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机构地区:[1]苏州大学附属无锡市第四人民医院,无锡市214062
出 处:《中国药房》2010年第1期50-52,共3页China Pharmacy
摘 要:目的:观察基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶抑制因子-2(TIMP-2)和Ⅳ型胶原(Ⅳ-C)在糖尿病大鼠肾组织中的表达及厄贝沙坦干预后的影响。方法:30只♂SD大鼠随机分为3组:正常对照组(NC组)、糖尿病模型组(DM组)、糖尿病模型+厄贝沙坦(50mg·kg-1)组(DI组)。后2组腹腔注射链脲佐菌素诱导大鼠建立糖尿病模型后DI组灌胃厄贝沙坦。8周后,用免疫组化方法(SP法)和逆转录-聚合酶链反应法(RT-PCR)检测各组大鼠肾皮质MMP-2、TIMP-2及Ⅳ-C的表达。结果:与NC组比较,DM组大鼠肾小球MMP-2蛋白、mRNA的表达明显降低,TIMP-2及Ⅳ-C蛋白、mRNA明显增强(P<0.01),出现糖尿病肾病典型的病理改变。与DM组比较,DI组MMP-2蛋白、mRNA表达明显增强(P<0.01),TIMP-2和Ⅳ-C表达明显降低(P<0.01)。结论:厄贝沙坦可能通过调节MMP-2/TIMP-2的平衡,减少细胞外基质Ⅳ-C积聚而发挥对糖尿病大鼠的肾脏保护作用。OBJECTIVE: To investigate the expression of matrix metallopro teinase-2 (MMP-2), tissue inhibitor of metallo- proteinase-2 (TIMP-2) and collagen Ⅳ (Ⅳ-C) in kidney of diabetic rats and the intervention effect of irbesartan. METHODS: 30 male SD rats were randomly divided into three groups: normal control group (NC group), diabetes mellitus group (DM group) and diabetes mellitus+50 mg·kg^-1 irbesartan group (DI group). DM and DI group were injected with streptozocin intraperitoneally to reduce diabetic model. After 8 weeks the expression of MMP-2, TIMP-2 and IV-C in kidney tissure were determined by immunohistochemistry method (SP) and RT-PCR. RESULTS: Compared with NC group, DM group showed the expression of protein and mRNA of MMP-2 significantly reduced while that of TIMP-2 and IV-C increased (P〈0.01). The pathologic changes of diabetic nephropathy occurred in DM group. In D1 group the expression of protein and mRNA of MMP-2 increased significantly while that of TIMP-2 and IV-C (P〈0.01) decreased, as compared with DM group. CONCLUSION: Irbesartan may regulate the balnce of MMP-2 and TIMP-2 and weaken the accumulation of Ⅳ-C to protect kidney of rats.
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