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机构地区:[1]天津医科大学研究生院,300070 [2]天津市儿童医院肾内科
出 处:《中华实用儿科临床杂志》2013年第17期1323-1326,共4页Chinese Journal of Applied Clinical Pediatrics
摘 要:目的 通过观察足蛋白Ezrin和NEPH1在多柔比星肾病大鼠肾组织中的表达及泼尼松对其表达的影响,探讨蛋白尿产生的机制及泼尼松对肾脏的保护作用.方法 将24只大鼠随机分为空白对照组、模型组、泼尼松干预组,通过分次尾静脉注射法建立多柔比星肾病大鼠模型,监测第4、8周时大鼠血生化及24 h尿蛋白变化.应用免疫组织化学两步法观察肾组织中足蛋白Ezrin和NEPH1表达的变化.结果 实验第4周,与空白对照组比较,模型组与泼尼松干预组均出现大量蛋白尿、低清蛋白血症和高脂血症(P均<0.01),提示模型建立成功;实验第8周,与模型组比较,泼尼松干预组24 h尿蛋白、总胆固醇、血肌酐水平显著降低(P均<0.01),清蛋白、总蛋白、内生肌酐清除率均增高(P均<0.05);免疫组织化学示模型组Ezrin和NEPH1的表达较空白对照组显著降低(P均<0.01),泼尼松干预组Ezrin和NEPH1的表达较模型组显著增加(P均<0.01),足蛋白Ezrin、NEPH1的表达与24 h尿蛋白均呈负相关(r=-0.838、-0.884,P均<0.01).结论 足蛋白Ezrin和NEPH1表达下降可能是多柔比星肾病大鼠蛋白尿产生的机制之一.泼尼松可能通过增加Ezrin和NEPH1的表达减少尿蛋白,起到保护肾脏的作用.Objective To explore the mechanism of proteinuria and renal protection of prednisone by observing the expressions of Ezrin and NEPH1 in rats with Adriamycin (ADR)-induced nephrosis.Methods The 24 rats were divided into 3 groups,which were control group,model group and prednisone group.ADR model was induced by a tail intravenous injection of ADR for 2 times.Serum index and 24 h urinary protein were measured in 4 and 8 weeks.The expressions of Ezrin and NEPH1 in glomerulus were evaluated by using two-step immunohistochemistry respectively.Results Compared with control group,heavy proteinuria,hypoalbuminemia,hyperlipemia were observed in 4 weeks in the model group and the prednisone group which indicated that the models were successfully established.Compared with model group,in 8 weeks,24 h urinary protein,total cholesterol and serum creatinine in prednisone group were significantly decreased(all P < 0.0 l),while albumin,total protein and endogenous creatinine clearance rate were significantly increased(all P < 0.05) ;The expressions of Ezrin and NEPH1 in model group were significantly decreased compared with control group(all P < 0.01).The expressions of Ezrin and NEPH1 in prednisone group were significantly increased compared with model group(all P <0.01).The expressions of Ezrin and NEPH1 were negatively related to proteinuria(r =-0.838,-0.884,all P < 0.01).Conclusions The declined expressions of Ezrin and NEPH1 in rats with ADR-induced nephrosis may be one of mechanisms of proteinuria.Prednisone can reduce the proteinuria and relieve the renal pathological damage by improving the expression of Ezrin and NEPH1.
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