Eichhorn E J, Heesch C M, Barnett J H, Alvarez L G, Fass S M, Grayburn P A, Hatfield B A, Marcoux L G, Malloy C R
Cardiac Catheterization Laboratory, Dallas Veterans Administration Hospital, Texas.
J Am Coll Cardiol. 1994 Nov 1;24(5):1310-20. doi: 10.1016/0735-1097(94)90114-7.
This study examined the effects of metoprolol on left ventricular performance, efficiency, neurohormonal activation and myocardial respiratory quotient in patients with dilated cardiomyopathy.
The mechanism by which beta-adrenergic blockade improves ejection fraction in patients with dilated cardiomyopathy remains an enigma. Thus, we undertook an extensive hemodynamic evaluation of this mechanism. In addition, because animal models have shown that catecholamine exposure may increase relative fatty acid utilization, we hypothesized that antagonism of sympathetic stimulation may result in increased carbohydrate utilization.
This was a randomized, double-blind, prospective trial in which 24 men with nonischemic dilated cardiomyopathy underwent cardiac catheterization before and after 3 months of therapy with metoprolol (n = 15) or placebo (n = 9) in addition to standard therapy. Pressure-volume relations were examined using a micromanometer catheter and digital ventriculography.
At baseline, the placebo-treated patients had somewhat more advanced left ventricular dysfunction. Ejection fraction and left ventricular performance improved only in the metoprolol-treated patients. Stroke and minute work increased without an increase in myocardial oxygen consumption, suggesting increased myocardial efficiency. Further increases in ejection fraction were seen between 3 and 6 months in the metoprolol group. The placebo group had a significant increase in ejection fraction only after crossover to metoprolol. A significant relation between the change in coronary sinus norepinephrine and myocardial respiratory quotient was seen, suggesting a possible effect of adrenergic deactivation on substrate utilization.
These data demonstrate that in patients with cardiomyopathy, metoprolol treatment improves myocardial performance and energetics, and favorably alters substrate utilization. Beta-adrenergic blocking agents, such as metoprolol, are hemodynamically and energetically beneficial in the treatment of myocardial failure.
本研究探讨了美托洛尔对扩张型心肌病患者左心室功能、效率、神经激素激活及心肌呼吸商的影响。
β-肾上腺素能阻滞剂改善扩张型心肌病患者射血分数的机制仍是一个谜。因此,我们对这一机制进行了广泛的血流动力学评估。此外,由于动物模型显示儿茶酚胺暴露可能增加相对脂肪酸利用,我们推测交感神经刺激的拮抗作用可能导致碳水化合物利用增加。
这是一项随机、双盲、前瞻性试验,24名非缺血性扩张型心肌病男性患者在接受美托洛尔(n = 15)或安慰剂(n = 9)治疗3个月前后,除标准治疗外,还接受了心导管检查。使用微压计导管和数字心室造影检查压力-容积关系。
基线时,安慰剂治疗的患者左心室功能障碍程度略重。仅美托洛尔治疗的患者射血分数和左心室功能得到改善。每搏功和每分功增加,而心肌氧耗未增加,提示心肌效率提高。美托洛尔组在3至6个月间射血分数进一步增加。安慰剂组仅在交叉使用美托洛尔后射血分数才有显著增加。观察到冠状窦去甲肾上腺素变化与心肌呼吸商之间存在显著关系,提示肾上腺素能失活对底物利用可能有影响。
这些数据表明,在心肌病患者中,美托洛尔治疗可改善心肌性能和能量代谢,并有利地改变底物利用。美托洛尔等β-肾上腺素能阻滞剂在治疗心力衰竭方面具有血流动力学和能量代谢方面的益处。