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尼卡地平可预防慢性乙醇或氟哌啶醇诱导的对阿扑吗啡诱导的攻击行为的超敏反应。

Nicardipine protects against chronic ethanol- or haloperidol-induced supersensitivity to apomorphine-induced aggression.

作者信息

Pucilowski O, Eichelman B

机构信息

Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill 27599-7175.

出版信息

Neuropsychopharmacology. 1991 Aug;5(1):55-60.

PMID:1930612
Abstract

Affective apomorphine-induced aggression was induced in originally nonaggressive rats after withdrawal from prolonged ethanol or haloperidol treatment. If the animals were co-administered Ca(2+)-channel blockers like diltiazem or verapamil the aggressive response to apomorphine was markedly decreased. Nicardipine (2 and 5 mg/kg b.i.d.) significantly attenuated the aggression-enhancing effect of chronic ethanol or haloperidol withdrawal in nonaggressive rats. Chronic nicardipine, alone, did not enhance aggressive behavior in the nonaggressive rats. Acutely, it suppressed apomorphine-induced aggression but did not alter open field activity when injected into aggressive rats. These results demonstrate that a Ca(2+)-channel blocker of the dihydropyridine type can prevent the development of an ethanol or haloperidol-withdrawal supersensitivity to apomorphine-induced aggression. It attenuates the aggression-inducing effect of apomorphine without impairing general activity.

摘要

在长期乙醇或氟哌啶醇治疗撤药后,原本无攻击性的大鼠会出现阿扑吗啡诱导的情感性攻击行为。如果给这些动物同时使用地尔硫䓬或维拉帕米等钙通道阻滞剂,对阿扑吗啡的攻击反应会明显降低。尼卡地平(2和5毫克/千克,每日两次)显著减弱了非攻击性大鼠慢性乙醇或氟哌啶醇撤药的攻击增强效应。单独使用慢性尼卡地平不会增强非攻击性大鼠的攻击行为。急性给药时,将其注射到攻击性大鼠体内,它会抑制阿扑吗啡诱导的攻击行为,但不会改变旷场活动。这些结果表明,二氢吡啶类钙通道阻滞剂可以预防乙醇或氟哌啶醇撤药对阿扑吗啡诱导攻击的超敏反应的发展。它减弱了阿扑吗啡的攻击诱导效应,而不损害一般活动。

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