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作 者:闵新文[1] 许明[1] 杨汉东[1] 李东峰[1]
机构地区:[1]郧阳医学院附属东风医院心内科,湖北十堰442000
出 处:《中国医师杂志》2007年第6期774-777,共4页Journal of Chinese Physician
摘 要:目的:探讨基质金属蛋白酶抑制剂-1(TIMP-1)与自发性高血压大鼠(SHR)心肌纤维化的相关性。方法:16只14周龄雄性SHR随机分为卡托普利组和SHR对照组(n=8),8只同龄雄性SD大鼠为正常对照组,卡托普利100mg·kg^-1·d^-1灌胃12周,免疫组化分析TIMP·1、CollagenⅠ和Ⅲ的表达;RT-PCR检测TIMP-1mRNA表达;MASSON染色分析测量胶原容积分数(CVF);碱水解法测定羟脯氨酸(Hypro)含量。结果:(1)SHR对照组LVI、CVF、Hypro,TIMP-1、CollagenⅠ和Ⅲ表达明显高于正常对照组(P〈0.01);相对于SHR对照组,卡托普利组则显著降低(P〈0.05);(2)TIMP-1与上述指标呈正相关(P〈0.01)。结论:TIMP-1与SHR心肌纤维化密切相关,卡托普利能抑制TIMP-1的表达。Objective To evaluate the correlation of TIMP - 1 and myocardial fibrosis in Spontaneously Hypertensive Rats. Methods 16 fourteen week old male SHRs were randomly assigned to captopril and SHR group equivalently ( n =8). 8 same age male SD rats were selected as control group. A daily dose of 100 mg · kg^-1 · d-l captopril were given for 12 weeks by gavages. TIMP - 1, Collagen Ⅰ and Ⅲ were detected by immunohistochemistry and RT - PCR. CVF was measured by MASSON staining. The concentration of Hypro was detected by alkaline hydrolysis method. Results The LVI, CVF, Hypro, and the expression of TIMP - 1, Collagen Ⅰ and Ⅲ in SHR group were significantly higher than those in SD group ( P 〈0. 01 ). Compared with the SHR group, these indices in captopril group decreased obviously ( P 〈 0. 05 ). Conclusions TIMP - 1 closely correlates with myocardial fibrosis in SHR and is suppressed by captopril.
关 键 词:金属蛋白酶1组织抑制剂 高血压 并发症 心内膜心肌纤维化症 病因学 血管肽1
分 类 号:R544[医药卫生—心血管疾病]
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