Small Keri M, Nunes Eric, Hughley Shannon, Addy Nii A
Department of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States.
Department of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States; Department of Cellular and Molecular Physiology, New Haven, CT 06511, United States; Interdepartmental Neuroscience Program, Yale University, New Haven, CT 06511, United States.
Neurosci Lett. 2016 Mar 11;616:80-5. doi: 10.1016/j.neulet.2016.01.057. Epub 2016 Jan 29.
Cholinergic and dopaminergic mechanisms within the mesolimbic dopamine system are suggested to play a role in the manifestation of depression and anxiety-related disorders. However, despite the fact that cholinergic mechanisms in the ventral tegmental area (VTA) highly regulate dopamine activity, the role of VTA cholinergic mechanisms in depression-related behaviors is relatively unknown. Here we sought to determine whether enhancing cholinergic tone in the VTA would alter depression and anxiety-related behavior in the forced swim test (FST), elevated plus maze (EPM) and sucrose preference test (SPT). Adult Sprague Dawley male rats received VTA infusion of the acetylcholinesterase inhibitor, physostigmine (0, 1, 2μg/side), immediately prior to the FST, EPM, or SPT. Physostigmine administration increased immobility time in the FST, decreased time spent on open arms in the EPM, and decreased sucrose preference. We also examined whether activation of VTA muscarinic receptors was sufficient to alter behavior in the FST and EPM. Similar to physostigmine, VTA infusion of the muscarinic receptor agonist, pilocarpine (0, 3, 30μg/side), increased immobility time in the FST and decreased time spent on open arms in the EPM. These data suggest that enhanced VTA cholinergic tone promotes pro-depressive and anxiogenic-like effects and demonstrate that specific activation of VTA muscarinic receptors is also sufficient to induce pro-depressive and anxiogenic responses. Together, these findings reveal a novel role of VTA cholinergic, and specifically muscarinic receptor, mechanisms in mediating responses to stress and anxiety.
中脑边缘多巴胺系统中的胆碱能和多巴胺能机制被认为在抑郁症和焦虑相关障碍的表现中起作用。然而,尽管腹侧被盖区(VTA)的胆碱能机制高度调节多巴胺活性,但VTA胆碱能机制在抑郁相关行为中的作用相对未知。在这里,我们试图确定增强VTA中的胆碱能张力是否会改变强迫游泳试验(FST)、高架十字迷宫(EPM)和蔗糖偏好试验(SPT)中的抑郁和焦虑相关行为。成年Sprague Dawley雄性大鼠在FST、EPM或SPT之前,立即接受VTA注射乙酰胆碱酯酶抑制剂毒扁豆碱(0、1、2μg/侧)。给予毒扁豆碱增加了FST中的不动时间,减少了EPM中在开放臂上花费的时间,并降低了蔗糖偏好。我们还研究了VTA毒蕈碱受体的激活是否足以改变FST和EPM中的行为。与毒扁豆碱类似,VTA注射毒蕈碱受体激动剂毛果芸香碱(0、3、30μg/侧)增加了FST中的不动时间,并减少了EPM中在开放臂上花费的时间。这些数据表明,增强的VTA胆碱能张力促进了促抑郁和促焦虑样效应,并表明VTA毒蕈碱受体的特异性激活也足以诱导促抑郁和促焦虑反应。总之,这些发现揭示了VTA胆碱能,特别是毒蕈碱受体机制在介导对压力和焦虑反应中的新作用。