4.5 Article

Beneficial effect of baicalin on insulin sensitivity in adipocytes of diet-induced obese mice

Journal

DIABETES RESEARCH AND CLINICAL PRACTICE
Volume 139, Issue -, Pages 262-271

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.diabres.2018.03.007

Keywords

Baicalin; GLUT4; Insulin sensitivity; Adipocytes

Funding

  1. National Natural Scientific Fund of China [81673736]
  2. Natural Scientific Fund of Jiangsu [BK20171319]
  3. Qing Lan Project of Jiangsu

Ask authors/readers for more resources

Aims: Although baicalin has been shown to increase glucose uptake and insulin sensitivity in skeletal muscle of mice, there is no literature available about the effect of baicalin on insulin sensitivity in adipocytes of diet-induced obese mice. Methods: In the present study, diet-induced obese mice were given 50 mg/kg baicalin intraperitoneally (i.p.) once a day for 21 days, and 3T3-L1 cells were treated with 100, 200, 400 mu M baicalin for 3 h. Then insulin resistance indexes and insulin signal protein levels were examined to elucidate whether baicalin increased glucose uptake and GLUT4 translocation in adipocytes of diet-induced obese mice. Results: The present findings showed that administration of baicalin decreased food intake, body weight, HOMA-IR and p-p38 MAPK and pERK levels, but enhanced pAKT and PGC-1 alpha contents, as well as GLUT4 mRNA, PGC-1 alpha mRNA expression in adipocytes, and reversed high fat diet-induced glucose intolerance, hyperglycemia and insulin resistance in diet-induced obese mice. Moreover, baicalin treatment increased GLUT4 concentration in plasma membranes of adipocytes. Conclusions: These data demonstrated that baicalin accelerated GLUT4 translocation from intracellular membrane compartments to plasma membranes in adipocytes. Baicalin plays a significant role in elevation of glucose uptake and insulin sensitivity to promote glucose clearance. (C) 2018 Elsevier B.V. All rights reserved.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available