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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2017, Vol. 22 ›› Issue (2): 132-138.

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Protective effect of astragalosides on kidney damage in diabetic mice

LIU Xiaoyun 1, ZHANG Wen 1, LI Weiping 2, GONG Huilin 2, HAN Jia 3, LUAN Jiajie 1   

  1. 1 First Affiliated Hospital of Wannan Medical College,Wuhu 241001, Anhui, China; 2 Anhui Medical University,Hefei 230001, Anhui, China; 3 The Affiliated Hospital of Xuzhou Medical College, Xuzhou 221000, Jiangsu, China
  • Received:2016-11-22 Revised:2016-12-05 Online:2017-02-26 Published:2017-03-02

Abstract:

AIM: To study the effect of astragalosides (AST) on kidney damage and the mechanism in diabetic mice.   METHODS: The diabetic mice model was established by intraperitoneal injection with STZ and the model mice were randomly divided into model group, tempol group, AST-L group, AST-M group, and AST-H group. After 4 weeks and 6 weeks of administration, concentration of fasting blood glucose (FBG) and glycosylated serum protein (GSP) were recorded; weight and kidney indexes were calculated; renal pathological changes were observed; glomerular apoptosis and renal TGF-beta 1, Col Ⅳ mRNA expressions were detected by TUNEL and RT-PCR method, respectively. RESULTS: AST can significantly reduce the levels of serum FBG and GSP of diabetic mice induced by STZ in time and dose dependent way (P<0.01). After 6 weeks of administration, the body weight increased, while the kidney index, glomerulus defects and cell apoptosis decreased in all treatment group(P<0.01). Compared with model group, the high expression of Col Ⅳ mRNA and TGF-β1 mRNA were significantly decreased in kidney of AST 60 mg/kg dose group (P<0.05). CONCLUSION: There are some protective effects of AST on kidney of experimental diabetic mice, and its mechanism may be related to promote kidney Col Ⅳ, TGF-beta 1mRNA expression.

Key words: diabetes mellitus, astragalosides, Col Ⅳ, TGF-β1

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