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潜在抗抑郁药咪唑的行为药理学

Behavioural pharmacology of imidazole, a potential antidepressant agent.

作者信息

Ferrari F

出版信息

Arch Int Pharmacodyn Ther. 1985 Oct;277(2):303-12.

PMID:4062441
Abstract

Imidazole (IMID) inhibited (+/-) N-n-propylnorapomorphine (NPA) and BHT-920 induced penile erections (PE) and stretching and yawning (SY) in rats as well as apomorphine (APO) induced hypothermia in mice, enhanced shock-elicited aggressiveness in rats and antagonized sleep induced by clonidine in chicks. IMID moreover displayed activity in behavioural tests used in specific screening for antidepressants, potentiating yohimbine toxicity in mice and antagonizing immobility time in the despair test, with a potency in some cases equal to imipramine. IMID per se, depressed motor activity in both mice and rats. The possible mechanism of action and receptors involved are briefly discussed as well as IMID's profile as an antidepressant drug.

摘要

咪唑(IMID)可抑制大鼠中(±)N-正丙基去甲阿扑吗啡(NPA)和BHT-920诱导的阴茎勃起(PE)以及伸展和打哈欠(SY),还可抑制小鼠中阿扑吗啡(APO)诱导的体温过低,增强大鼠电击诱发的攻击性,并拮抗可乐定诱导的雏鸡睡眠。此外,IMID在用于抗抑郁药特异性筛选的行为测试中表现出活性,增强小鼠育亨宾毒性并拮抗绝望试验中的不动时间,在某些情况下其效力与丙咪嗪相当。IMID本身会降低小鼠和大鼠的运动活性。本文简要讨论了其可能的作用机制和涉及的受体,以及IMID作为抗抑郁药的概况。

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