Vlasses P H, Ferguson R K, Chatterjee K
Pharmacotherapy. 1982 Jan-Feb;2(1):1-17. doi: 10.1002/j.1875-9114.1982.tb03167.x.
Captopril, a competitive antagonist of angiotensin converting enzyme, has been marketed in the United States for the treatment of resistant hypertension. Despite extensive study, its exact mechanism of action remains unclear; decreased renin-angiotensin-aldosterone and sympathoadrenal system activity as well as increased bradykinin and prostaglandin E and F activity have been postulated. The drug decreases peripheral vascular resistance. Controlled trials in resistant hypertension of various etiologies and chronic congestive heart failure have demonstrated sustained effectiveness and therapeutic benefits. Side effects include skin rash, loss of taste, proteinuria, and leukopenia; higher doses and concomitant renal dysfunction appear to be predisposing factors. The benefit-to-risk ratio for captopril clearly justifies its use in resistant cases of hypertension and congestive heart failure, but further experience is needed to evaluate its use in milder forms of these diseases.
卡托普利是一种血管紧张素转换酶竞争性拮抗剂,已在美国上市用于治疗顽固性高血压。尽管进行了广泛研究,但其确切作用机制仍不清楚;有人推测它可降低肾素-血管紧张素-醛固酮和交感肾上腺系统活性,同时增加缓激肽以及前列腺素E和F的活性。该药可降低外周血管阻力。针对各种病因的顽固性高血压和慢性充血性心力衰竭的对照试验已证明其具有持续有效性和治疗益处。副作用包括皮疹、味觉丧失、蛋白尿和白细胞减少;高剂量和合并肾功能不全似乎是诱发因素。卡托普利的效益风险比明确证明其可用于高血压和充血性心力衰竭的顽固性病例,但需要更多经验来评估其在这些疾病较轻形式中的应用。