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机构地区:[1]郑州大学第二附属医院心内科,郑州450014
出 处:《郑州大学学报(医学版)》2016年第3期393-396,共4页Journal of Zhengzhou University(Medical Sciences)
摘 要:目的:研究螺内酯对心肌肥厚大鼠IL-33/ST2通路中可溶性ST2(s ST2)的影响。方法:选取健康雄性SD大鼠30只,随机分为对照组(n=10)、模型组(n=10)、药物干预组(n=10)。对照组皮下注射生理盐水,模型组皮下注射异丙肾上腺素(ISO),药物干预组皮下注射ISO+螺内酯20 mg/(kg·d)灌胃,余各组用等量生理盐水灌胃。14 d后处死大鼠,测量心脏质量指数、左心室质量指数及心肌细胞直径;免疫组化法及RT-PCR法检测心肌组织中s ST2的表达。结果:模型组与药物干预组心脏质量指数、左心室质量指数及心肌细胞直径均高于对照组(P<0.05);模型组s ST2的表达高于对照组和药物干预组(P<0.05)。结论:螺内酯可能通过调节IL-33/ST2通路中s ST2的表达,抑制ISO诱导的心肌肥厚。Aim: To study the effects of spironolactone on s ST2 of IL-33/ST2 pathway in myocardial hypertrophy rats.Methods: A total of 30 healthy male SD rats were randomly allocated into control group( n = 10),model group( n = 10) and drug intervention group( n = 10). LVM/BM,HM/BM and the size of cardiomyocyte were detected. s ST2 mRNA and protein in left ventricular tissue were analyzed by RT-PCR and immunohistochemistry. Results: LVM/BM and HM/BM in the drug intervention group and model group were higher than those in control group( P〈0. 05). The expression of s ST2 in the model group was higher than that in the control group and drug intervention group( P〈0. 05). Conclusion: Spironolactone could modulate the expression of s ST2 in IL-33/ST2 pathway,and alleviate myocardial hypertrophy caused by isoproterenol.
分 类 号:R54[医药卫生—心血管疾病]
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