Young Richard, Bondareva Tatiana, Wesolowska Anna, Glennon Richard A
Department of Medicinal Chemistry, School of Pharmacy, Medical College of Virginia, Box 980540, Virginia Commonwealth University, Richmond, 23298-0540, USA.
Pharmacol Biochem Behav. 2006 Apr;83(4):612-7. doi: 10.1016/j.pbb.2006.03.025. Epub 2006 May 3.
It is well established that the discriminative stimulus (DS) effect of amphetamine involves a dopaminergic and/or noradrenergic mechanism. These catecholamines can be modulated by the 5-HT(1A) serotonin receptor agonist 8-hydroxy-2-(N,N-di-n-propylamino)tetralin (8-OH DPAT). The present study was conducted to determine whether 8-OH DPAT could influence the DS effects of (+)amphetamine. Administration of 8-OH DPAT doses to Sprague-Dawley rats trained to discriminate 1 mg/kg of (+)amphetamine (ED(50)=0.33 mg/kg) using a two-lever operant paradigm (VI-15 s schedule of reinforcement for appetitive reward) failed to result in stimulus generalization when administered alone, and failed to antagonize the stimulus effect when administered in combination with the training dose of (+)amphetamine. However, administration of 8-OH DPAT doses that produced saline-like responding (i.e., 0.01-0.1 mg/kg; <20% amphetamine-appropriate responding) in combination with the ED(50) dose of (+)amphetamine resulted in the animals' making a progressively greater number of responses on the drug-appropriate lever such that a combination of 0.1 mg/kg of 8-OH DPAT plus (+)amphetamine (0.33 mg/kg) elicited 91% (+)amphetamine-appropriate responding. In a separate study, administration of (+)amphetamine doses in combination with fixed doses of 8-OH DPAT (either 0.01 or 0.1 mg/kg) resulted in an apparent leftward shift of the dose-response curve. The results indicate that (+)amphetamine can be more effective as a discriminative stimulus in the presence of 8-OH DPAT than in its absence.
苯丙胺的辨别性刺激(DS)效应涉及多巴胺能和/或去甲肾上腺素能机制,这一点已得到充分证实。这些儿茶酚胺可被5-HT(1A) 5-羟色胺受体激动剂8-羟基-2-(N,N-二正丙基氨基)四氢萘(8-OH DPAT)调节。本研究旨在确定8-OH DPAT是否会影响(+)苯丙胺的DS效应。对经训练使用双杠杆操作范式(以15秒可变间隔强化程序获取食欲奖励)来辨别1mg/kg(+)苯丙胺(半数有效剂量[ED(50)] = 0.33mg/kg)的斯普拉格-道利大鼠给予不同剂量的8-OH DPAT,单独给药时未产生刺激泛化,与训练剂量的(+)苯丙胺联合给药时也未拮抗刺激效应。然而,给予能产生类似生理盐水反应剂量的8-OH DPAT(即0.01 - 0.1mg/kg;苯丙胺适应性反应低于20%)并联合(+)苯丙胺的ED(50)剂量,结果导致动物在药物适应性杠杆上做出的反应数量逐渐增加,使得0.1mg/kg的8-OH DPAT与(+)苯丙胺(0.33mg/kg)联合给药时引发了91%的(+)苯丙胺适应性反应。在另一项研究中,给予(+)苯丙胺剂量并联合固定剂量的8-OH DPAT(0.01mg/kg或0.1mg/kg),导致剂量反应曲线明显左移。结果表明,与不存在8-OH DPAT时相比,(+)苯丙胺在有8-OH DPAT存在时作为辨别性刺激可能更有效。