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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2006, Vol. 11 ›› Issue (8): 883-887.

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Effects of puerarin on blood lipid and expression of aorta laminin B1 mRNA in streptozotocin-induced diabetic rats

LI Qiang-xiang, WANG Cai-yun1, OU Yu-lan2, HE Jin-lian1, ZHU Fei-yue1, ZHANG Zhuo1, ZHONG Hui-ju   

  1. Department of Endocrinology , Xiangya Hospital , Central SouthUniversity , Changsha 410008 , Hunan , China;
    1Department of Endocrinology , Loudi Municipal Central Hospital of Hunan province, Loudi 417000 , Hunan , China;
    2The First Affiuiated Hospifal , Nanhua University , Henyang 421001 , Hunan , China
  • Received:2006-04-28 Revised:2006-06-19 Online:2006-08-26 Published:2020-11-05

Abstract: AIM: To observe the effects of puerarin on blood lipid and expression of aorta laminin B1 mRNA in streptozotocin-induced diabetic rats.METHODS: Diabetic nephropathy rats were induced by intraperitoneal injection of STZ, and the experimental rats were divided into normal control group, model group, and puerarin group.During and after the treatment for 12 weeks, the general state, blood suger(BS) , triglyceride(TC) , cholesterol,low density lipoprotein(LDL-C) , high density lipoprotein(HDL-C) , glycosylated hemoglobin (HbA1c)and glycosylated low density lipoprotein(G-LDL) were detected.Aorta alteration of tissue morphology was observed by H.E staining, and the expressions of laminin B1 mRNA were determined by in situ hybridization analysis.RESULTS: Diabetes mellitus and aorta lesion occurred in the two model groups.Puerarin could improve the general state, decrease the level of triglyceride(P<0.05) ,serum cholesterol (P<0.05) , low density lipoprotein(P<0.05) , glycosylated hemoglobin(P<0.05) , and glycated low density lipoprotein(P<0.05) , and increase the level of high density lipoprotein(P<0.05).The expression of laminin B1 mRNA in the aorta were significantly inhibited by Puerarin (P<0.05).CONCLUSION: Puerarin have certain protective effects on aorta in rats.

Key words: puerarin, diabetic models, lipid, aorta, laminin B1 mRNA, gene expression

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