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血管紧张素转换酶抑制剂对小鼠的益智作用。

Nootropic effects of ACE inhibitors in mice.

作者信息

Mondadori C, Etienne P

机构信息

Ciba-Geigy, Pharmaceutical Research Department, Basel, Switzerland.

出版信息

Psychopharmacology (Berl). 1990;100(3):301-7. doi: 10.1007/BF02244597.

Abstract

The angiotensin converting enzyme (ACE) inhibitors captopril and enalapril and the nootropic piracetam reduced the amnesiogenic effects of cerebral electroshock treatment in mice. These compounds also directly improved passive-avoidance learning if administered before the learning trial. When given immediately after the learning trial, captopril and piracetam were active, but not enalapril. Captopril, but neither enalapril nor piracetam, facilitated memory retrieval after a 2-month retention interval. Unlike those of piracetam, the memory-improving effects of captopril and enalapril are not established by aldosterone-receptor blockade, suggesting that the two types of drug act via different mechanisms of action.

摘要

血管紧张素转换酶(ACE)抑制剂卡托普利和依那普利以及促智药吡拉西坦可减轻小鼠脑电击治疗的致失忆作用。如果在学习试验前给药,这些化合物还能直接改善被动回避学习。在学习试验后立即给药时,卡托普利和吡拉西坦有效,但依那普利无效。在2个月的保留期后,卡托普利促进了记忆恢复,但依那普利和吡拉西坦均无此作用。与吡拉西坦不同,卡托普利和依那普利的记忆改善作用并非通过醛固酮受体阻断来实现,这表明这两种药物的作用机制不同。

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