Vlasses P H, Rotmensch H H, Swanson B N, Irvin J D, Lee R B, Koplin J R, Ferguson R K
J Clin Pharmacol. 1983 May-Jun;23(5-6):227-33. doi: 10.1002/j.1552-4604.1983.tb02729.x.
Enalapril maleate is an investigational oral prodrug whose hydrolyzed diacid metabolite is a potent angiotensin-converting enzyme inhibitor. Fourteen patients with mild to moderate hypertension were evaluated after receiving placebo, and two weeks of treatment with each of the following: enalapril maleate (20 mg b.i.d.), hydrochlorothiazide (25 mg b.i.d.), and the two in combination. In comparison to placebo, the magnitudes of the blood pressure reduction after enalapril and hydrochlorothiazide alone were comparable. The reduction in blood pressure following enalapril was evident throughout the 12-hour dosing interval. The combination of enalapril and hydrochlorothiazide resulted in a marked further reduction in blood pressure that was greater than that predicted from the responses to the individual drugs (P less than 0.05). Biochemical parameters confirmed inhibition of angiotensin-converting enzyme during enalapril treatment; serum angiotensin-converting enzyme activity proved an excellent monitor of compliance. Enalapril was generally well tolerated. Adverse effects included symptomatic hypotension in three patients when enalapril was first added to hydrochlorothiazide and hyperesthesia of the oral mucosa without a loss of taste in one patient on enalapril. Enalapril maleate alone and especially in combination with hydrochlorothiazide appears to be an effective, well-tolerated converting enzyme inhibitor with at least a 12-hour duration of action.
马来酸依那普利是一种试验性口服前体药物,其水解后的二酸代谢产物是一种强效血管紧张素转换酶抑制剂。对14例轻度至中度高血压患者先给予安慰剂,然后分别用以下药物治疗两周:马来酸依那普利(20毫克,每日两次)、氢氯噻嗪(25毫克,每日两次)以及二者联用。与安慰剂相比,依那普利和氢氯噻嗪单独使用时血压降低幅度相当。依那普利给药后12小时的整个给药间隔期内血压均有明显下降。依那普利与氢氯噻嗪联用导致血压进一步显著降低,且大于根据单药反应所预测的降幅(P小于0.05)。生化参数证实依那普利治疗期间血管紧张素转换酶受到抑制;血清血管紧张素转换酶活性是监测依从性的良好指标。依那普利总体耐受性良好。不良反应包括首次将依那普利加至氢氯噻嗪治疗时3例患者出现症状性低血压,以及1例服用依那普利的患者出现口腔黏膜感觉过敏但味觉未丧失。单独使用马来酸依那普利,尤其是与氢氯噻嗪联用,似乎是一种有效且耐受性良好的转换酶抑制剂,作用持续时间至少为12小时。