De Vries T J, Schoffelmeer A N, Binnekade R, Mulder A H, Vanderschuren L J
Research Institute Neurosciences Vrije Universiteit, Department of Pharmacology, Medical Faculty, Free University, Amsterdam, The Netherlands.
Eur J Neurosci. 1998 Nov;10(11):3565-71. doi: 10.1046/j.1460-9568.1998.00368.x.
The present study was designed to evaluate the relationship between reinstatement of drug-seeking behaviour following long-term extinction of intravenous (i.v.) drug self-administration (an animal model for craving) and long-term behavioural sensitization. Rats were allowed to self-administer heroin (50 microg/kg per inj., 14 daily sessions), cocaine (500 microg/kg per inj., 10 daily sessions) or saline. Following a 3-week extinction period, reinstatement tests were performed to evaluate priming effects of amphetamine, cocaine and heroin on nonreinforced drug-seeking behaviour. In addition, the occurrence of long-term behavioural sensitization in rats with a history of heroin or cocaine self-administration was determined. Heroin-seeking behaviour was reinstated by heroin (0.25 mg/kg), amphetamine (1.0 mg/kg) and cocaine (10 mg/kg). In addition, animals with a history of heroin self-administration displayed locomotor sensitization to both heroin and amphetamine. Cocaine-seeking behaviour was reinstated by cocaine and amphetamine, but not by heroin. Interestingly, locomotor sensitization to amphetamine, but not heroin, was observed in animals with a history of cocaine self-administration. In other words, the induction of drug-seeking behaviour following a prolonged drug-free period was found to be associated with the expression of long-term behavioural sensitization. These data provide experimental evidence for a role of behavioural sensitization in the incentive motivation underlying drug-seeking behaviour. If drug hyperresponsiveness would indeed be a crucial factor in drug-induced craving in human addicts, pharmacological readjustment of the neuroadaptations underlying drug sensitization may prevent relapse to drug use long after detoxification.
本研究旨在评估静脉注射药物自我给药长期消退后(一种渴求的动物模型)复吸觅药行为与长期行为敏化之间的关系。大鼠被允许自我给药海洛因(每次注射50微克/千克,每天14次)、可卡因(每次注射500微克/千克,每天10次)或生理盐水。在3周的消退期后,进行复吸测试以评估苯丙胺、可卡因和海洛因对非强化觅药行为的启动效应。此外,还确定了有海洛因或可卡因自我给药史的大鼠中是否出现长期行为敏化。海洛因(0.25毫克/千克)、苯丙胺(1.0毫克/千克)和可卡因(10毫克/千克)可使觅海洛因行为复现。此外,有海洛因自我给药史的动物对海洛因和苯丙胺均表现出运动敏化。可卡因和苯丙胺可使觅可卡因行为复现,但海洛因不能。有趣的是,有可卡因自我给药史的动物对苯丙胺表现出运动敏化,但对海洛因没有。换句话说,发现长时间无药期后觅药行为的诱导与长期行为敏化的表达有关。这些数据为行为敏化在觅药行为背后的动机性激励中所起的作用提供了实验证据。如果药物高反应性确实是人类成瘾者药物诱导渴求的关键因素,那么对药物敏化背后的神经适应性进行药理学调整可能会在戒毒很久之后预防复吸。