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机构地区:[1]内蒙古包头医学院第二附属医院心内科,014030
出 处:《临床心血管病杂志》2010年第10期784-786,共3页Journal of Clinical Cardiology
摘 要:目的:探讨基质金属蛋白酶-2、9(MMP-2、9)在双肾一夹型高血压大鼠血管重塑中的表达及其调节机制。方法:将雄性Wistar大鼠随机分成3组,假手术(对照)组,双肾一夹型(模型)组,替米沙坦组,均在术后每周监测血压,8周后处死大鼠取胸主动脉与颈总动脉作形态学观察,免疫组化法检测MMP-2、9的蛋白表达。结果:与对照组相比,模型组血压明显升高,血管中膜增厚,MMP-2、9表达显著增加。治疗8周后,替米沙坦组血压明显降低,管壁变薄,MMP-2、9表达减少。结论:MMP-2、9可能与高血压血管重塑有关,替米沙坦通过抑制血管中MMP-2,9的表达,改善血管重塑。Objective:To explore the expression and mechanisms of MMP-2,9 on vascular remodeling of twokidney one-cliped(2KIC)hypertensive rat.Method:Male Wistar rats were randomly divided into sham operation group(n=10),2KIC model group(n=10)and telmisartan group(n=7).The blood pressure was determined every week.The morphologic changes of carotid artery and thoracic aorta were observed with HE staining after 8 weeks.Arteries was performed to valuate the expression of MMP-2,9 with mmunohistochemisty.Result:The blood pressure,vessel wall,and the expression of MMP-2,9 in model group were significantly increased compased with those of control group.After treatment with telmisartan,all of them were decreased.Conclusion: MMP-2 and 9 are related to vascular remodeling in 2KIC hypertensive rat and telmisartan could regulate vascular remodeling by inhibiting the expression of MMP-2and 9.
关 键 词:高血压 基质金属蛋白酶 双肾一夹型高血压 血管重塑 替米沙坦
分 类 号:R544.1[医药卫生—心血管疾病]
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