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Supervised by Ministry of Industry and Information Technology of The People's Republic of China Sponsored by Harbin Institute of Technology Editor-in-chief Yu Zhou ISSNISSN 1005-9113 CNCN 23-1378/T

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Related citation:ZHAO Ying,ZHOU You,YIN Hui-jun,ZHANG Ying.Effect of puerarin on the P13K pathway for glucose transportation and insulin signal transduction in adipocytes[J].Journal of Harbin Institute Of Technology(New Series),2009,16(1):47-50.DOI:10.11916/j.issn.1005-9113.2009.01.010.
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Effect of puerarin on the P13K pathway for glucose transportation and insulin signal transduction in adipocytes
Author NameAffiliation
ZHAO Ying Postdoctoral Station of Harbin Commercial University, Harbin 150076, China 
ZHOU You Postdoctoral Station of Harbin Commercial University, Harbin 150076, China 
YIN Hui-jun Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China 
ZHANG Ying Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China 
Abstract:
To explore the effect of puerarin on insulin receptor (IR), insulin receptor substrate-1 (IRS-1) and protein expression of protein kinase B(PKB) in the P13K pathway of the glucose consumption, transportation and insulin signal transduction in 3T3-L1 adipocytes with insulin resistance. The insulin resistance 3T3-L1 adipocytes model was established by free fatty acid induction. The model cells were managed with puerarin in different concentrations. Glucose consumption was detected with glucose oxidase method, glucose transportation rate was determined by 2-deoxy-3H glucose ingesting method, and the IR, IRS-1 and PKB expression were determined by Western blot. Glucose consumption and transportation were significantly decreased in the model adipocytes, but increased after treated with puerarin (P<0.01). Moreover, the level of tyrosine phosphorylation of IR subunit β was higher in the puerarin treated groups, and that of IRS-1 was higher in the group treated with low dose puerarin than that in the model group. The 3T3-L1 adipocytes of insulin resistance model could be induced by free fatty acid successfully, puerarin could promote the glucose utilization in them to alleviate the insulin resistance, which may be related with the action in advancing the tyrosine phosphorylation of IR and IRS-1.
Key words:  puerarin  insulin resistance  glucose transportation  insulin signal transduction
DOI:10.11916/j.issn.1005-9113.2009.01.010
Clc Number:R285
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