Adams J U, Careri J M, Efferen T R, Rotrosen J
Department of Psychiatry, New York University School of Medicine, Research Service, New York Harbor VA Health Care System, New York 10010, USA.
Behav Pharmacol. 2001 Dec;12(8):603-11. doi: 10.1097/00008877-200112000-00004.
Neuronal substrates that mediate the conditioned effects of cocaine have not been well characterized. To examine dopaminergic mechanisms, three antagonists were tested for their capacity to inhibit the expression of conditioned locomotor activity and conditioned place preference in rats. Antagonists were also assessed against acute cocaine-stimulated locomotor activity for comparison. For locomotor activity conditioning, six conditioning sessions were conducted over a 10-day period. Paired rats received 10 mg/kg cocaine prior to activity sessions and saline after; unpaired controls received saline prior and cocaine after. For place preference conditioning, eight conditioning sessions were conducted over a 13-day period; rats received 10 mg/kg cocaine while restricted to one of two distinct chambers and, on alternate days, they received saline in the other. Antagonists (haloperidol, raclopride and SCH23390; 0.03-0.1 mg/kg) were given only on test days for conditioned effects. All three antagonists significantly and dose-dependently attenuated the direct stimulatory effect of cocaine. SCH23390 showed a tendency to reduce the expression of conditioned locomotor activity, and only haloperidol blocked the expression of conditioned place preference. Thus, direct and conditioned stimulant effects of cocaine were shown to be differentially sensitive to dopamine receptor blockade. Further, conditioned stimulant effects differed from conditioned reinforcing effects in this regard.
介导可卡因条件作用的神经元底物尚未得到充分表征。为了研究多巴胺能机制,测试了三种拮抗剂抑制大鼠条件性运动活动和条件性位置偏爱表达的能力。还评估了这些拮抗剂对急性可卡因刺激的运动活动的作用以作比较。对于运动活动条件反射,在10天内进行了6次条件反射训练。配对的大鼠在活动训练前接受10mg/kg可卡因,之后接受生理盐水;未配对的对照组先接受生理盐水,后接受可卡因。对于位置偏爱条件反射,在13天内进行了8次条件反射训练;大鼠被限制在两个不同的小室之一时接受10mg/kg可卡因,隔天在另一个小室接受生理盐水。拮抗剂(氟哌啶醇、雷氯必利和SCH23390;0.03 - 0.1mg/kg)仅在测试日给予以观察条件作用效果。所有三种拮抗剂均显著且剂量依赖性地减弱了可卡因的直接刺激作用。SCH23390有降低条件性运动活动表达的趋势,只有氟哌啶醇阻断了条件性位置偏爱的表达。因此,可卡因的直接和条件性刺激作用对多巴胺受体阻断表现出不同的敏感性。此外,在这方面条件性刺激作用与条件性强化作用有所不同。