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ZAG alleviates HFD-induced insulin resistance accompanied with decreased lipid depot in skeletal muscle in mice
- Source :
- Journal of Lipid Research; December 2018, Vol. 59 Issue: 12 p2277-2286, 10p
- Publication Year :
- 2018
-
Abstract
- Over the past two decades, intramuscular lipids have been viewed as a cause of insulin resistance due to their ability to suppress insulin-stimulated glucose uptake in skeletal muscle. Zinc-α2-glycoprotein (ZAG) is an adipokine involved in lipolysis of white adipose tissue (WAT). To investigate the action of ZAG on insulin resistance induced by a high-fat diet (HFD), which affects the intramuscular fat, mice were divided into three groups, normal diet, HFD, and ZAG treatment under HFD (HFZ). The results showed that the insulin sensitivity of ZAG-treated mice was significantly improved. The body weight, WAT weight, and intramuscular fat were significantly decreased in the HFZ group compared with the HFD group. The lipolytic enzymes, including phosphorylation of hormone-sensitive lipase and adipose triglyceride lipase, were significantly upregulated in the skeletal muscle of mice that received the ZAG treatment compared with the HFD group. Insulin signaling proteins, such as phosphorylation of insulin receptor substrate 1 and cell membrane glucose transporter type 4, were also significantly increased in the skeletal muscle of the ZAG-treated group. Furthermore, a metabolic rate study showed that ZAG overexpression increases the respiratory exchange ratio and heat production. In vitro, ZAG treatment promotes glucose uptake and decreases intracellular lipids in C2C12 myotubes. Taken together, these data showed that overexpression of ZAG alleviates HFD-induced insulin resistance in mice, along with decreasing the lipid content of skeletal muscle.
Details
- Language :
- English
- ISSN :
- 00222275 and 15397262
- Volume :
- 59
- Issue :
- 12
- Database :
- Supplemental Index
- Journal :
- Journal of Lipid Research
- Publication Type :
- Periodical
- Accession number :
- ejs47266076
- Full Text :
- https://doi.org/10.1194/jlr.M082180