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多他利嗪对犬外周循环、肺循环及心脏动力学的影响。

Effects of dotarizine on peripheral and pulmonary circulation and cardiac dynamics in dogs.

作者信息

Cartheuser C F, Brasó A, Sacristán A, Ortiz J A

机构信息

Department of Pharmacology, Research Centre, Ferrer International, Barcelona, Spain.

出版信息

Pharmacology. 1994 Mar;48(3):187-93. doi: 10.1159/000139178.

Abstract

The cardiovascular effects of dotarizine in 10-min intravenous infusions were studied in thiopental-anesthetized dogs. The effects of dotarizine 0.024 mg/kg/min almost paralleled those of saline controls; 0.079 mg/kg/min dotarizine significantly raised the stroke index and ejection fraction, and, at a rate of 0.25 mg/kg/min, further effects appeared and were dose-dependent. Dotarizine produced arterial dilation in both systemic and pulmonary circulation: the total peripheral resistance dropped, and femoral artery flow rose; aortic and pulmonary artery mean and diastolic pressures declined, and systolic pressures remained almost stable. A trend of bradycardia and pulmonary artery pressure reduction persisted for 30 min. As compared with the reduced total peripheral resistance, aortic pressure fell only moderately because of rising cardiac output due to a higher ejection fraction and stroke volume. Cardiac preload tended to decline; contractility tended to increase. Cardiac performance remained stable while myocardial oxygen consumption tended to fall, as did the pressure-rate product and the tension time index. Dotarizine exerted direct cardiovascular effects similar to those of the 5-HT2-receptor antagonist ketanserin and, more generally, to calcium channel blockers rather than to alpha-adrenoceptor blockers.

摘要

在硫喷妥钠麻醉的犬中研究了多他利嗪10分钟静脉输注的心血管效应。0.024毫克/千克/分钟的多他利嗪效应几乎与生理盐水对照组平行;0.079毫克/千克/分钟的多他利嗪显著提高了每搏指数和射血分数,并且以0.25毫克/千克/分钟的速率,出现了进一步的效应且呈剂量依赖性。多他利嗪在体循环和肺循环中均引起动脉扩张:总外周阻力下降,股动脉血流增加;主动脉和肺动脉平均压及舒张压下降,收缩压几乎保持稳定。心动过缓和肺动脉压降低的趋势持续了30分钟。与总外周阻力降低相比,由于射血分数和每搏量增加导致心输出量上升,主动脉压仅适度下降。心脏前负荷趋于下降;收缩力趋于增加。心脏功能保持稳定,而心肌耗氧量趋于下降,压力-心率乘积和张力时间指数也是如此。多他利嗪产生的直接心血管效应类似于5-羟色胺2受体拮抗剂酮色林,更一般地说,类似于钙通道阻滞剂而非α-肾上腺素能受体阻滞剂。

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