4.7 Article

Switching harmful visceral fat to beneficial energy combustion improves metabolic dysfunctions

Journal

JCI INSIGHT
Volume 2, Issue 4, Pages -

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/jci.insight.89044

Keywords

-

Funding

  1. Swedish Research Council
  2. Swedish Cancer Foundation
  3. Karolinska Institutet Foundation
  4. Karolinska Institutet distinguished professor award
  5. Torsten Soderbergs foundation
  6. European Research Council (ERC) advanced grant ANGIOFAT [250021]
  7. NOVO Nordisk Foundation
  8. NOVO Nordisk-advanced grant
  9. Royal Alice Wallenberg foundation
  10. Program of Introducing Talents of Discipline to Universities [B07035]
  11. State Program of National Natural Science Foundation of China for Innovative Research Group [81321061]
  12. State Key Program of National Natural Science of China [61331001, 81530014]
  13. International Collaboration and Exchange Program of China [81320108004]
  14. key research and development plan of Shandong Province [2015GGE27109]
  15. National Natural Science Foundation of China [81270403, 81400330, 81425004, 91339109, 81270350, 31400771, 81300234]
  16. Shandong Province Science Foundation [2014ZRE27460]
  17. Taishan Scholars Program of Shandong Province, China
  18. Novo Nordisk Fonden [NNF14OC0012835, NNF13OC0005609] Funding Source: researchfish

Ask authors/readers for more resources

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 Cidea and Dio2. Conversely, Prdm16 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available