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作 者:梁永平[1] 王云满[1] 刘育军[1] 王浩[1] 付文成[1] 金周慧 彭文[1]
机构地区:[1]上海中医药大学附属普陀医院肾内科,上海200062 [2]上海利群医院肾内科,上海200085
出 处:《辽宁中医杂志》2009年第7期1218-1221,共4页Liaoning Journal of Traditional Chinese Medicine
基 金:上海市教委课题基金资助项目(07CZ015)
摘 要:目的:观察温阳活血方对慢性马兜铃酸肾病大鼠肾组织Caspase-3和BMP-7表达的影响,探讨温阳活血方对慢性马兜铃酸肾病的肾保护机制。方法:将48只雄性SD大鼠随机分为5组:(1)正常对照组(n=8):予生理盐水灌胃;(2)模型组(n=10):按关木通水煎液10mL.kg-1.d-1(相当于关木通40g.kg-1.d-1,马兜铃酸A 2.6mg.kg-1.d-1)给大鼠灌胃;(3)中药组(n=10):在模型组基础上,再予温阳活血方30g.kg-1.d-1灌胃;(4)西药组(n=10):在模型组基础上,再予科素亚33.3mg.kg-1.d-1灌胃;(5)中西药结合组(n=10):在模型组基础上,再予(温阳活血方30g.kg-1.d-1+科素亚33.3mg.kg-1.d-1)灌胃。20周末,检测大鼠尿蛋白、肾功能,光镜和电镜观察肾脏病理,采用免疫组化检测肾组织Caspase-3和BMP-7的表达。结果:与正常组和治疗组比较,模型组大鼠24h尿蛋白、Scr、BUN均明显升高(P<0.01);肾脏病理显示治疗组较模型组肾损害明显减轻;与正常对照组和治疗组比较,模型组大鼠肾组织Caspase-3表达明显升高(P<0.05),BMP-7的表达减少(P<0.01)。结论:温阳活血方能有效防治慢性马兜铃酸肾病,其机制可能与降低Caspase-3升高BMP-7有关。Objective:To explore the protective mechanism of Wen Yang Huo Xue Fang(WYI-IXF) on kidneys by investigating the effect of WYHXF on the expression of Caspase - 3 and BMP - 7 in rats with chronic aristolochic acid nephropathy. Methods : Fourty -eight male SD rats were randomly divided into five groups. Group A (n = 8 )were treated with normal saline( 10mL · kg^-1 · d^-1). Group B(n = 10)were treated with caulis Aristolochia Manshurlensis decoction( Aristolochia Manshuriensis 40g · kg^-1 · d^-1, Aristolochic acid A2. 6mg · kg^-1 · d^-1 ). Group C ( n = 10) were treated with WYHXF ( 30g · kg^-1· d ^-1 ) after the mice being modeled with the above-mentioned method. Group D( n = 10)were treated with Losartan Potassium Tablets(33.3mg · kg^-1 · d ^-1 ) after the mice being modeled with the above-mentioned method. Group E( n = 10) were treated with WYHXF( 30g · kg^-1 · d^-1)and Losartan Potassium Tablets(33.3mg · kg^-1 · d^-1) after the mice being modeled with the above-mentioned method. After 20 weeks, detection of rat urine protein, renal function, observation of renal pathology, detection of renal tissue Caspase - 3 and BMP - 7 by Immunohistochemistry. Results : Compared with those in the normal control group and the therapy group, the level of 24-hour urine protein,Scr,BUN were significantly increased in the model group( P 〈 0. 01 ) ;Renal pathology showed that the treatment group compared to the model group significantly reduce renal damage;Compared with those in the normal control group and the therapy group,the expression of Caspase- 3 was significantly increased( P 〈 0. 05), while BMP- 7 was significantly decreased in the model group (P 〈 0. 01 ). Conclusion:WYHXF exerted protective effect on CAAN probably via reduction of Caspase - 3 and elevation of BMP - 7.
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