Waters D, Lespérance J
Department of Medicine, Montreal Heart Institute, Quebec, Canada.
Circulation. 1992 Dec;86(6 Suppl):III111-6.
Calcium channel blockers have been shown to retard the development of atherosclerosis in rabbits fed cholesterol-rich diets. The mechanism accounting for this effect is controversial but may be by stimulation of cholesteryl ester hydrolase activity in smooth muscle cells, by amelioration of hypercholesterolemia-induced endothelial dysfunction, or by inhibition of smooth muscle cell proliferation and migration. The effect of calcium channel blockers on the evolution of coronary atherosclerosis in humans has been assessed in two clinical trials. In the Montreal Heart Institute trial, nicardipine did not influence the overall rate of progression and regression; however, nicardipine-treated patients experienced significantly less progression of minimal lesions, defined as stenoses of < or = 20% severity. In the International Nifedipine Trial on Antiatherosclerotic Therapy, nifedipine had no effect on overall progression and regression but reduced the rate of appearance of new coronary lesions. These studies constitute a potentially important new approach to the management of coronary atherosclerosis.
钙通道阻滞剂已被证明可延缓喂食富含胆固醇饮食的兔子动脉粥样硬化的发展。解释这种作用的机制存在争议,但可能是通过刺激平滑肌细胞中的胆固醇酯水解酶活性、改善高胆固醇血症诱导的内皮功能障碍,或抑制平滑肌细胞增殖和迁移。两项临床试验评估了钙通道阻滞剂对人类冠状动脉粥样硬化进展的影响。在蒙特利尔心脏研究所的试验中,尼卡地平不影响总体进展和消退率;然而,接受尼卡地平治疗的患者病变程度较轻(定义为狭窄程度≤20%)的进展明显较少。在硝苯地平抗动脉粥样硬化治疗国际试验中,硝苯地平对总体进展和消退没有影响,但降低了新冠状动脉病变的出现率。这些研究构成了一种潜在的重要的冠状动脉粥样硬化管理新方法。