Robinson Dean M, Curran Monique P, Lyseng-Williamson Katherine A
Wolters Kluwer Health, Adis, Auckland, New Zealand.
Drugs. 2007;67(9):1359-78. doi: 10.2165/00003495-200767090-00008.
Imidapril (Tanatril), through its active metabolite imidaprilat, acts as an ACE inhibitor to suppress the conversion of angiotensin I to angiotensin II and thereby reduce total peripheral resistance and systemic blood pressure (BP). In clinical trials, oral imidapril was an effective antihypertensive agent in the treatment of mild to moderate essential hypertension. Some evidence suggests that imidapril also improves exercise capacity in patients with chronic heart failure (CHF) and reduces urinary albumin excretion rate in patients with type 1 diabetes mellitus. Imidapril was well tolerated, with a lower incidence of dry cough than enalapril or benazepril, and is a first choice ACE inhibitor for the treatment of mild to moderate essential hypertension.
咪达普利(达爽)通过其活性代谢产物咪达普利拉发挥作用,作为一种血管紧张素转换酶(ACE)抑制剂,抑制血管紧张素I向血管紧张素II的转化,从而降低总外周阻力和体循环血压(BP)。在临床试验中,口服咪达普利是治疗轻至中度原发性高血压的有效抗高血压药物。一些证据表明,咪达普利还可改善慢性心力衰竭(CHF)患者的运动能力,并降低1型糖尿病患者的尿白蛋白排泄率。咪达普利耐受性良好,干咳发生率低于依那普利或苯那普利,是治疗轻至中度原发性高血压的首选ACE抑制剂。