Matzeu Alessandra, Martin-Fardon Rémi
Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States.
Front Behav Neurosci. 2021 Feb 23;15:620868. doi: 10.3389/fnbeh.2021.620868. eCollection 2021.
Hypothalamic orexin (Orx) projections to the paraventricular nucleus of the thalamus (PVT) have received growing interest because of their role in drug-seeking behavior. Using an established model of cocaine dependence (i.e., long access [LgA] to cocaine), we previously showed that OrxA injections in the posterior PVT (pPVT) reinstated extinguished cocaine-seeking behavior in rats after an intermediate period of abstinence (2-3 weeks). Considering the long-lasting nature of drug-seeking behavior, the present study examined whether the priming effect of intra-pPVT OrxA administration was preserved after a period of protracted abstinence (4-5 weeks) in rats that self-administered cocaine under LgA conditions. Furthermore, to better understand whether a history of cocaine dependence affects the Orx system-particularly the hypothalamic Orx↔pPVT connection-the number of Orx-expressing cells in the lateral hypothalamus (LH), dorsomedial hypothalamus (DMH), and perifornical area (PFA) and number of orexin receptor 1 (OrxR1)- and OrxR2-expressing cells in the pPVT were quantified. Orexin A administration in the pPVT induced cocaine-seeking behavior after intermediate abstinence, as reported previously. At protracted abstinence, however, the priming effect of OrxA was absent. A higher number of cells that expressed Orx was observed in the LH/DMH/PFA at both intermediate and protracted abstinence. In the pPVT, the number of OrxR2-expressing cells was significantly higher only at intermediate abstinence, with no changes in the number of OrxR1-expressing cells. These data build on our previous findings that the hypothalamic Orx↔pPVT connection is strongly recruited shortly after cocaine abstinence and demonstrate that the priming effect of OrxA is not long lasting. Furthermore, these findings suggest that throughout abstinence, the Orx↔pPVT connection undergoes neuroadaptive changes, reflected by alterations of the number of OrxR2-expressing cells in the pPVT.
由于下丘脑食欲素(Orx)向丘脑室旁核(PVT)的投射在觅药行为中所起的作用,其受到了越来越多的关注。利用已建立的可卡因依赖模型(即长时间接触[LgA]可卡因),我们之前发现,在中间禁欲期(2 - 3周)后,向大鼠丘脑室旁核后部(pPVT)注射食欲素A(OrxA)可恢复已消退的可卡因觅药行为。考虑到觅药行为的长期特性,本研究检测了在LgA条件下自我给药可卡因的大鼠经过一段长时间禁欲期(4 - 5周)后,向pPVT内注射OrxA的启动效应是否依然存在。此外,为了更好地理解可卡因依赖史是否会影响食欲素系统,特别是下丘脑Orx与pPVT之间的联系,我们对下丘脑外侧区(LH)、下丘脑背内侧核(DMH)和穹窿周区(PFA)中表达Orx的细胞数量以及pPVT中表达食欲素受体1(OrxR1)和食欲素受体2(OrxR2)的细胞数量进行了定量分析。如先前报道的那样,在中间禁欲期后,向pPVT注射食欲素A可诱导可卡因觅药行为。然而,在长时间禁欲期,OrxA的启动效应消失。在中间禁欲期和长时间禁欲期,LH/DMH/PFA中表达Orx的细胞数量均较多。在pPVT中,仅在中间禁欲期表达OrxR2的细胞数量显著增加,而表达OrxR1的细胞数量没有变化。这些数据基于我们之前的研究结果,即可卡因戒断后不久,下丘脑Orx与pPVT之间的联系会被强烈激活,并表明OrxA的启动效应并非持久。此外,这些研究结果表明,在整个禁欲期,Orx与pPVT之间的联系会发生神经适应性变化,表现为pPVT中表达OrxR2的细胞数量改变。