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钙拮抗剂与动脉粥样硬化

Calcium antagonists and atherosclerosis.

作者信息

Schachter M

机构信息

Department of Clinical Pharmacology, Imperial College School of Medicine at St. Mary's, London, UK.

出版信息

Int J Cardiol. 1997 Dec 31;62 Suppl 2:S9-15. doi: 10.1016/s0167-5273(97)00236-2.

Abstract

Calcium channel blockers (CCBs) have several properties which may have beneficial effects on the development of atherosclerosis. These include inhibition of vascular smooth muscle cell (SMC) proliferation and migration; inhibition of calcium influx into the vascular wall; reduction of extracellular matrix synthesis; promotion of uptake and breakdown of low-density lipoproteins; protection of lipoproteins from oxidative modification; maintenance of endothelial cell function; inhibition of platelet activation; and reduction of blood pressure. Although some of these effects are only seen at high drug concentrations, the great majority of reports indicate that CCBs can attenuate atherogenesis in animal models, notably the cholesterol-fed rabbit. Several clinical trials have now attempted to determine the efficacy of these drugs in human atheromatous disease. The outcome of these studies, including the International Nifedipine Trial of Antiatherosclerotic Therapy (INTACT), the Montreal Nicardipine Trial, and the Multicenter Isradipine/Diuretic Atherosclerosis Study (MIDAS), are summarized in this review, in the context of trials currently in progress. The emerging evidence suggests that an antiatherosclerotic action can be demonstrated in patients but the extent and clinical importance of this effect have yet to be fully established.

摘要

钙通道阻滞剂(CCBs)具有多种特性,这些特性可能对动脉粥样硬化的发展产生有益影响。这些特性包括抑制血管平滑肌细胞(SMC)的增殖和迁移;抑制钙流入血管壁;减少细胞外基质合成;促进低密度脂蛋白的摄取和分解;保护脂蛋白免受氧化修饰;维持内皮细胞功能;抑制血小板活化;以及降低血压。尽管其中一些作用仅在高药物浓度下才会出现,但绝大多数报告表明,CCBs可以在动物模型中减弱动脉粥样硬化的发生,尤其是在喂食胆固醇的兔子模型中。现在已有多项临床试验试图确定这些药物在人类动脉粥样硬化疾病中的疗效。在本综述中,结合当前正在进行的试验,总结了这些研究的结果,包括国际硝苯地平抗动脉粥样硬化治疗试验(INTACT)、蒙特利尔尼卡地平试验和多中心伊拉地平/利尿剂动脉粥样硬化研究(MIDAS)。新出现的证据表明,在患者中可以证明其具有抗动脉粥样硬化作用,但这种作用的程度和临床重要性尚未完全确定。

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