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苯环利定诱导的大鼠运动活动被伏隔核的6-羟基多巴胺损伤所阻断:与其他精神运动性兴奋剂的比较。

Phencyclidine-induced locomotor activity in the rat is blocked by 6-hydroxydopamine lesion of the nucleus accumbens: comparisons to other psychomotor stimulants.

作者信息

French E D, Vantini G

出版信息

Psychopharmacology (Berl). 1984;82(1-2):83-8. doi: 10.1007/BF00426386.

Abstract

The present study was primarily designed to explore the relationship between phencyclidine(PCP)-induced hyperactivity and the mesolimbic dopamine (DA) system. In addition, the motor-activating and behavioral effects of amphetamine (1.5 mg/kg), SKF-10,047 (25.0 mg/kg), scopolamine (1.0 mg/kg), and caffeine (10.0 mg/kg) were also measured and compared to PCP action. While all compounds produced a moderate to large degree of hyperactivity with varying time courses for effect, gross behavioral observations indicated a greater similarity between PCP and SKF-10,047 than between any of the other drugs. Following bilateral 6-hydroxydopamine lesions of the nucleus accumbens the robust locomotor-stimulating action of 5 mg/kg PCP was significantly reduced. Such lesions also successfully prevented amphetamine- and SKF-10,047-induced hyperactivity, but not the behavioral activation produced by scopolamine or caffeine. These results suggest that PCP and SKF-10,047, like amphetamine, elicit locomotor activity through presynaptic DA mechanisms within the mesolimbic system.

摘要

本研究主要旨在探讨苯环利定(PCP)诱发的多动与中脑边缘多巴胺(DA)系统之间的关系。此外,还测量了苯丙胺(1.5毫克/千克)、SKF-10,047(25.0毫克/千克)、东莨菪碱(1.0毫克/千克)和咖啡因(10.0毫克/千克)的运动激活和行为效应,并与PCP的作用进行比较。虽然所有化合物都产生了中度到高度的多动,且效应的时间进程各不相同,但总体行为观察表明,PCP与SKF-10,047之间的相似性大于其他任何药物之间的相似性。伏隔核经双侧6-羟基多巴胺损伤后,5毫克/千克PCP的强烈运动刺激作用显著降低。这种损伤也成功地阻止了苯丙胺和SKF-10,047诱发的多动,但没有阻止东莨菪碱或咖啡因产生的行为激活。这些结果表明,PCP和SKF-10,047与苯丙胺一样,通过中脑边缘系统内的突触前DA机制引发运动活动。

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