Shippenberg T S, Heidbreder C
Behavioral Pharmacology and Genetics Section, NIDA Intramural Research Program, Baltimore, MD 21224, USA.
Eur J Pharmacol. 1995 Jun 23;280(1):55-61. doi: 10.1016/0014-2999(95)00185-n.
A conditioned place preference paradigm was used to determine whether: (i) prior exposure to cocaine results in an enhancement of its rewarding effects, and (ii) the delta-opioid receptor antagonist naltrindole can prevent the development of this response. Rats received daily injections of saline or cocaine (10.0 mg/kg i.p.) for 5 days in the colony room. Additional animals received naltrindole (0.03-0.3 mg/kg s.c.), lithium chloride (20 mg/kg s.c.) or vehicle prior to i.p. injections. Conditioning sessions (2 drug; 2 vehicle) commenced 3 days later. Cocaine (1.0-10.0 mg/kg) was ineffective as a conditioning stimulus in saline pre-exposed rats. In cocaine pre-exposed animals, however, doses of 5.0 and 10.0 mg/kg cocaine resulted in significant drug-induced place preferences. Significant cocaine-induced place preferences were also observed in animals which had received lithium chloride with the cocaine treatment regimen. In animals which had received naltrindole together with the chronic cocaine treatment regimen, cocaine failed to produce a conditioned response. These data demonstrate that the repeated administration of cocaine results in an enhancement of its rewarding effects (e.g. sensitization) and that this phenomenon is prevented by a delta-opioid receptor antagonist. Furthermore, the finding that naltrindole does not modify the acute rewarding effects of cocaine suggests a specific role of delta-opioid receptors in the sensitization process.
(i)先前接触可卡因是否会增强其奖赏效应,以及(ii)δ-阿片受体拮抗剂纳曲吲哚是否能阻止这种反应的形成。大鼠在饲养室中每天接受生理盐水或可卡因(10.0毫克/千克,腹腔注射)注射,持续5天。另外的动物在腹腔注射前接受纳曲吲哚(0.03 - 0.3毫克/千克,皮下注射)、氯化锂(20毫克/千克,皮下注射)或赋形剂。3天后开始条件化训练(2次注射药物;2次注射赋形剂)。可卡因(1.0 - 10.0毫克/千克)对预先用生理盐水处理的大鼠作为条件刺激无效。然而,在预先接触可卡因的动物中,5.0和10.0毫克/千克剂量的可卡因导致了显著的药物诱导的位置偏爱。在接受氯化锂与可卡因治疗方案的动物中也观察到了显著的可卡因诱导的位置偏爱。在接受纳曲吲哚与慢性可卡因治疗方案的动物中,可卡因未能产生条件反应。这些数据表明,重复给予可卡因会增强其奖赏效应(如敏化),并且这种现象可被δ-阿片受体拮抗剂阻止。此外,纳曲吲哚不改变可卡因急性奖赏效应的这一发现表明δ-阿片受体在敏化过程中具有特定作用。