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- Title
Chronic Urotensin-II Administration Improves Whole-Body Glucose Tolerance in High-Fat Diet-Fed Mice.
- Authors
Chen, Xi; Yin, Lin; Jia, Wei-hua; Wang, Nuo-qi; Xu, Chun-yang; Hou, Bi-yu; Li, Na; Zhang, Li; Qiang, Gui-fen; Yang, Xiu-ying; Du, Guan-hua
- Abstract
Urotensin-II (U-II) is an endogenous peptide agonist of a G protein-coupled receptor—urotensin receptor. There are many conflicting findings about the effects of U-II on blood glucose. This study aims to explore the effects of U-II on glucose metabolism in high-fat diet-fed mice. Male C57BL/6J mice were fed a 45% high-fat diet or chow diet and were administered U-II intraperitoneally for in vivo study. Skeletal muscle C2C12 cells were used to determine the effects of U-II on glucose and fatty acid metabolism as well as mitochondrial respiratory function. In this study, we found that chronic U-II administration (more than 7 days) ameliorated glucose tolerance in high-fat diet-fed mice. In addition, chronic U-II administration reduced the weight gain and the adipose tissue weight, including visceral, subcutaneous, and brown adipose tissue, without a significant change in blood lipid levels. These were accompanied by the increased mRNA expression of the mitochondrial thermogenesis gene Ucp3 in skeletal muscle. Furthermore, in vitro treatment with U-II directly enhanced glucose and free fatty acid consumption in C2C12 cells with increased aerobic respiration. Taken together, chronic U-II stimulation leads to improvement on glucose tolerance in high-fat diet-fed mice and this effect maybe closely related to the reduction in adipose tissue weights and enhancement on energy substrate utilization in skeletal muscle.
- Subjects
BROWN adipose tissue; G protein coupled receptors; GLUCOSE; FREE fatty acids; BLOOD sugar
- Publication
Frontiers in Endocrinology, 2019, p1
- ISSN
1664-2392
- Publication type
Article
- DOI
10.3389/fendo.2019.00453