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苄普地尔、地尔硫䓬、硝苯地平和维拉帕米对麻醉犬血流动力学参数及心肌氧耗的比较作用

Comparative effects of bepridil, diltiazem, nifedipine and verapamil on haemodynamic parameters and myocardial oxygen consumption in anaesthetized dogs.

作者信息

Beaughard M, Michelin M T, Tisne-Versailles J, Lamar J C

出版信息

Arch Int Pharmacodyn Ther. 1986 Dec;284(2):276-96.

PMID:3493742
Abstract

The haemodynamic effects of 4 calcium antagonists, bepridil (1.25 to 5 mg/kg i.v.), diltiazem (0.1 to 0.3 mg/kg i.v.), nifedipine (0.01 to 0.03 mg/kg i.v.) and verapamil (0.1 to 0.3 mg/kg i.v.) were compared in anaesthetized open-chest dogs. The following parameters were measured: sinusal coronary blood flow (SCBF), total coronary vascular resistance (TCVR), aortic blood pressure, heart rate, left dP/dt max, amplitude of right ventricular contraction, double product, myocardial oxygen consumption (MVO2) and arterial and coronary venous blood gases (pO2 and pCO2) and pH. All 4 substances increased SCBF and decreased TCVR. The greatest effects, taking into account relative dose size, were obtained with nifedipine and verapamil. These 2 substances also had the greatest effect on systemic vasodilatation, as reflected by hypotension. The 4 substances had a direct negative chronotropic effect on the myocardium, an effect which was masked by reflex sympathetic stimulation and decreased vagal tone secondary to a drop in blood pressure. The most marked negative chronotropic effects were seen with diltiazem, verapamil and bepridil in that order. Nifedipine and verapamil produced the greatest negative inotropic effects, whereas diltiazem had very little effect on this parameter. The direct consequence of these haemodynamic effects of the 4 substances was to improve oxygenation of the myocardium. The most durable effect on PvO2 was seen with nifedipine and verapamil. The findings demonstrate not only the heterogeneous action of the 4 calcium antagonists, but also the influence of the experimental conditions on the effects obtained with these substances.

摘要

在麻醉开胸犬中比较了4种钙拮抗剂(苄普地尔,静脉注射1.25至5mg/kg;地尔硫䓬,静脉注射0.1至0.3mg/kg;硝苯地平,静脉注射0.01至0.03mg/kg;维拉帕米,静脉注射0.1至0.3mg/kg)的血流动力学效应。测量了以下参数:窦性冠状动脉血流量(SCBF)、总冠状动脉血管阻力(TCVR)、主动脉血压、心率、左心室dp/dt max、右心室收缩幅度、双乘积、心肌耗氧量(MVO2)以及动脉和冠状静脉血气(pO2和pCO2)和pH值。所有4种物质均增加了SCBF并降低了TCVR。考虑到相对剂量大小,硝苯地平和维拉帕米产生的效应最大。这两种物质对全身血管舒张也有最大的作用,表现为低血压。这4种物质对心肌有直接的负性变时作用,这种作用被反射性交感神经刺激所掩盖,并且由于血压下降导致迷走神经张力降低。负性变时作用最明显的依次是地尔硫䓬、维拉帕米和苄普地尔。硝苯地平和维拉帕米产生的负性变力作用最大,而地尔硫䓬对该参数影响很小。这4种物质这些血流动力学效应的直接后果是改善了心肌的氧合。硝苯地平和维拉帕米对混合静脉血氧分压(PvO2)的作用最持久。这些发现不仅证明了4种钙拮抗剂作用的异质性,还证明了实验条件对这些物质所获效应的影响。

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