Rosenthal J H
Section of Pharmacotherapy, Ulm University Medical Center, Germany.
J Cardiovasc Pharmacol. 1994;24 Suppl 2:S65-9.
Cilazapril, a new angiotensin-converting enzyme (ACE) inhibitor, controls blood pressure (to 90 mm Hg or less) in patients with mild-to-moderate hypertension within 2-3 weeks of initiating treatment (2.5-5.0 mg once daily); this effect was maintained in long-term observations over 1 year. Hemodynamic investigations demonstrated that the antihypertensive action of cilazapril is induced mainly by a decrease of peripheral vascular resistance accompanied by a decrease of pulmonary capillary wedge pressure. Furthermore, cilazapril decreased left ventricular mass index in essential hypertensive patients within 6 months of therapy at doses of 2.5-5.0 mg once daily, thus reversing left ventricular hypertrophy induced by hypertension. In other studies cilazapril was shown to ameliorate glucose tolerance and insulin sensitivity in nondiabetic hypertensive patients, and in hypertensive diabetic patients improvement of renal function was observed. Incidence and severity of side effects caused by cilazapril were comparable to those seen by other ACE inhibitors. Although experimental data provide evidence for vascular, antiatherosclerotic protection by cilazapril, these effects must be proven by long-term prospective studies in humans.
西拉普利是一种新型血管紧张素转换酶(ACE)抑制剂,在轻度至中度高血压患者中,开始治疗(每日一次2.5 - 5.0毫克)后的2 - 3周内可将血压控制在90毫米汞柱或更低;在超过1年的长期观察中,这种效果得以维持。血流动力学研究表明,西拉普利的降压作用主要是由外周血管阻力降低以及肺毛细血管楔压降低引起的。此外,在原发性高血压患者中,每日一次服用剂量为2.5 - 5.0毫克的西拉普利,在治疗6个月内可降低左心室质量指数,从而逆转高血压所致的左心室肥厚。在其他研究中,西拉普利被证明可改善非糖尿病高血压患者的糖耐量和胰岛素敏感性,并且在高血压糖尿病患者中观察到肾功能有所改善。西拉普利引起的副作用发生率和严重程度与其他ACE抑制剂相当。尽管实验数据为西拉普利的血管保护和抗动脉粥样硬化作用提供了证据,但这些作用必须通过对人类进行长期前瞻性研究来证实。