亲脂性钙拮抗剂的药理学性质。

Blood pressure. Supplement Pub Date : 1998-01-01
P A van Zwieten
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引用次数: 0

摘要

几种类型的钙拮抗剂(CA)(维拉帕米,地尔硫卓,硝苯地平及相关药物)可用于降压药。在实践中,二氢吡啶类药物(硝苯地平及相关药物)是最常用的抗高血压药物。除了降低血压外,CA还可能导致其他理论上有益的作用:左心室消退和血管肥大、肾保护、弱利钠、弱抗血小板、抗缺血和抗动脉粥样硬化活性。近年来介绍了几种新的二氢吡啶类CA。较新的化合物,如氨氯地平、非洛地平、伊地平、拉西地平和莱卡尼地平的优点可能包括:血管选择性,因此很少或没有心脏抑制剂活性;改善的动力学特征,导致起效缓慢,作用持续时间长,较少的副作用,如反射性心动过速和头痛,由于起效缓慢的降压作用。一些较新的CA主要作用于专门的循环床(肾、冠状动脉和脑)。新的CA显然是亲脂性的,值得特别注意。由于这些化合物的亲脂性,在含脂膜库中会出现相当大的浓度。这样被浓缩的钙离子缓慢地从这些钙离子库中释放出来,随后到达它们的目标——l型钙离子通道。这一现象解释了这些CA发病缓慢和作用持续时间长的原因。由于动作发病缓慢,反射性心动过速几乎不存在。作用持续时间长,可以通过每日一次剂量的方法满意地控制高血压患者的血压。少数亲脂性二氢吡啶CA具有血管选择性。这一特性表明,在治疗性的血管扩张剂量下,没有发生心脏抑制活性。来卡尼地平是最近引进的一种亲脂性和血管选择性的二氢吡啶类CA。它是一种有效的血管扩张剂/降压药,起效慢,持续时间长,与反射性心动过速和心脏抑制活性无关。最近引入的亲脂性CA的其他例子是拉西地平,巴尼地平和曼尼地平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The pharmacological properties of lipophilic calcium antagonists.

Several types of calcium antagonists (CA) (verapamil, diltiazem, nifedipine and related drugs) may be used as antihypertensives. In practice, the dihydropyridines (nifedipine and related drugs) are the CA used most frequently as antihypertensives. Apart from the lowering of blood pressure CA may lead to other, theoretically beneficial, effects: regression of left ventricular and vascular hypertrophy, renal protection, weak natriuretic, weak antiplatelet, anti-ischaemic and antiatherogenic activity. Several new dihydropyridine CA have been introduced in recent years. The advantages of the newer compounds, such as amlodipine, felodipine, isradipine, lacidipine and lercanidipine, may include: vasoselectivity, hence little or no cardiodepressant activity; an improved kinetic profile, resulting in a slow onset and long duration of action, fewer side-effects such as reflex tachycardia and headache, owing to the slow onset of the antihypertensive action. For a few newer CA a predominant effect on specialized circulatory beds (renal, coronary and cerebral) has been claimed. The new CA, which are clearly lipophilic, deserve special attention. Owing to the lipophilic character of such compounds considerable concentration occurs in lipid-containing membrane depots. The CA thus concentrated are slowly released from these depots and, subsequently, reach their targets, the L-type calcium channels. This phenomenon explains both the slow onset and the long duration of action of these CA. Owing to the slow onset of action reflex tachycardia is virtually absent. The long duration of action allows satisfactory control of blood pressure in hypertensives by means of a single daily dose. A few lipophilic dihydropyridine CA are vasoselective. This property implies that at therapeutic, vasodilatory dosages no cardiodepressant activity occurs. Lercanidipine is a recently introduced example of a lipophilic and vasoselective dihydropyridine CA. It is an effective vasodilator/antihypertensive drug, with a slow onset and long duration of action, which is associated with neither reflex tachycardia nor cardiodepressant activity. Other examples of recently introduced lipophilic CA are lacidipine, barnidipine and manidipine.

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