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Hemodynamic characterization of left ventricular function in experimental coxsackieviral myocarditis: effects of carvedilol and metoprolol.

机译:实验性柯萨奇病毒性心肌炎左心室功能的血流动力学特征:卡维地洛和美托洛尔的影响。

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Background: Carvedilol, a vasodilating nonselective beta-adrenoceptor antagonist, but not metoprolol, a selective beta(1)-adrenoceptor antagonist, has been shown to increase the production of cardiac antiinflammatory cytokines in experimental myocarditis. However, the hemodynamic consequences of these differences had not been investigated until today. Therefore, we determined the effects of carvedilol and metoprolol on left ventricular function in a murine model of coxsackievirus B3 (CVB3)-induced myocarditis. Methods: BALB/c mice were inoculated with the coxsackie-B3 virus. Four and 10 days after infection, left ventricular function was investigated using a conductance micromanometer system. Additional groups were treated starting 24 h after infection using equipotent doses of carvedilol and metoprolol and studied on day 10. Results: On day 4, infected mice manifested increased afterload-enhanced contractility and abnormal diastolic function. On day 10, contractile function of untreated mice was impaired. Carvedilol significantly improved cardiac index and most systolic indices, whereas metoprolol was substantially less effective. Diastolic dysfunction was not influenced by either of the beta-adrenoceptor antagonists. Conclusions: These hemodynamic data indicate that not only beta(1)-adrenoceptor blockade but also pleiotropic effects are involved in the cardioprotective effects of carvedilol on the pathophysiology of acute viral myocarditis.
机译:背景:卡维地洛是一种血管扩张性的非选择性β-肾上腺素受体拮抗剂,但美托洛尔不是一种选择性β(1)-肾上腺素受体拮抗剂,已被证明能增加实验性心肌炎中心脏消炎细胞因子的产生。然而,这些差异的血液动力学后果直到今天才被研究。因此,我们确定了卡维地洛和美托洛尔对柯萨奇病毒B3(CVB3)诱发的心肌炎小鼠模型中左心室功能的影响。方法:给BALB / c小鼠接种柯萨奇-B3病毒。感染后第4天和第10天,使用电导微压计系统检查左心室功能。在感染后24小时开始,使用等量的卡维地洛和美托洛尔对其他组进行治疗,并在第10天进行研究。结果:在第4天,感染的小鼠表现出增加的后负荷增强的收缩力和异常的舒张功能。在第10天,未处理的小鼠的收缩功能受损。卡维地洛可显着改善心脏指数和大多数收缩指数,而美托洛尔的疗效明显较差。舒张功能障碍不受任何一种β-肾上腺素受体拮抗剂的影响。结论:这些血液动力学数据表明,卡维地洛对急性病毒性心肌炎的病理生理保护作用不仅涉及β(1)-肾上腺素受体阻滞,而且还涉及多效性作用。

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