Ryan M J, Boucher D M, Cohen D M, Essenburg A D, Major T C, Mertz T E, Olszewski B J, Randolph A E, Singer R M, Kaplan H R
J Pharmacol Exp Ther. 1984 Feb;228(2):312-8.
CI-907 is a new orally active nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor. Monoester (prodrug) and diacid forms produced concentration related ACE inhibition in guinea-pig serum (IC50 for monoester, 1.7 X 10(-7) M and for diacid, 2.6 X 10(-9) M). In isolated rabbit aortic rings and in rat and dog autonomic studies, CI-907 is highly specific in suppressing the contractile or pressor responses to angiotensin I. In two-kidney, one-clip Goldblatt hypertensive rats, single daily doses (0.03-30 mg/kg p.o.) produced dose-dependent decreases in blood pressure; 3 mg/kg lowered blood pressure to normotensive levels. In the spontaneously hypertensive rat, subacute administration of CI-907 (30 mg/kg/day for 5 days) produced the same decrease in blood pressure as that obtained in the renal hypertensive rat. In diuretic-pretreated renal hypertensive dogs, 10 mg/kg normalized blood pressure. For equivalent drops in blood pressure, heart rate increases were less in CI-907 than in enalapril-treated renal hypertensive dogs. No side effects were observed with CI-907 in any of the conscious animals. The antihypertensive response to CI-907 (0.03-1.0 mg/kg p.o.) was found to correlate with inhibition of vascular tissue ACE, but not plasma or brain ACE in two-kidney, one-clip renal hypertensive rats. These studies indicate that CI-907 is a potent antihypertensive agent with a heart rate profile different from enalapril.
CI-907是一种新型口服活性非巯基血管紧张素转换酶(ACE)抑制剂。单酯(前体药物)和二酸形式在豚鼠血清中产生与浓度相关的ACE抑制作用(单酯的IC50为1.7×10⁻⁷M,二酸的IC50为2.6×10⁻⁹M)。在离体兔主动脉环以及大鼠和犬的自主神经研究中,CI-907在抑制对血管紧张素I的收缩或升压反应方面具有高度特异性。在两肾一夹型Goldblatt高血压大鼠中,每日单次口服剂量(0.03 - 30mg/kg)可使血压呈剂量依赖性下降;3mg/kg可使血压降至正常血压水平。在自发性高血压大鼠中,亚急性给予CI-907(30mg/kg/天,共5天)产生的血压下降与肾性高血压大鼠相同。在经利尿剂预处理的肾性高血压犬中,10mg/kg可使血压恢复正常。对于同等程度的血压下降,CI-907引起的心率增加低于依那普利治疗的肾性高血压犬。在任何清醒动物中,CI-907均未观察到副作用。在两肾一夹型肾性高血压大鼠中,发现CI-907(0.03 - 1.0mg/kg口服)的降压反应与血管组织ACE的抑制相关,但与血浆或脑ACE无关。这些研究表明,CI-907是一种强效降压药,其心率变化特点与依那普利不同。