Cunningham Christopher L, Gremel Christina M
Department of Behavioral Neuroscience and Portland Alcohol Research Center, Oregon Health and Science University, Portland, OR 97239-3098, USA.
Pharmacol Biochem Behav. 2006 Nov;85(3):612-9. doi: 10.1016/j.pbb.2006.10.016. Epub 2006 Dec 4.
Neurobiological mechanisms underlying rewarding and aversive effects of drugs are often studied by examining effects of various pretreatments on acquisition of conditioned place preference (CPP) or conditioned place aversion (CPA). However, few studies have looked at effects of pretreatment with the same drug used during conditioning. Such studies might offer insight into agonist actions on conditioning while also mimicking real world contingencies experienced by drug users. Previous work from our laboratory, which showed that same drug pre-exposure interfered with acquisition of ethanol CPA but not CPP, was limited by the use of only one pre-treatment time interval (65 min). Thus, the present studies were designed to study other intervals (-5, -15, -30). Pretreatment of DBA/2J mice with ethanol (2 g/kg) reduced the activity response normally evoked by the conditioning dose (2 g/kg) at all pretreatment times, but acquisition of CPP was disrupted only by pretreatment at -5 min. The overall pattern of findings suggests that ethanol's early pharmacological effects interfered with learning the association between the conditioned stimulus (CS) and ethanol 5 min later. Thus, one would expect ethanol agonists, when administered in close proximity to CS-ethanol pairings, to interfere with control of ethanol seeking by that CS.
药物奖赏和厌恶效应背后的神经生物学机制通常通过研究各种预处理对条件性位置偏爱(CPP)或条件性位置厌恶(CPA)习得的影响来进行探究。然而,很少有研究关注在条件化过程中使用相同药物进行预处理的效果。此类研究可能有助于深入了解激动剂对条件化的作用,同时也能模拟吸毒者在现实世界中所经历的情况。我们实验室之前的研究表明,相同药物的预先暴露会干扰乙醇CPA的习得,但不会干扰CPP的习得,不过该研究仅使用了一个预处理时间间隔(65分钟),存在一定局限性。因此,本研究旨在探究其他时间间隔(-5、-15、-30分钟)的情况。用乙醇(2克/千克)对DBA/2J小鼠进行预处理,在所有预处理时间点,均降低了通常由条件化剂量(2克/千克)诱发的活动反应,但只有在-5分钟进行预处理时才会破坏CPP的习得。研究结果的总体模式表明,乙醇的早期药理作用干扰了5分钟后对条件刺激(CS)与乙醇之间关联的学习。因此,可以预期,当乙醇激动剂在接近CS-乙醇配对时给药,会干扰该CS对乙醇寻求行为的控制。