Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520-8035, USA.
Alcohol. 2012 Feb;46(1):17-27. doi: 10.1016/j.alcohol.2011.08.011. Epub 2011 Oct 1.
Research indicates opioid antagonists can reduce alcohol drinking in rodents. However, tests examining the effects of opioid antagonists on ethanol seeking and relapse behavior have been limited. The present study examined the effects of two opioid antagonists on ethanol maintenance, seeking, and relapse responding by alcohol-preferring (P) rats. Adult P rats were self-trained in two-lever operant chambers to self-administer 15% (vol/vol) ethanol on a fixed-ratio 5 (FR5) versus water on a FR1 concurrent schedule of reinforcement in daily 1-h sessions. After 10 weeks, rats underwent extinction training, followed by 2 weeks in their home cages. Rats were then returned to the operant chambers without ethanol or water to measure responses on the ethanol and water levers for four sessions. After a subsequent 2 weeks in the home cage, without access to ethanol, rats were returned to the operant chambers with ethanol and water available. Effects of antagonists on maintenance responding were tested after several weeks of daily 1-h sessions. Naltrexone (NAL; 1-10mg/kg, subcutaneously [s.c.]; n=8/dose), LY255582 (LY; 0.03-1mg/kg, s.c.; n=8/dose), or vehicle were injected 30min before the first session (in the absence of ethanol), following 2 weeks in their home cages, and for four consecutive sessions of ethanol self-administration under maintenance and relapse conditions. Both NAL and LY reduced responses on the ethanol lever without any fluids present, and ethanol self-administration under relapse and on-going drinking conditions, with LY being more potent than NAL. Both NAL and LY were less effective in reducing responding in the absence of ethanol than in reducing ethanol self-administration. Overall, the results indicate that the opioid system is involved in mediating ethanol seeking, and ethanol self-administration under relapse and on-going alcohol drinking, but that different neurocircuits may underlie these behaviors.
研究表明,阿片受体拮抗剂可以减少啮齿动物的饮酒量。然而,检查阿片受体拮抗剂对乙醇寻求和复发性行为影响的测试受到限制。本研究通过酒精偏好(P)大鼠检查了两种阿片受体拮抗剂对乙醇维持、寻求和复发性反应的影响。成年 P 大鼠在双杠操作室中自我训练,以在 FR5 固定比率与 FR1 同时强化方案下自我给予 15%(体积/体积)乙醇,每天 1 小时。经过 10 周的训练后,大鼠进行了消退训练,然后在其自己的笼子中进行了 2 周。然后,大鼠返回操作室,没有乙醇或水,以测量四个疗程的乙醇和水杠杆的反应。在随后的 2 周没有在笼子里接触乙醇后,大鼠被返回操作室,同时提供乙醇和水。在经过几周的每日 1 小时的训练后,测试了拮抗剂对维持反应的影响。纳曲酮(NAL;1-10mg/kg,皮下[sc];n=8/剂量),LY255582(LY;0.03-1mg/kg,sc;n=8/剂量)或载体在第一次注射前 30 分钟(无乙醇),在其笼中进行 2 周,以及在维持和复发条件下连续 4 次乙醇自我给药的情况下进行注射。NAL 和 LY 均减少了无任何液体存在时对乙醇杠杆的反应,并且在复发和持续饮酒条件下减少了乙醇自我给药,而 LY 比 NAL 更有效。NAL 和 LY 在没有乙醇的情况下降低反应的效果不如在减少乙醇自我给药时有效。总的来说,这些结果表明,阿片系统参与调节乙醇寻求,以及在复发和持续饮酒条件下的乙醇自我给药,但不同的神经回路可能是这些行为的基础。