Zapata Agustin, Hwang Eun-Kyung, Lupica Carl R
Electrophysiology Research Section, Cellular Neurobiology Branch, National Institutes of Health, National Institute on Drug Abuse, Intramural Research Program, Baltimore, MD, USA.
Neuropsychopharmacology. 2017 Apr;42(5):1103-1112. doi: 10.1038/npp.2016.286. Epub 2016 Dec 27.
The lateral habenula (LHb) is a brain structure receiving inputs from limbic forebrain areas and innervating major midbrain monoaminergic nuclei. Evidence indicates LHb involvement in sleep control, reward-based decision making, avoidance of punishment, and responses to stress. Additional work has established that the LHb mediates negative feedback in response to aversive events. As a hallmark of drug addiction is the inability to limit drug use despite negative consequences, we hypothesize that LHb dysfunction may have a role in the lack of control over drug seeking. Here we examine the effects of LHb inactivation in control over drug seeking in several cocaine self-administration (SA) paradigms in rats. We find that inhibition of the LHb with GABAergic agonists did not alter cocaine SA under progressive ratio or seeking/taking chained reinforcement schedules, or during punishment-induced suppression of cocaine-reinforced responding. In contrast, LHb inhibition increased cocaine seeking when the drug was not available in rats trained to discriminate its presence using an environmental cue. This effect of LHb inhibition was selective for cocaine, as it did not impair responding for sucrose reinforcement. The effect of LHb injection of GABA agonists was mimicked by intra-LHb muscarinic cholinergic (mACh) antagonist injection, and activation of mACh receptors excited a majority of LHb neurons in in vitro electrophysiology experiments. These results indicate that the LHb participates in the suppression of impulsive responding for cocaine through the activation of a cholinergic circuit, and they suggest that LHb dysfunction may contribute to impaired impulse control associated with drug addiction.
外侧缰核(LHb)是一种脑结构,接收来自边缘前脑区域的输入并支配中脑主要单胺能核团。有证据表明LHb参与睡眠控制、基于奖励的决策、避免惩罚以及对压力的反应。进一步的研究证实,LHb介导对厌恶事件的负反馈。由于药物成瘾的一个标志是尽管有负面后果仍无法限制药物使用,我们推测LHb功能障碍可能在对觅药行为缺乏控制中起作用。在此,我们研究了在几种大鼠可卡因自我给药(SA)范式中,LHb失活对觅药行为控制的影响。我们发现,在渐进比率或寻求/获取链式强化程序下,或在惩罚诱导的可卡因强化反应抑制期间,用GABA能激动剂抑制LHb不会改变可卡因SA。相反,在经过训练利用环境线索辨别可卡因存在的大鼠中,当药物不可用时,LHb抑制会增加可卡因觅求行为。LHb抑制的这种作用对可卡因具有选择性,因为它不会损害对蔗糖强化物的反应。向LHb注射GABA激动剂的效果可被向LHb内注射毒蕈碱胆碱能(mACh)拮抗剂所模拟,并且在体外电生理实验中,激活mACh受体会使大多数LHb神经元兴奋。这些结果表明,LHb通过激活胆碱能回路参与抑制对可卡因的冲动反应,并且提示LHb功能障碍可能导致与药物成瘾相关的冲动控制受损。