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美托洛尔对大鼠冠状动脉微栓塞后心肌细胞凋亡及半胱天冬酶-9激活的影响。

Effect of metoprolol on myocardial apoptosis and caspase-9 activation after coronary microembolization in rats.

作者信息

Su Qiang, Li Lang, Liu Yang-Chun, Zhou You, Lu Yong-Guang, Wen Wei-Ming

机构信息

Department of Cardiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

Exp Clin Cardiol. 2013 Spring;18(2):161-5.

Abstract

OBJECTIVE

To explore the effect of metoprolol on myocardial apoptosis and caspase-9 activation after coronary microembolization (CME) in rats.

METHODS

Forty rats were randomly divided into four groups (n=10 each): a sham operation (control) group, CME plus saline (CME) group, CME plus metoprolol (metoprolol) group and caspase-9 inhibitor Z-LEHD-FMK (ZLF) group. CME was induced by injecting 3000 polyethylene microspheres (42 μm diameter) into the left ventricle during a 10 s occlusion of the ascending aorta. Echocardiography, terminal deoxynucleotidyl transferase dUTP nick end labelling and Western blotting were used to evaluate cardiac function, apoptosis and activation of caspase-9/caspase-3, respectively, 6 h after CME.

RESULTS

The echocardiographic parameters of left ventricular function were significantly decreased in the CME group compared with the control group (P<0.05); however, the metoprolol group and ZLF group showed significantly improved cardiac function compared with CME alone (P<0.05). Compared with the control group, the myocardial apoptosis rate and the levels of activated caspase-9 and -3 increased significantly in the CME group (P<0.05). Again, these effects were ameliorated by metoprolol and ZLF (P<0.05).

CONCLUSIONS

The present study demonstrates that metoprolol and ZLF can protect the rat myocardium during CME by inhibiting apoptosis and improving cardiac function, likely by inhibiting apoptosis/ mitochondrial apoptotic pathway. These results suggest that antiapoptotic therapies may be useful in treating CME.

摘要

目的

探讨美托洛尔对大鼠冠状动脉微栓塞(CME)后心肌细胞凋亡及半胱天冬酶-9激活的影响。

方法

40只大鼠随机分为四组(每组n = 10):假手术(对照)组、CME加生理盐水(CME)组、CME加美托洛尔(美托洛尔)组和半胱天冬酶-9抑制剂Z-LEHD-FMK(ZLF)组。在升主动脉阻断10秒期间,向左心室注射3000个聚乙烯微球(直径42μm)诱导CME。CME后6小时,分别采用超声心动图、末端脱氧核苷酸转移酶dUTP缺口末端标记法和蛋白质免疫印迹法评估心脏功能、细胞凋亡以及半胱天冬酶-9/半胱天冬酶-3的激活情况。

结果

与对照组相比,CME组左心室功能的超声心动图参数显著降低(P < 0.05);然而,与单纯CME组相比,美托洛尔组和ZLF组的心脏功能显著改善(P < 0.05)。与对照组相比,CME组心肌细胞凋亡率以及激活的半胱天冬酶-9和-3水平显著升高(P < 0.05)。同样,美托洛尔和ZLF改善了这些作用(P < 0.05)。

结论

本研究表明,美托洛尔和ZLF可通过抑制细胞凋亡和改善心脏功能来保护CME期间的大鼠心肌,可能是通过抑制细胞凋亡/线粒体凋亡途径实现的。这些结果表明,抗凋亡疗法可能对治疗CME有用。

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