Hansson L
Department of Medicine, University of Göteborg, Ostra Hospital, Sweden.
Drugs. 1990;40 Suppl 2:10-4. doi: 10.2165/00003495-199000402-00005.
Calcium antagonists, particularly those derived from the dihydropyridine class, have shown remarkable efficacy in the treatment of hypertension and other cardiovascular disorders. This review will concentrate on the use of one of the newer compounds in this category, isradipine, in the treatment of arterial hypertension. Isradipine is a calcium antagonist with marked vascular selectivity and, in practical terms, is devoid of cardiac effects. Its usefulness in hypertension is well documented, both when used as single drug treatment and in combination with other agents, particularly beta-blockers. Isradipine is well tolerated, does not cause metabolic disturbances and, apart from the typical dihydropyridine-type vascular adverse effects, e.g. flushing and ankle oedema, it does not cause any specific side effect. Some results obtained with isradipine in animal studies, e.g. the antiatherosclerotic effect and the brain tissue preserving effect seen in experimental stroke, appear to hold great promise for future important clinical applications for isradipine.
钙拮抗剂,尤其是二氢吡啶类衍生的钙拮抗剂,已在高血压及其他心血管疾病的治疗中显示出显著疗效。本综述将聚焦于该类别中较新的一种化合物——伊拉地平在动脉高血压治疗中的应用。伊拉地平是一种具有显著血管选择性的钙拮抗剂,实际上无心脏效应。无论是作为单一药物治疗还是与其他药物(尤其是β受体阻滞剂)联合使用,其在高血压治疗中的有效性都有充分记录。伊拉地平耐受性良好,不会引起代谢紊乱,除了典型的二氢吡啶类血管不良反应,如潮红和踝部水肿外,不会引起任何特殊副作用。伊拉地平在动物研究中获得的一些结果,如抗动脉粥样硬化作用以及在实验性中风中观察到的脑组织保护作用,似乎为伊拉地平未来的重要临床应用带来了巨大希望。