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作 者:郑旭[1] 罗杰[1] 杨文英[1] 张晶[1] 陈仕明[1] 王瑶[1] 李光伟[1] 王泰玲[1]
机构地区:[1]中日友好医院内分泌科
出 处:《中华肾脏病杂志》1999年第2期91-95,共5页Chinese Journal of Nephrology
基 金:国家人事部项目资助
摘 要:目的探讨糖尿病(DM)和高血压大鼠肾脏一氧化氮(NO)途径与DM肾病的关系。方法将自发性高血压大鼠(SHR)制成链脲佐菌素(STZ)DM模型。设WKY、SHR和SHRDM三组。除形态学观察外,还测定各组大鼠肌酐清除率(Ccr)、24小时尿蛋白、血及肾组织NO含量、肾脏NO合成酶(NOS)活性和NOSmRNA表达水平。结果SHRDM组大鼠24小时尿蛋白定量20周时明显高于其余两组,Ccr无明显改变。血NO水平升高,肾NO含量降低。肾脏结构型NOS(cNOS)活性下降,诱导型NOS(iNOS)活性或iNOS/cNOS(i/c)比值增加。肾小球NOSmRNA表达面积扩大,入球动脉及小叶间动脉NOS基因表达明显下降。肾小球系膜增生,有形成KW结节或纤维蛋白帽的趋势,系膜区基质增多,基底膜增厚,肾小动脉壁厚腔窄。结论(1)STZSHRDM模型出现的24小时尿蛋白增加、肾小球系膜及肾小血管病变提示DM肾病的产生;(2)肾脏NO系统异常与DM肾病有关。Objective To study the relationship between nitric oxide(NO) pathway and diabetic nephropathy. Methods Rats were randomly divided into WKY,SHR and SHRDM which were treated with 75 mg/kg of streptozotocin(STZ) and maintained for 10 and 20 weeks respectively.Renal NO amount,NO synthase(NOS) activity and NOS mRNA expression were measured besides morphological observation. Results Glomerular lesions in SHRDM group involved mesangial cell proliferation trend of KW node and fibrin cap,and accumulation of mesangial matrix and thickness of glomerular membrane basement.There were still wall thickness and cavity stricture in renal resistant vasculature.In SHRDM it existed lower renal NO level and constitutive NOS (cNOS) activity than WKY(P<001) and higher inducible NOS(iNOS) activity or iNOS/cNOS(i/c) ratio than both WKY and SHR(P<005).The area of NOS gene expression in glomeruli expanded(P<005)whereas NOS mRNA expression in afferent arterioles and interlobular arteries(at 20 week)reduced markedly in SHRDM(P<001). Conclusion (1)the lesions of glomeruli and renal resistant vasculature caused by STZSHRDM model confirm development of diabetic nephropathy in this study.(2)diabetic nephropathy is associated with abnormality of renal NO pathway.
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