Haller H, Cosentino F, Lüscher T F
Cardiovascular Center, University Hospital, Institute of Physiology, University of Zurich, Zurich, Switzerland.
Drugs R D. 2002;3(5):311-23. doi: 10.2165/00126839-200203050-00005.
Lacidipine, a third generation dihydropyridine calcium antagonist, has demonstrated pronounced anti-atherosclerotic activity in preclinical studies. The drug can act at several stages within the atherosclerotic process, utilising its antihypertensive and antioxidant properties to protect hypertensive animals against mortality and vascular damage, to reduce cholesterol levels from the vessel wall of hypercholesterolaemic animals, and to reduce the progression of existing atherosclerotic lesions. The clinical benefit of lacidipine in atherosclerosis has recently been confirmed in humans in a large, multicentre, comparative, 4-year clinical trial involving patients with mild to moderate hypertension. The European Lacidipine Study on Atherosclerosis (ELSA) showed that lacidipine was able to slow the progression of atherosclerosis, measured as carotid intimato-media thickness, by 40% compared with atenolol (p = 0.0073). Although further comparative trials are needed, based on the results of ELSA, lacidipine is likely to become a promising therapeutic agent for atherosclerosis.
拉西地平是第三代二氢吡啶类钙拮抗剂,在临床前研究中已显示出显著的抗动脉粥样硬化活性。该药物可在动脉粥样硬化过程的多个阶段发挥作用,利用其降压和抗氧化特性来保护高血压动物免于死亡和血管损伤,降低高胆固醇血症动物血管壁中的胆固醇水平,并减少现有动脉粥样硬化病变的进展。最近,在一项针对轻度至中度高血压患者的大型、多中心、对比性4年临床试验中,已证实拉西地平对人类动脉粥样硬化具有临床益处。欧洲拉西地平动脉粥样硬化研究(ELSA)表明,与阿替洛尔相比,拉西地平能够使以颈动脉内膜中层厚度衡量的动脉粥样硬化进展减缓40%(p = 0.0073)。尽管还需要进一步的对比试验,但基于ELSA的结果,拉西地平可能会成为一种有前景的动脉粥样硬化治疗药物。