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阿魏酸哌嗪对糖尿病大鼠肾脏的保护作用
引用本文:王焕,付平,谢席胜,李静,马爱景,高玉春.阿魏酸哌嗪对糖尿病大鼠肾脏的保护作用[J].中国中西医结合肾病杂志,2008,9(7):582-585.
作者姓名:王焕  付平  谢席胜  李静  马爱景  高玉春
作者单位:王焕 (四川大学华西医院肾脏内科,成都,610041); 付平 (四川大学华西医院肾脏内科,成都,610041); 谢席胜 (四川大学华西医院肾脏内科,成都,610041); 李静 (四川大学华西医院肾脏内科,成都,610041); 马爱景 (四川大学华西医院肾脏内科,成都,610041); 高玉春 (四川大学华西医院肾脏内科,成都,610041);
摘    要:目的:观察阿魏酸哌嗪对糖尿病大鼠肾脏的保护作用。方法:将雄性SD大鼠32只随机分为4组:正常组、模型组、阿魏酸哌嗪治疗组、厄贝沙坦治疗组,采用STZ诱导的糖尿病大鼠模型,阿魏酸哌嗪组予阿魏酸哌嗪溶液50mg·kg-1·d^-1灌胃,厄贝沙坦组予厄贝沙坦溶液50mg·kg^-1·d^-1灌胃,正常组与模型组予以同等体积蒸馏水灌胃,连续8周。监测血糖,8周后处死各组大鼠,行24h尿蛋白定量和肾功能检查,称左肾重,行HE、PAS染色观察肾组织的病理变化,行免疫组化、实时荧光定量PCR观察转化生长因子-β(TGF-β)和纤连蛋白(FN)的表达情况。结果:阿魏酸哌嗪能显著减少糖尿病大鼠肾脏TGF-β和FN的表达,改善肾脏病理变化。结论:阿魏酸哌嗪对糖尿病大鼠肾脏具有保护作用,其作用机制可能与其降低TGF-β和FN的表达有关。

关 键 词:糖尿病肾病  阿魏酸哌嗪  转化生长因子-β  纤连蛋白

The Effect and its Mechanism of Piperazine Ferulate on STZ-induced Diabetic Nephropathy in Rats
Institution:WANG Huan , FU Ping, XIE Xisheng , et al (Department of Nephropathy, West China Hospital of Sichuan University, Chendu (610041)
Abstract:Objective:To study the effect and mechanism of Piperazine Ferulate on STZ- induced diabetic nephropathy in rats. Methods: 32 Sprague - Dawley rats were randomly divided into 4 groups, the normal group, diabetic nephropathy group, Piperazine Ferulate group and Irbesartan group. Piperazine Ferulate group was intragastricly administrated with PF 50 mg·kg^-1·d^-1 ; Irbesartan group was intragastricly administrated with losartan 50 mg·kg^-1·d^-1 ;the normal and diabetic nephropathy groups were intragastricly administrated with identical voluminal distilled water. After 8 weeks, rats from each group were executed. 24 hours urine protein, serum creatinine and the ratio of left renal weight/body weight was measured at the end of the study, renal pathological changes was evaluated and the expression of transforming growth factor - β(TGF- β) and Fibronectin(FN) were examined with immunohistochemisty; The rnRNA of TGF- β and FN were reversely transcribed and quantified by real - time PCR. Results:TGF-β and FiN expressions in Pauperizing Ferulae group and Irbesartan groups were significantly lower than those in diabetic nephropathy group ( P 〈 0.05). Piperazine Ferulate obviously reduced TGF - β expression and FN deposition in the renal tissues and improved the renal pathological changes in diabetic nephropathy rats. Conclusion: Piperazine Ferulate can evidently relieve renal damage in rats with diabetic nephropathy induced by STZ, which might be related to the down regulation of TGF- β and FN expression.
Keywords:Diabetic nephropathy Piperazine ferulate TGF- β FiN
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