Schaefer G J, Michael R P
Department of Psychiatry, Emory University School of Medicine, Atlanta, GA 30322.
Psychopharmacology (Berl). 1990;102(2):263-8. doi: 10.1007/BF02245931.
Rats were implanted with stimulating electrodes aimed at the medial forebrain bundle-lateral hypothalamus (MFB-LH) and were trained to lever-press for brain self-stimulation on a fixed interval: 60 s schedule of reinforcement. The effects of graded doses of naloxone (0.1-30 mg/kg), morphine (0.3-5.6 mg/kg), naloxone plus morphine, d-amphetamine (0.03-1.0 mg/kg), naloxone plus d-amphetamine, phencyclidine (0.3-5.6 mg/kg), and naloxone plus phencyclidine were tested. Naloxone produced a significant decrease in rates at 30 mg/kg. Naloxone (0.1-1.0 mg/kg) plus morphine blocked the dose-dependent decrease produced by morphine alone. In contrast, naloxone (1.0-10 mg/kg) plus d-amphetamine attenuated the graded increase in response rates produced by d-amphetamine. Naloxone (1.0-10 mg/kg) plus phencyclidine did not reliably change the increase in response rates produced by phencyclidine alone. The use of the fixed interval schedule of brain self-stimulation to study these drug interactions is novel, and further demonstrates that the highly reinforcing aspects of brain stimulation, known to be influenced by dopamine, may also be modulated by the endogenous opiate system.
将刺激电极植入大鼠体内,电极目标为内侧前脑束-外侧下丘脑(MFB-LH),并训练大鼠在固定间隔强化时间表(60秒)下按压杠杆以进行脑自我刺激。测试了不同剂量的纳洛酮(0.1 - 30毫克/千克)、吗啡(0.3 - 5.6毫克/千克)、纳洛酮加吗啡、右旋苯丙胺(0.03 - 1.0毫克/千克)、纳洛酮加右旋苯丙胺、苯环利定(0.3 - 5.6毫克/千克)以及纳洛酮加苯环利定的效果。纳洛酮在30毫克/千克时使速率显著降低。纳洛酮(0.1 - 1.0毫克/千克)加吗啡可阻断单独使用吗啡产生的剂量依赖性降低。相反,纳洛酮(1.0 - 10毫克/千克)加右旋苯丙胺减弱了右旋苯丙胺产生的反应速率的分级增加。纳洛酮(1.0 - 10毫克/千克)加苯环利定未能可靠地改变单独使用苯环利定产生的反应速率增加。使用固定间隔的脑自我刺激时间表来研究这些药物相互作用是新颖的,并且进一步证明已知受多巴胺影响的脑刺激的高度强化方面也可能受内源性阿片系统调节。