Department of Pharmacology, Institute of Psychiatry and Neurology, 9 Sobieskiego St., PL-02957 Warsaw, Poland.
Eur J Pharmacol. 2012 Jan 15;674(2-3):275-9. doi: 10.1016/j.ejphar.2011.11.001. Epub 2011 Nov 12.
Individuals prone to drug self-administration may be vulnerable not only to a single drug reinforcer but to a variety of drug reinforcers. It has been shown that two thirds of alcoholics regularly use drugs other than ethanol (alcohol). Up to 30% of alcohol-dependent patients report concurrent misuse of cocaine. The aim of the present study was to investigate intravenous cocaine self-administration in selectively bred, alcohol-preferring WHP (Warsaw high-preferring) and non-preferring WLP (Warsaw low-preferring) rats. It was hypothesized that WHPs could be more prone to cocaine self-administration in comparison to WLPs. Rats from both lines were allowed to nose-poke for cocaine infusions (0.33 mg/kg/infusion) under the FR-1, FR-2, and FR-3 schedule of reinforcement. Dose-response curves were assessed with increasing doses of cocaine (0.03, 0.1, 0.33, 1.0mg/kg/infusion). The WHP and WLP rats did not differ in cocaine self-administration. Both groups quickly acquired nose-poke responding for cocaine, presented a similar response profile when the schedule of reinforcement was increased from FR-1 to FR-3, and similar sensitivity to cocaine in the dose-response test. The present results may indicate that the selective breeding of alcohol-preferring WHP and alcohol non-preferring WLP rats did not lead to differences in cocaine's rewarding effects as assessed in the self-administration procedure.
个体易产生药物自我给药行为,不仅对单一药物强化剂敏感,而且对多种药物强化剂敏感。已经表明,三分之二的酗酒者经常使用除乙醇(酒精)以外的其他药物。多达 30%的酒精依赖患者报告同时滥用可卡因。本研究旨在调查选择性繁殖的、嗜酒的 WHP(华沙高嗜酒品系)和非嗜酒的 WLP(华沙低嗜酒品系)大鼠的静脉内可卡因自我给药。假设与 WLP 相比,WHP 可能更容易进行可卡因自我给药。来自这两个谱系的大鼠被允许在 FR-1、FR-2 和 FR-3 强化方案下进行可卡因输注(0.33mg/kg/输注)的鼻触。通过增加可卡因剂量(0.03、0.1、0.33、1.0mg/kg/输注)评估剂量反应曲线。WHP 和 WLP 大鼠在可卡因自我给药方面没有差异。两组大鼠均迅速获得可卡因的鼻触反应,当强化方案从 FR-1 增加到 FR-3 时,呈现出相似的反应模式,并且在剂量反应测试中对可卡因的敏感性相似。目前的结果可能表明,通过选择性繁殖嗜酒的 WHP 和非嗜酒的 WLP 大鼠,并没有导致在自我给药程序中评估可卡因奖赏效应的差异。