4.7 Article

Puerarin improves insulin resistance and modulates adipokine expression in rats fed a high-fat diet

期刊

EUROPEAN JOURNAL OF PHARMACOLOGY
卷 649, 期 1-3, 页码 398-402

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2010.09.054

关键词

Puerarin; High fat diet; Insulin resistance; Adipose tissue; Adipokine

资金

  1. Excellent Youth Foundation of Fujian Province [2009D016]
  2. Foundation of Xiamen PR China [3502Z20077050]

向作者/读者索取更多资源

The link between obesity and insulin resistance largely accounts for the pathogenesis of metabolic syndrome and diabetes mellitus in which adipokine expression plays a key role Puerarin a major active isoflavone extracted from the traditional Chinese medicine Radix Puerariae has been studied for its comprehensive biological actions However its effect on high-fat diet (HFD)-induced insulin resistance and adipokine expression in rat has not been well investigated In the present study male Sprague-Dawley rats were fed on a normal control diet (NCD) or HFD for 6 weeks followed by administration of puerarin (100 and 200 mg/kg) for up to 8 weeks Compared to NCD HFD feeding for 6 weeks led to increased body weight gain and impaired glucose/insulin tolerance manifested by oral glucose/intraperitoneal insulin tolerance tests in rats These exacerbations prolonged through HFD feeding but were effectively reversed by puerarin administration Enzyme-linked immunosorbent assay demonstrated that serum levels of leptin and resistin but not that of adiponectin were markedly augmented by HFD and retarded by puerarin treatment Real-time reverse transcription polymerase chain reaction results showed that in agreement with the circulating levels mRNA expression of leptin and resistin in epididymal white adipose tissue was modified by HFD and improved by puerarin in the same pattern Collectively we revealed that puerarin could improve body weight gain glucose/insulin intolerance and adipokine expression in HFD-induced insulin resistant rats indicating its potential value for treatment of metabolic syndrome (C) 2010 Elsevier BV All rights reserved

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