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β-肾上腺素能阻滞剂对犬对地尔硫䓬或维拉帕米心血管反应的影响。

The effect of beta-adrenergic blockade on the cardiovascular response to diltiazem or verapamil in dogs.

作者信息

Sullivan K B, Kapur P A

出版信息

Anesth Analg. 1986 Nov;65(11):1099-106.

PMID:3021022
Abstract

Diltiazem or verapamil were each given at two different infusion rates to pentobarbital-anesthetized dogs with or without a concurrent infusion of propranolol. Changes in cardiovascular function, in reflex activation as reflected by circulating catecholamine levels, and in the chronotropic response to an exogenous beta-adrenergic agonist, isoproterenol, were measured. When administered alone, diltiazem or verapamil, at plasma concentrations of 160 and 370 ng/ml, or 230 and 500 ng/ml, respectively, prolonged atrioventricular conduction and caused systemic vasodilation with a decrease in mean arterial pressure. Cardiac index increased, associated with an increase in arterial norepinephrine level. Heart rate increased with the lower level of verapamil; left ventricular dP/dt increased with both levels of verapamil and at the higher level of diltiazem. Plasma propranolol levels of approximately 35 ng/ml were well tolerated in the absence of diltiazem or verapamil. When added to diltiazem or verapamil, propranolol resulted in an increase in systemic vascular resistance to near control values; a decrease in cardiac index, left ventricular dP/dt, and heart rate; and worsened atrioventricular conduction. Three of nine animals in the high verapamil-propranolol group were unable to maintain a mean arterial pressure greater than 50 mm Hg, and developed a low cardiac index with an elevated systemic vascular resistance, despite very high levels of circulating catecholamines. Compared to the anesthetized state, greater amounts of isoproterenol were needed to effect the same increase in heart rate with the addition of diltiazem, verapamil, or propranolol alone.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将地尔硫䓬或维拉帕米分别以两种不同的输注速率给予戊巴比妥麻醉的犬,同时或不同时输注普萘洛尔。测量心血管功能的变化、循环儿茶酚胺水平反映的反射激活情况以及对外源性β-肾上腺素能激动剂异丙肾上腺素的变时反应。单独给药时,地尔硫䓬或维拉帕米,血浆浓度分别为160和370 ng/ml,或230和500 ng/ml,可延长房室传导并引起全身血管舒张,平均动脉压降低。心脏指数增加,与动脉去甲肾上腺素水平升高有关。维拉帕米较低水平时心率增加;维拉帕米两种水平及地尔硫䓬较高水平时左心室dp/dt增加。在没有地尔硫䓬或维拉帕米的情况下,血浆普萘洛尔水平约为35 ng/ml时耐受性良好。当加入地尔硫䓬或维拉帕米时,普萘洛尔导致全身血管阻力增加至接近对照值;心脏指数、左心室dp/dt和心率降低;房室传导恶化。高剂量维拉帕米-普萘洛尔组的9只动物中有3只无法维持平均动脉压大于50 mmHg,尽管循环儿茶酚胺水平很高,但仍出现低心脏指数和全身血管阻力升高。与麻醉状态相比,单独添加地尔硫䓬、维拉帕米或普萘洛尔时,需要更大剂量的异丙肾上腺素才能使心率产生相同程度的增加。(摘要截短于250字)

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