Neal H, Bond A
Neuropharmacology. 1985 Apr;24(4):317-23. doi: 10.1016/0028-3908(85)90137-6.
An automated technique for the continuous analysis of different frequency bands of the electrocorticogram (ECoG) of the rat has been used to quantify the actions of phencyclidine (PCP) and various other stimulant drugs. It has been demonstrated that phencyclidine, etoxadrol and LY154045 produced similar changes in the individual frequency bands whereas amphetamine and apomorphine had different profiles of activity. The phencyclidine-like compounds exhibited extremely strong stimulation of the ECoG with very large increases recorded in high frequency (15-50 Hz) activity and reductions in all other frequency bands. Various compounds have been used in an attempt to antagonise the changes in the ECoG. Chlorpromazine caused a slight shift in the dose-response curves as did chlordiazepoxide when used with phencyclidine. The GABA agonists, THIP and muscimol, had no effect on the stimulation of the ECoG. In contrast another presumed GABA agonist, baclofen, proved to be the most effective agent for blocking the stimulation induced by phencyclidine. The role of the GABAB receptor in the action of phencyclidine is discussed.
一种用于持续分析大鼠大脑皮层电图(ECoG)不同频段的自动化技术已被用于量化苯环利定(PCP)和其他各种兴奋剂的作用。已证明苯环利定、依托沙朵和LY154045在各个频段产生相似的变化,而苯丙胺和阿扑吗啡具有不同的活性特征。苯环利定样化合物对ECoG表现出极强的刺激作用,高频(15 - 50赫兹)活动记录到非常大的增加,而其他所有频段均降低。已使用各种化合物试图拮抗ECoG的变化。氯丙嗪与苯环利定合用时会使剂量反应曲线略有偏移,氯氮卓也是如此。GABA激动剂THIP和蝇蕈醇对ECoG的刺激没有影响。相比之下,另一种假定的GABA激动剂巴氯芬被证明是阻断苯环利定诱导的刺激的最有效药物。讨论了GABAB受体在苯环利定作用中的作用。