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作 者:刘晓云[1] 张文[1] 李卫平[2] 公惠玲[2] 韩佳[3] 栾家杰[1]
机构地区:[1]皖南医学院第一附属医院药剂科 [2]安徽医科大学基础医学院 [3]徐州医学院附属医院药学部
出 处:《中国临床药理学与治疗学》2017年第2期132-138,共7页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:国家自然科学基金项目(81173624);安徽省自然科学基金项目(11040606M201);安徽省国际科技合作项目(12030603007)
摘 要:目的:研究黄芪总苷(AST)对糖尿病小鼠肾脏的保护作用及其可能的作用机制。方法:链脲佐菌素(STZ)诱导建立糖尿病小鼠模型。随机分为模型组、4-羟基-2,2,6,6-四甲基哌啶组,AST低、中、高三个剂量组。五组动物分别在给药后4周、6周,检测空腹血糖浓度(FBG)及糖化血清蛋白含量(GSP),称量体质量,计算肾脏指数,观察肾脏病理改变,TUNEL法检测肾小球细胞凋亡,RT-PCR法检测肾脏转化生长因子-β_1(TGF-β_1)、IV型胶原蛋白(Col IV)mRNA表达情况。结果:AST能显著降低STZ诱导的糖尿病小鼠FBG、GSP,且呈现时间、剂量依赖性(P<0.01)。给药后6周,各用药组小鼠体质量上升,肾脏指数下降,肾小球PAS阳性分值下降,肾小球细胞凋亡率降低(P<0.01)。与模型组比较,AST中剂量组小鼠肾脏ColⅣ、TGF-β_1mRNA表达水平明显下降(P<0.05)。结论:AST对糖尿病小鼠有肾脏保护作用,其机制可能与其促进肾脏ColⅣ、TGF-β1mRNA表达有关。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 IⅣ 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 1 mRNA expression.
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