Department of Neuroscience, Medical University of South Carolina, Charleston, SC, 29425.
Salk Institute for Biological Studies, La Jolla, CA 92037.
J Neurosci. 2021 Jan 13;41(2):298-306. doi: 10.1523/JNEUROSCI.0708-20.2020. Epub 2020 Nov 19.
The aversive properties associated with drugs of abuse influence both the development of addiction and relapse. Cocaine produces strong aversive effects after rewarding effects wear off, accompanied by increased firing in the lateral habenula (LHb) that contributes to downstream activation of the rostromedial tegmental nucleus (RMTg). However, the sources of this LHb activation are unknown, as the LHb receives many excitatory inputs whose contributions to cocaine aversion remain uncharacterized. Using cFos activation and electrophysiology in male rats, we demonstrated that the rostral entopeduncular nucleus (rEPN) was the most responsive region to cocaine among LHb afferents examined and that single cocaine infusions induced biphasic responses in rEPN neurons, with inhibition during cocaine's initial rewarding phase transitioning to excitation during cocaine's delayed aversive phase. Furthermore, rEPN lesions reduced cocaine-induced cFos activation by 2-fold in the LHb and by a smaller proportion in the RMTg, while inactivation of the rEPN or the rEPN-LHb pathway attenuated cocaine avoidance behaviors measured by an operant runway task and by conditioned place aversion (CPA). These data show an essential but not exclusive role of rEPN and its projections to the LHb in processing the aversive effects of cocaine, which could serve as a novel target for addiction vulnerability. Cocaine produces well-known rewarding effects but also strong aversive effects that influence addiction propensity, but whose mechanisms are poorly understood. We had previously reported that the lateral habenula (LHb) is activated by cocaine and contributes to cocaine's aversive effects, and the current findings show that the rostral entopeduncular nucleus (rEPN) is a major contributor to this LHb activation and to conditioned avoidance of cocaine. These findings show a critical, though not exclusive, rEPN role in cocaine's aversive effects, and shed light on the development of addiction.
与滥用药物相关的厌恶特性会影响成瘾和复发的发展。可卡因在奖赏效应消退后会产生强烈的厌恶效应,同时 lateral habenula (LHb) 的放电增加,这有助于下游 rostromedial tegmental nucleus (RMTg) 的激活。然而,这种 LHb 激活的来源尚不清楚,因为 LHb 接收许多兴奋性输入,其对可卡因厌恶的贡献仍不清楚。通过雄性大鼠的 cFos 激活和电生理学研究,我们证明了 rostral entopeduncular nucleus (rEPN) 是 LHb 传入纤维中对可卡因反应最敏感的区域,单次可卡因输注会在 rEPN 神经元中产生双相反应,在可卡因最初的奖赏阶段抑制,然后在可卡因延迟的厌恶阶段兴奋。此外,rEPN 损伤使 LHb 中的可卡因诱导的 cFos 激活减少了 2 倍,而在 RMTg 中的减少比例较小,而 rEPN 或 rEPN-LHb 通路的失活则削弱了操作性逃避任务和条件性位置厌恶 (CPA) 测量的可卡因回避行为。这些数据表明,rEPN 及其投射到 LHb 在处理可卡因的厌恶效应中具有重要但不是唯一的作用,这可能成为成瘾易感性的一个新靶点。可卡因产生众所周知的奖赏效应,但也有强烈的厌恶效应,会影响成瘾倾向,但这些机制尚不清楚。我们之前曾报道过 lateral habenula (LHb) 被可卡因激活,并有助于可卡因的厌恶效应,而目前的研究结果表明,rostral entopeduncular nucleus (rEPN) 是这种 LHb 激活和对可卡因条件性回避的主要贡献者。这些发现表明 rEPN 在可卡因的厌恶效应中具有关键作用,但不是唯一作用,并为成瘾的发展提供了线索。