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维拉帕米在兔实验性动脉粥样硬化模型中的抗动脉粥样硬化剂量反应效应。

The antiatherogenic dose response effect of verapamil in an experimental atherosclerosis model in the rabbit.

作者信息

Lazarová Z, Edelsteinová S, Lojda Z

机构信息

Department of Pharmacodynamics and Toxicology, Pharmaceutical Faculty, Bratislava, Czechoslovakia.

出版信息

Cor Vasa. 1991;33(6):480-91.

PMID:1842941
Abstract

The aim of the study was to assess the dose dependence of the antiatherogenic effect of verapamil (Isoptin, Lek Ljubljana, Yugoslavia) in rabbits fed 1% cholesterol diet. Verapamil was administered subcutaneously at doses of 0.25, 1 and 2 mg.kg-1/day at 12-hour intervals for 8 weeks. The results indicate verapamil administered s.c. exerts a preventive anti-atherosclerotic effect only in therapeutic doses (0.25 mg.kg-1). The beneficial effect of low-dose verapamil can also be seen in the spectrum of serum lipids as the drug lowers the levels of total cholesterol and triacylglycerols. Compared with the results obtained from a group receiving diet without Ca-antagonist premedication, high doses do not reduce the extent of atheromatous plaques.

摘要

本研究的目的是评估维拉帕米(异搏定,南斯拉夫卢布尔雅那莱克制药厂生产)对喂食1%胆固醇饮食的家兔抗动脉粥样硬化作用的剂量依赖性。维拉帕米以0.25、1和2毫克·千克⁻¹/天的剂量皮下注射,每12小时一次,持续8周。结果表明,皮下注射维拉帕米仅在治疗剂量(0.25毫克·千克⁻¹)时发挥预防性抗动脉粥样硬化作用。低剂量维拉帕米的有益作用还体现在血脂谱方面,因为该药物可降低总胆固醇和三酰甘油水平。与未预先使用钙拮抗剂进行饮食治疗的组所获得的结果相比,高剂量并不能减少动脉粥样斑块的范围。

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