Hansson L
Department of Medicine, University of Gothenburg, Sweden.
Acta Anaesthesiol Scand Suppl. 1993;99:26-8. doi: 10.1111/j.1399-6576.1993.tb03820.x.
Isradipine is a new dihydropyridine-derived calcium antagonist. It possesses marked vascular selectivity, resulting in a powerful vasodilating action, whereas, in practical terms, it is devoid of cardiac effects. The usefulness of isradipine in the treatment of arterial hypertension is well documented, both when used as single-drug treatment and in combination with other agents, particularly, beta-blockers. Isradipine is well tolerated and does not negatively affect quality of life or capacity for physical exercise. It does not cause metabolic disturbances and, apart from the typical dihydropyridine-type vascular side-effects, specifically, flushing and ankle oedema, there are no specific adverse effects. Even ankle oedema is apparently relatively rare with this compound. Studies in animal models show that isradipine has a potent anti-atherosclerotic effect, and a brain tissue-preserving effect after experimental stroke, in doses that are relevant for antihypertensive treatment. If such results can be confirmed in humans, they will undoubtedly be of great clinical importance.
伊拉地平是一种新型二氢吡啶类钙拮抗剂。它具有显著的血管选择性,从而产生强大的血管舒张作用,而实际上,它对心脏没有影响。伊拉地平用于治疗动脉高血压的有效性已有充分记录,无论是作为单一药物治疗还是与其他药物联合使用,特别是与β受体阻滞剂联合使用时。伊拉地平耐受性良好,不会对生活质量或体育锻炼能力产生负面影响。它不会引起代谢紊乱,除了典型的二氢吡啶类血管副作用,特别是潮红和踝部水肿外,没有其他特定的不良反应。即使是踝部水肿,使用这种化合物时显然也相对少见。动物模型研究表明,在与抗高血压治疗相关的剂量下,伊拉地平具有强大的抗动脉粥样硬化作用以及实验性中风后的脑组织保护作用。如果这些结果能够在人体中得到证实,无疑将具有重大的临床意义。