Baum T, Watkins R W, Sybertz E J, Ahn H S, Nelson S, Coleman W, Tedesco R, Pula K K, Rivelli M, Sabin C
Arch Int Pharmacodyn Ther. 1987 Apr;286(2):230-45.
SCH 33844 is a new, potent and long-acting inhibitor of angiotensin converting enzyme (ACE). Antihypertensive, hemodynamic and autonomic actions of SCH 33844 were examined in the present series of experiments. Oral administration of 0.3-30 mg/kg reduced blood pressure of spontaneously hypertensive rats. The magnitude of the response was significantly enhanced by pretreatment of the animals with hydrochlorothiazide. Blood pressure remained significantly depressed 24 hr following doses of 3 and 10 mg/kg. Administration of SCH 33844 (3 mg/kg) twice daily to nonpretreated rats or once daily to diuretic-pretreated animals for 5 days resulted in a progressive decrease in blood pressure. The compound did not reduce blood pressure in nephrectomized rats demonstrating the dependence of its action on renal renin. SCH 33844 (1-10 mg/kg orally) also produced dose-related decreases in pressure in diuretic-pretreated conscious normotensive dogs. However, only a small fall in pressure occurred in non-pretreated dogs. Hemodynamic actions were examined in anesthetized dogs. SCH 33844 (1 mg/kg i.v.) reduced blood pressure, increased cardiac output and caused a large fall in peripheral resistance. Autonomic actions were assessed in pithed rats. The compound (10 mg/kg orally) tended to decrease pressor responses to sympathetic activation and to i.v. norepinephrine. This profile is probably due, at least in part, to vasorelaxation following suppression of angiotensin II generation. In conclusion, SCH 33844 is a potent, long-lasting antihypertensive agent which reduces peripheral vascular resistance and possesses only slight autonomic effects.
SCH 33844是一种新型、强效且长效的血管紧张素转换酶(ACE)抑制剂。在本系列实验中研究了SCH 33844的降压、血流动力学及自主神经作用。口服0.3 - 30 mg/kg可降低自发性高血压大鼠的血压。用氢氯噻嗪预处理动物可显著增强反应幅度。给予3和10 mg/kg剂量后24小时血压仍显著降低。对未预处理的大鼠每日两次给予SCH 33844(3 mg/kg)或对用利尿剂预处理的动物每日一次给予该剂量,持续5天,导致血压逐渐下降。该化合物对肾切除大鼠无降压作用,表明其作用依赖于肾素。口服SCH 33844(1 - 10 mg/kg)也使经利尿剂预处理的清醒正常血压犬的血压出现剂量相关下降。然而,未预处理的犬仅出现小幅血压下降。在麻醉犬中研究了血流动力学作用。静脉注射SCH 33844(1 mg/kg)可降低血压、增加心输出量并导致外周阻力大幅下降。在脊髓横断大鼠中评估了自主神经作用。该化合物(口服10 mg/kg)倾向于降低对交感神经激活和静脉注射去甲肾上腺素的升压反应。这种情况可能至少部分归因于抑制血管紧张素II生成后的血管舒张。总之,SCH 33844是一种强效、长效的降压药,可降低外周血管阻力,且仅有轻微的自主神经作用。