Reid L D, Hubbell C L, Glaccum M B, Bilsky E J, Portoghese P S, Porreca F
Department of Psychology, Renssclaer Polytechnic Institute, Troy, NY 12180.
Life Sci. 1993;52(9):PL67-71. doi: 10.1016/0024-3205(93)90084-g.
Recent experimental results have led to the suggestion that opioid antagonists can modulate the reinforcing properties of cocaine. In this experiment, rats were fixed with chronically indwelling bipolar electrodes for stimulation of the medial forebrain bundle (MFB) as it courses through the hypothalamus. Rats were taught to press a lever for brief trains of electrical stimulation of the MFB. Subsequently, they were allowed to press for varying intensities of stimulation daily until their response rates were stable. Cocaine (5 mg/kg, s.c.) enhanced the rate of pressing for lower intensities of brain stimulation. Naltrindole (3 mg/kg, i.p.) had no effect on response rate alone but blocked the cocaine-induced facilitation of pressing for rewarding brain stimulation. An implication that can be drawn from these data is that naltrindole, or other delta-selective opioid antagonists, might be effective as medicines for use in treating cocaine abuse.
最近的实验结果表明,阿片类拮抗剂可以调节可卡因的强化特性。在本实验中,给大鼠长期植入双极电极,用于刺激穿过下丘脑的内侧前脑束(MFB)。训练大鼠按压杠杆以获得MFB的短暂电刺激序列。随后,让它们每天按压以获得不同强度的刺激,直到其反应率稳定。可卡因(5毫克/千克,皮下注射)提高了对较低强度脑刺激的按压率。纳曲吲哚(3毫克/千克,腹腔注射)单独对反应率没有影响,但阻断了可卡因诱导的对奖励性脑刺激按压的促进作用。从这些数据中可以得出的一个结论是,纳曲吲哚或其他δ-选择性阿片类拮抗剂可能作为治疗可卡因滥用的药物有效。