JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2010, Vol. 48 ›› Issue (9): 1-.

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Effect of aldosterone on PTEN expression and the PI3K-Akt pathway in 3T3-L1 adipocytes

CAO Cai-xia, LI Li, SUN Rui-xia, XIAN Yu-xin, GAO Yan-yan   

  1. Department of Endocrinology, the Affiliated Hospital of Medical College of Qingdao University, Qingdao 266003, Shandong, China
  • Received:2010-05-23 Online:2010-09-16 Published:2010-09-16

Abstract:

Objective    To investigate the effects of aldosterone  on the expression of phosphoserine 473-Akt and PTEN in normal or insulin resistant adipocytes,  with the aim to explore the role of  aldosterone in the pathogenesis of insulin resistance. Methods    Insulin resistant 3T3-L1 adipocytes were induced by dexamethasone and insulin. The protein expressions of  PTEN and phosphoserine 473-AKT in normal and insulin resistant adipocytes treated with aldosterone or  spironolactone were measured by Western blot. Results    Compared with normal adipocytes, expression of PTEN protein increased(0.83±0.11)vs(0.63±0.06), P<0.05] and phosphoserine 473-AKT protein  decreased(0.52±0.12)vs(0.78±0.12), P<0.05] in insulin resistant models. Aldosterone-induced upregulation of PTEN and degradation of phosphoserine 473AKT was markedly attenuated by spironolactone,  a mineralocorticoid receptor antagonist(all P<0.05). Conclusion    Aldosterone induces insulin resistance possibly via the PI3K-Akt pathway in 3T3-L1 adipocytes.

Key words: Aldosterone; Spironolactone; phosphatase and tensin homologue deleted on chromosome 10; Phosphatidylinositol 3-kinase-Akt; Insulin resistance

CLC Number: 

  • R589
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