Waeber G, Burnier M, Porchet M, Nussberger J, Waeber B, Brunner H R
Division of Hypertension, University Hospital Lausanne, Switzerland.
Eur J Clin Pharmacol. 1989;36(6):587-91. doi: 10.1007/BF00637741.
A new, orally active angiotensin converting enzyme (ACE) inhibitor, CGS 16617, has been evaluated in normotensive subjects during acute and prolonged administration. Single ascending doses of CGS 16617 20 to 100 mg were given to 9 normotensive volunteers at one week intervals and the changes in blood pressure, plasma ACE and renin activity were examined up to 72 h after drug intake. Also, CGS 16617 50 mg/day or placebo were given for 30 days to 8 and 6 normotensive subjects, respectively, maintained on an unrestricted salt diet. Blood pressure was measured daily in the office and ambulatory blood pressure profiles were also obtained before, during and after therapy, using the Remler M 2000 blood pressure recording system. CGS 16617 was an effective and long lasting ACE inhibitor. It did not induce a consistent change in blood pressure, but, the individual responses were very variable and several subjects experienced a clear decrease in the average of the blood pressures recorded during the daytime.
一种新型口服活性血管紧张素转换酶(ACE)抑制剂CGS 16617,已在血压正常的受试者中进行了急性和长期给药评估。将20至100毫克的CGS 16617单剂量递增给药于9名血压正常的志愿者,给药间隔为一周,并在服药后长达72小时检查血压、血浆ACE和肾素活性的变化。此外,分别给予8名和6名血压正常的受试者CGS 16617 50毫克/天或安慰剂,持续30天,受试者维持不限盐饮食。在办公室每天测量血压,并使用Remler M 2000血压记录系统在治疗前、治疗期间和治疗后获取动态血压曲线。CGS 16617是一种有效且长效的ACE抑制剂。它并未引起血压的一致变化,但个体反应差异很大,有几名受试者白天记录的平均血压明显下降。