a new concept to turn the harmful visceral fat into a beneficial energy consumption depot, which is beneficial...

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Veröffentlicht in:JCI INSIGHT 2017-02, Vol.2 (4), p.e89044-e89044
Hauptverfasser: Yang, Xiaoyan, Sui, Wenhai, Zhang, Meng, Dong, Mei, Lim, Sharon, Seki, Takahiro, Guo, Ziheng, Fischer, Carina, Lu, Huixia, Zhang, Cheng, Yang, Jianmin, Wang, Yangang, Cao, Caixia, Gao, Yanyan, Zhao, Xingguo, Sun, Meili, Sun, Yuping, Zhuang, Rujie, Samani, Nilesh J, Zhang, Yun, Cao, Yihai
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container_issue 4
container_start_page e89044
container_title JCI INSIGHT
container_volume 2
creator Yang, Xiaoyan
Sui, Wenhai
Zhang, Meng
Dong, Mei
Lim, Sharon
Seki, Takahiro
Guo, Ziheng
Fischer, Carina
Lu, Huixia
Zhang, Cheng
Yang, Jianmin
Zhang, Meng
Wang, Yangang
Cao, Caixia
Gao, Yanyan
Zhao, Xingguo
Sun, Meili
Sun, Yuping
Zhuang, Rujie
Samani, Nilesh J
Zhang, Yun
Cao, Yihai
description Visceral fat is considered the genuine and harmful white adipose tissue (WAT) that is associated to development of metabolic disorders, cardiovascular disease, and cancer. Here, we present a new concept to turn the harmful visceral fat into a beneficial energy consumption depot, which is beneficial for improvement of metabolic dysfunctions in obese mice. We show that low temperature-dependent browning of visceral fat caused decreased adipose weight, total body weight, and body mass index, despite increased food intake. In high-fat diet-fed mice, low temperature exposure improved browning of visceral fat, global metabolism via nonshivering thermogenesis, insulin sensitivity, and hepatic steatosis. Genome-wide expression profiling showed upregulation of WAT browning-related genes including and . Conversely, was unchanged in healthy mice or was downregulated in obese mice. Surgical removal of visceral fat and genetic knockdown of UCP1 in epididymal fat largely ablated low temperature-increased global thermogenesis and resulted in the death of most mice. Thus, browning of visceral fat may be a compensatory heating mechanism that could provide a novel therapeutic strategy for treating visceral fat-associated obesity and diabetes.
doi_str_mv 10.1172/jci.insight.89044
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subjects Adiponectin - metabolism
Adipose Tissue - metabolism
Adipose Tissue - pathology
Adipose Tissue, Brown - metabolism
Adipose Tissue, White - metabolism
Animals
Apoptosis Regulatory Proteins - genetics
Body Temperature
Body Weight
Cold Temperature
Diet, High-Fat
DNA-Binding Proteins - genetics
Eating
Energy Metabolism
Fatty Liver
Gene Knockdown Techniques
Insulin Resistance
Intra-Abdominal Fat - metabolism
Iodide Peroxidase - genetics
Iodothyronine Deiodinase Type II
Leptin - metabolism
Mice
Mice, Obese
Organ Size
Thermogenesis
Transcription Factors - genetics
Uncoupling Protein 1 - genetics
Up-Regulation
title Switching harmful visceral fat to beneficial energy combustion improves metabolic dysfunctions
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