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D-奈必洛尔和L-奈必洛尔对左心室收缩和舒张功能的影响:与D-L-奈必洛尔和阿替洛尔的比较。

Effects of D-nebivolol and L-nebivolol on left ventricular systolic and diastolic function: comparison with D-L-nebivolol and atenolol.

作者信息

Stoleru L, Wijns W, van Eyll C, Bouvy T, Van Nueten L, Pouleur H

机构信息

Department of Physiology and Pharmacology, University of Louvain, School of Medicine, Brussels, Belgium.

出版信息

J Cardiovasc Pharmacol. 1993 Aug;22(2):183-90. doi: 10.1097/00005344-199308000-00002.

Abstract

(D-L) Nebivolol is a new beta 1-selective adrenoceptor blocker which in normal individuals preserves rest and exercise hemodynamics. We assessed the effects of the enantiomers (L- and D-nebivolol) on left ventricular (LV) systolic and diastolic function and compared their effects with those of the racemic mixture. LV angiography (+Millar) was performed before and after intravenous (i.v.) infusion of either D- or L-nebivolol (1.25-2.5 mg, n = 22) in patients with ischemic heart disease and previous myocardial infarction. Neither L- nor D-nebivolol produced significant changes in heart rate (HR), peak (+) dP/dt, (dP/dt) DP40, cardiac index (CI) or ejection fraction (EF). Diastolic distensibility, evaluated from the shift of the pressure-volume data at the time of mitral valve opening, did not improve after D- or L-enantiomers administration. In contrast, both D-L-nebivolol 2.5 mg (n = 9) and atenolol 15 mg (n = 9) significantly reduced HR and peak (+) dP/dt, but in comparison to atenolol D-L nebivolol improved EF (+4% after D-L nebivolol vs. -4% after atenolol; p < 0.05 D-L nebivolol vs. atenolol) and maintained cardiac output CO, (+2% vs. -21%; p < 0.05 between groups). Moreover, unlike any of the other drugs in the study, the racemate shifted the diastolic pressure-volume data downward, suggesting improved LV distensibility. The beneficial effects of nebivolol on LV systolic and diastolic function appears to require the presence of both D- and L-enantiomers.

摘要

(D-L)奈必洛尔是一种新型的β1选择性肾上腺素能受体阻滞剂,在正常个体中可维持静息和运动时的血流动力学。我们评估了对映体(L-和D-奈必洛尔)对左心室(LV)收缩和舒张功能的影响,并将它们的作用与消旋混合物的作用进行比较。对患有缺血性心脏病和既往心肌梗死的患者静脉内(i.v.)输注D-或L-奈必洛尔(1.25 - 2.5mg,n = 22)前后进行左心室血管造影(+Millar)。L-和D-奈必洛尔均未使心率(HR)、峰值(+)dP/dt、(dP/dt)DP40、心脏指数(CI)或射血分数(EF)发生显著变化。根据二尖瓣开放时压力-容积数据的变化评估的舒张期扩张性,在给予D-或L-对映体后并未改善。相比之下,D-L-奈必洛尔2.5mg(n = 9)和阿替洛尔15mg(n = 9)均显著降低HR和峰值(+)dP/dt,但与阿替洛尔相比,D-L-奈必洛尔改善了EF(D-L-奈必洛尔后增加4%,阿替洛尔后降低4%;D-L-奈必洛尔与阿替洛尔相比,p < 0.05)并维持心输出量CO(分别为+2%和-21%;两组间p < 0.05)。此外,与研究中的任何其他药物不同,消旋体使舒张期压力-容积数据向下移动,提示左心室扩张性改善。奈必洛尔对左心室收缩和舒张功能的有益作用似乎需要D-和L-对映体同时存在。

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