White I M, Christensen J R, Flory G S, Miller D W, Rebec G V
Department of Psychology, Indiana University, Bloomington 47405, USA.
Psychopharmacology (Berl). 1995 Apr;118(3):324-31. doi: 10.1007/BF02245962.
A lever-release version of the conditioned avoidance response (CAR) task was used to assess the behavioral effects of several psychomotor stimulants in rats. The indirect dopamine agonists, d-amphetamine (0.1 and 0.25 mg/kg) and cocaine (7.5 and 15 mg/kg), enhanced performance on this task. Both drugs increased percent avoidance responses and decreased avoidance latency. A higher dose of amphetamine (0.5 mg/kg) also decreased avoidance latency but failed to improve percent avoidance. Similar effects were seen at low (0.01 and 0.025 mg/kg) and high (0.05 mg/kg) doses of dizocilpine (MK-801), a stimulant that acts as a noncompetitive antagonist of N-methyl-d-aspartate (NMDA) glutamate receptors. When combined with haloperidol (0.1 mg/kg), a dopamine antagonist, amphetamine (0.25 mg/kg) and dizocilpine (0.025 mg/kg) had differential effects on the lever-release CAR task. Thus, amphetamine-haloperidol was significantly better than haloperidol alone on percent avoidance but not on avoidance latency, whereas dizocilpine-haloperidol had the opposite effect: significantly better than haloperidol alone on avoidance latency but not on percent avoidance. Taken together, these results provide further support for dopaminergic mechanisms in CAR performance but suggest an opposing glutamatergic influence.
采用条件性回避反应(CAR)任务的杠杆释放版本来评估几种精神运动兴奋剂对大鼠的行为影响。间接多巴胺激动剂d-苯丙胺(0.1和0.25毫克/千克)和可卡因(7.5和15毫克/千克)可增强大鼠在此任务中的表现。两种药物均增加了回避反应百分比并缩短了回避潜伏期。更高剂量的苯丙胺(0.5毫克/千克)也缩短了回避潜伏期,但未能提高回避反应百分比。作为N-甲基-D-天冬氨酸(NMDA)谷氨酸受体的非竞争性拮抗剂的兴奋剂地佐环平(MK-801),在低剂量(0.01和0.025毫克/千克)和高剂量(0.05毫克/千克)时也出现了类似效果。当与多巴胺拮抗剂氟哌啶醇(0.1毫克/千克)合用时,苯丙胺(0.25毫克/千克)和地佐环平(0.025毫克/千克)对杠杆释放CAR任务产生了不同影响。因此,苯丙胺 - 氟哌啶醇在回避反应百分比上显著优于单独使用氟哌啶醇,但在回避潜伏期上并非如此,而地佐环平 - 氟哌啶醇则产生相反的效果:在回避潜伏期上显著优于单独使用氟哌啶醇,但在回避反应百分比上并非如此。综上所述,这些结果为CAR表现中的多巴胺能机制提供了进一步支持,但也表明了谷氨酸能的相反影响。