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茵陈提取物对糖尿病大鼠肾组织中PTEN蛋白表达的影响及其肾脏保护作用
引用本文:张淑霞,霍文博,苏莹,李禛,田静,王彩霞,孙成博,邹颖刚,于晓艳.茵陈提取物对糖尿病大鼠肾组织中PTEN蛋白表达的影响及其肾脏保护作用[J].吉林大学学报(医学版),2019,45(4):779-783.
作者姓名:张淑霞  霍文博  苏莹  李禛  田静  王彩霞  孙成博  邹颖刚  于晓艳
作者单位:吉林大学药学院实验药理与毒理学教研室,吉林长春,130021;吉林大学第二医院妇产科,吉林长春,130041
基金项目:吉林省科技厅科技发展计划项目资助课题(20180414026GH);吉林省教育厅"十三五"科学技术项目资助课题(JJKH20180243KJ);吉林大学大学生创新创业训练计划项目资助课题(2018B2813)
摘    要:目的:探讨茵陈提取物(HACE)对糖尿病大鼠肾组织中第10号染色体缺失的磷酸酶及张力蛋白同源基因(PTEN)表达的影响,阐明HACE对糖尿病大鼠肾脏保护作用的药理学机制。方法:采用链脲佐菌素(STZ)制备糖尿病大鼠模型。30只Wistar大鼠随机分为对照组(6只)、模型组(12只)和HACE组(12只),HACE组大鼠每天1次灌胃给予HACE(5 g·kg-1),对照组和模型组大鼠每天1次灌胃给予等量生理盐水。给药4个月后检测各组大鼠尿白蛋白排泄率和尿总蛋白排泄率,HE染色观察大鼠肾组织病理形态表现,PAS和Masson染色检测肾小球细胞外基质(ECM)分布情况,免疫组织化学染色法检测大鼠肾组织中PTEN蛋白表达分布情况,Western blotting法检测各组大鼠肾脏组织中PTEN蛋白表达水平。结果:与模型组比较,HACE组大鼠肾小球系膜区扩大、PAS及Masson阳性染色物质聚集和基底膜增厚等现象明显减轻,24h尿白蛋白排泄率明显降低(P<0.05),尿总蛋白排泄率差异无统计学意义(P>0.05)。免疫组织化学染色检测,对照组大鼠肾组织PTEN蛋白表达量较高,模型组大鼠肾组织中PTEN蛋白表达量降低,HACE组大鼠肾组织中PTEN蛋白表达量趋向正常。Western blotting法检测,与对照组比较,模型组大鼠肾皮质中PTEN蛋白表达水平明显降低(P<0.05);与模型组比较,HACE组大鼠肾皮质组织中PTEN蛋白表达水平明显升高(F=5.06,P<0.05)。结论:HACE提高大鼠肾脏组织中PTEN蛋白的表达可能是其对糖尿病大鼠肾脏保护作用机制之一。

关 键 词:茵陈提取物  糖尿病  糖尿病肾病  第10号染色体缺失的磷酸酶及张力蛋白同源基因  细胞外基质
收稿时间:2018-10-12

Effect of herba artemisiae capillaris extracts on PTEN protein expression in kidney tissue of diabetic rats and its protective effect on kidney
ZHANG Shuxia,HUO Wenbo,SU Ying,LI Zhen,TIAN Jing,WANG Caixia,SUN Chengbo,ZOU Yinggang,YU Xiaoyan.Effect of herba artemisiae capillaris extracts on PTEN protein expression in kidney tissue of diabetic rats and its protective effect on kidney[J].Journal of Jilin University: Med Ed,2019,45(4):779-783.
Authors:ZHANG Shuxia  HUO Wenbo  SU Ying  LI Zhen  TIAN Jing  WANG Caixia  SUN Chengbo  ZOU Yinggang  YU Xiaoyan
Institution:1. Department of Experimental Pharmacology and Toxicology, School of Pharmacy, Jilin University, Changchun 130021, China;2. Department of Obstetrics and Gynecology, Second Hospital, Jilin University, Changchun 130041, China
Abstract:Objective:To investigate the effect of herba artemisiae capillaris extracts (HACE) on the expression of phosphatase and tensin homologue deleted chromatosome 10 (PTEN) in the kidney tissue of the diabetic rats, and to clarify the pharmacological mechanism of protective effect of HACE on the kidney of the diabetic rats. Methods:Thirty Wistar rats were randomly divided into control group (n=6), model group (n=12) and HACE group (n=12).The rats in HACE group were intragastrically administrated with HACE(5 g·kg-1) one time every day,and the rats in control group and model group were intragastrically administrated with the same volume of normal saline.The diabetic rat models were duplicated by streptozotocin (STZ). After 4 months of administration, the urinary albumin excretion rates and urinary total protein excretion rates of the rats in various groups were detected. The pathomorphology of the kindey tissue of the rats in various groups were observed by HE staining and the distribution of renal extracellular matrix (ECM) was detected by PAS and Masson staining. The expressions of PTEN protein in kidney tissue of the rats in various groups were detected by immunohistostaining and the expression levels of PTEN protein in kidney tissue of the rats in various groups were detected by Western blotting method. Results:Compared with model group, the glomerular mesangial aggregation, positive staining of PAS as well as Masson aggregation and basement membrane thickening of the rats in HACE group were significantly reduced, and the 24 h urinary albumin excretion rate was significantly decreased (P<0.05),and the urinary total protein excretion rate had no significant difference(P>0.05).The immunohistochemistry staining results showed that the expression level of PTEN protein in kidney tissue of the rats in control group was higher, the expression level of PTEN protein in the kidney tissue of the rats in model group was decreased, and the expression level of PTEN protein in kidney tissue of the rats in HACE group was increased to normal. The Western blotting results showed that the expression level of PTEN protein in the renal cortex tissue tissue of the rats in model group was significantly decreased compared with control group (P<0.05); compared with model group, the expression level of PTEN protein in renal cortex tissue of the rats in HACE group was significantly increased (P<0.05). Conclusion:HACE can increase the expression of PTEN protein in kidney tissue of the rats, which may be one of the mechanisms of its protective effect on the kidney in the diabetic rats.
Keywords:herba artemisiae capillaris extracts  diabetes mellitus  diabetic nephropathy  phosphatase and tensin homologue deleted chromatosome 10  extracellular matrix  
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