Suppr超能文献

维拉帕米和硝苯地平的内在及反射作用:通过无创技术和自主神经阻滞在正常受试者中的评估

Intrinsic and reflex actions of verapamil and nifedipine: assessment in normal subjects by noninvasive techniques and autonomic blockade.

作者信息

Stern H C, Matthews J H, Belz G G

出版信息

Eur J Clin Pharmacol. 1986;29(5):541-7. doi: 10.1007/BF00635890.

Abstract

To determine the intrinsic and reflex activities of calcium antagonists, 8 healthy volunteers were administered single doses of verapamil 10 mg i.v. and nifedipine 20 mg sublingually alone and during autonomic blockade (atropine 0.04 mg/kg and propranolol 0.2 mg/kg). Heart rate, PQ-time, systolic time intervals, blood pressure, and left ventricular echocardiograms were used to measure the pharmacodynamic effects, which were evaluated by multivariate analysis of variance. In general the effects of verapamil were most distinct when the 10-min infusion ended, while nifedipine acted after a latent period of 9 minutes. Both calcium antagonists given alone induced almost identical increases in heart rate and cardiac output and decreases in total peripheral resistance. Nifedipine also reduced systolic wall stress and increased fractional shortening, while verapamil prolonged systolic time intervals and PQ-time and reduced fractional shortening. During autonomic blockade, nifedipine no longer had a significant effect on these parameters. However, after the blockade verapamil led to marked decrease in heart rate, cardiac output, blood pressure and systolic wall stress; total peripheral resistance and fractional shortening were not changed, and the systolic time intervals and PQ-time were prolonged as after verapamil alone. It is concluded that both calcium antagonists stimulate distinct sympathetic reflexes, which may modify or even reverse their intrinsic actions. The effects of nifedipine on the cardiovascular system are considered to result from a reduction in peripheral vascular tone, whereas the effects of verapamil can be attributed to cardiac (negative inotropic, chronotropic and dromotropic) and peripheral vascular actions.

摘要

为了确定钙拮抗剂的内在活性和反射活性,8名健康志愿者分别静脉注射10mg维拉帕米、舌下含服20mg硝苯地平,且在自主神经阻滞(阿托品0.04mg/kg和普萘洛尔0.2mg/kg)期间进行单剂量给药。使用心率、PQ间期、收缩期时间间期、血压和左心室超声心动图来测量药效学效应,并通过多变量方差分析进行评估。一般来说,维拉帕米在10分钟输注结束时效果最为明显,而硝苯地平在9分钟的潜伏期后起效。单独给予两种钙拮抗剂均能使心率和心输出量几乎相同地增加,总外周阻力降低。硝苯地平还降低了收缩期壁应力并增加了缩短分数,而维拉帕米延长了收缩期时间间期和PQ间期并降低了缩短分数。在自主神经阻滞后,硝苯地平对这些参数不再有显著影响。然而,阻滞后维拉帕米导致心率、心输出量、血压和收缩期壁应力显著降低;总外周阻力和缩短分数未改变,收缩期时间间期和PQ间期与单独给予维拉帕米后一样延长。结论是两种钙拮抗剂均刺激不同的交感神经反射,这可能会改变甚至逆转它们的内在作用。硝苯地平对心血管系统的作用被认为是由于外周血管张力降低所致,而维拉帕米的作用可归因于心脏(负性变力、变时和变传导)和外周血管作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验