Clinical pharmacodynamics of nebivolol: new evidence of nitric oxide-mediated vasodilating activity and peculiar haemodynamic properties in hypertensive patients.

Alberto Zanchetti
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引用次数: 80

Abstract

New evidence from recently completed clinical studies performed with nebivolol, a highly selective beta-1 beta-blocker, endowed with additional vasodilating activity mediated by nitric oxide (NO) endothelial release, confirm previous findings that nebivolol differs from other beta-blocking agents and that the combination of beta-1 blockade and NO-mediated vasodilation not only potentiates the blood pressure lowering activity, but leads to a broader favourable haemodynamic profile, which is clinically relevant to the treatment of hypertensive patients. In particular, six new studies focusing on the vasodilation properties of nebivolol demonstrated that: (i) its blood pressure lowering effect is accompanied by a vasodilating action that is seen after single and chronic administration of the usual antihypertensive oral dose of 5 mg once daily; (ii) the vasodilation can be documented systemically, at various regional vascular beds and skin microcirculation, and is accompanied by increased small arterial distensibility; (iii) the NO-endothelium-dependency of its vasodilating action is shown by the model of forearm or cutaneous vasodilating response to acetylcholine and by the blockade of the nebivolol-induced local vasodilation by a blocker of the arginine-NO cascade, L-NMMA. Two more studies demonstrated the ability of nebivolol to increase NO concentrations through preservation of NO from oxidative degradation, and not only by stimulation of its synthesis. Finally, two studies confirmed the favourable haemodynamic action of nebivolol on both systolic and diastolic function and, in particular, an increase in stroke volume, associated with reduction in vascular resistance, resulting in a maintained cardiac output despite reduced heart rate. These properties consistently differentiate nebivolol from non-vasodilating beta-blockers, such as those used for the active comparative studies, i.e. atenolol, metoprolol or bisoprolol. The observation that nebivolol enhances or restores NO-mediated vasodilation in hypertensive patients has important therapeutic implications in view of the well-established protective role of NO against cardiovascular risk factors, and particularly the development of atherosclerosis. Similarly, the favourable haemodynamic profile of nebivolol, as described by the new investigations (preservation of cardiac output, reduction of peripheral resistance and improved diastolic function) appear to have clinically relevant benefits on the impairment in systolic and/or diastolic function often complicating the hypertension.

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奈比洛尔的临床药效学:高血压患者一氧化氮介导的血管舒张活性和特殊血流动力学特性的新证据。
最近完成的关于奈比洛尔的临床研究的新证据证实,奈比洛尔是一种高度选择性的β -1 β受体阻滞剂,具有由一氧化氮(NO)内皮释放介导的额外血管舒张活性,证实了奈比洛尔不同于其他β -受体阻滞剂的发现,β -1阻滞剂和NO介导的血管舒张的结合不仅增强了降血压活性,而且导致了更广泛的有利的血流动力学特征。这对高血压患者的治疗有临床意义。特别是,六项关于奈比洛尔血管舒张特性的新研究表明:(1)其降压作用伴随着血管舒张作用,这是在常规降压口服剂量5mg每日一次的单次和慢性给药后看到的;(ii)血管舒张可在不同区域血管床和皮肤微循环中系统性记录,并伴有小动脉扩张性增加;(iii)其血管舒张作用的no -内皮依赖性通过对乙酰胆碱的前臂或皮肤血管舒张反应模型以及通过精氨酸- no级联的阻断剂L-NMMA阻断奈比洛尔诱导的局部血管舒张来显示。另外两项研究表明,奈比洛尔不仅通过刺激一氧化氮合成,而且通过保护一氧化氮免受氧化降解而增加一氧化氮浓度。最后,两项研究证实了奈比洛尔对收缩期和舒张期功能的有利血流动力学作用,特别是与血管阻力降低相关的卒中容量增加,从而在心率降低的情况下维持心输出量。这些特性将奈比洛尔与非血管扩张受体阻滞剂(如用于活性比较研究的阿替洛尔、美托洛尔或比索洛尔)区分开来。鉴于一氧化氮对心血管危险因素的保护作用,特别是对动脉粥样硬化的发展,奈比洛尔增强或恢复一氧化氮介导的高血压患者血管舒张的观察具有重要的治疗意义。同样,新的研究表明,奈比洛尔有利的血流动力学特征(保持心输出量,降低外周阻力和改善舒张功能)似乎对高血压合并的收缩期和/或舒张期功能损害具有临床相关益处。
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