Doly Stéphane, Quentin Emily, Eddine Raphaël, Tolu Stefania, Fernandez Sebastian P, Bertran-Gonzalez Jesus, Valjent Emmanuel, Belmer Arnauld, Viñals Xavier, Callebert Jacques, Faure Philippe, Meye Frank J, Hervé Denis, Robledo Patricia, Mameli Manuel, Launay Jean-Marie, Maldonado Rafael, Maroteaux Luc
Institut national de la santé et de la recherche médicale, Unité Mixte de Recherche-S839, F-75005 Paris, France.
Sorbonne Universités, Universite Pierre et Marie Curie (Paris VI), Unité Mixte de Recherche-S839, F-75005 Paris, France.
J Neurosci. 2017 Oct 25;37(43):10372-10388. doi: 10.1523/JNEUROSCI.1354-17.2017. Epub 2017 Sep 21.
Addiction is a maladaptive pattern of behavior following repeated use of reinforcing drugs in predisposed individuals, leading to lifelong changes. Common among these changes are alterations of neurons releasing dopamine in the ventral and dorsal territories of the striatum. The serotonin 5-HT receptor has been involved in various behaviors, including impulsivity, response to antidepressants, and response to psychostimulants, pointing toward putative interactions with the dopamine system. Despite these findings, it remains unknown whether 5-HT receptors directly modulate dopaminergic activity and the possible mechanisms involved. To answer these questions, we investigated the contribution of 5-HT receptors to cocaine-dependent behavioral responses. Male mice permanently lacking 5-HT receptors, even restricted to dopamine neurons, developed heightened cocaine-induced locomotor responses. Retrograde tracing combined with single-cell mRNA amplification indicated that 5-HT receptors are expressed by mesolimbic dopamine neurons. and electrophysiological recordings showed that 5-HT-receptor inactivation in dopamine neurons affects their neuronal activity and increases AMPA-mediated over NMDA-mediated excitatory synaptic currents. These changes are associated with lower ventral striatum dopamine activity and blunted cocaine self-administration. These data identify the 5-HT receptor as a pharmacological intermediate and provide mechanistic insight into attenuated dopamine tone following exposure to drugs of abuse. Here we report that mice lacking 5-HT receptors totally or exclusively in dopamine neurons exhibit heightened cocaine-induced locomotor responses. Despite the sensitized state of these mice, we found that associated changes include lower ventral striatum dopamine activity and lower cocaine operant self-administration. We described the selective expression of 5-HT receptors in a subpopulation of dopamine neurons sending axons to the ventral striatum. Increased bursting properties of these dopamine neurons and a concomitant increase in AMPA synaptic transmission to dopamine neurons were found in mice lacking 5-HT receptors. These data support the idea that the chronic 5-HT-receptor inhibition makes mice behave like animals already exposed to cocaine with higher cocaine-induced locomotion associated with changes in dopamine neuron reactivity.
成瘾是易感个体反复使用强化药物后出现的适应不良行为模式,会导致终身改变。这些改变中常见的是纹状体腹侧和背侧区域释放多巴胺的神经元发生改变。5-羟色胺(5-HT)受体参与了多种行为,包括冲动性、对抗抑郁药的反应以及对精神兴奋剂的反应,这表明其与多巴胺系统可能存在相互作用。尽管有这些发现,但5-HT受体是否直接调节多巴胺能活性以及其中涉及的可能机制仍不清楚。为了回答这些问题,我们研究了5-HT受体对可卡因依赖行为反应的作用。永久性缺乏5-HT受体的雄性小鼠,即使仅限于多巴胺能神经元,也会出现增强的可卡因诱导的运动反应。逆行追踪结合单细胞mRNA扩增表明,中脑边缘多巴胺能神经元表达5-HT受体。电生理记录显示,多巴胺能神经元中5-HT受体失活会影响其神经元活动,并增加α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)介导的兴奋性突触电流,而不是N-甲基-D-天冬氨酸(NMDA)介导的。这些变化与腹侧纹状体多巴胺活性降低和可卡因自我给药减弱有关。这些数据确定5-HT受体为一种药理学中介,并为滥用药物后多巴胺张力减弱提供了机制性见解。在此我们报告,完全或仅在多巴胺能神经元中缺乏5-HT受体的小鼠表现出增强的可卡因诱导的运动反应。尽管这些小鼠处于敏感状态,但我们发现相关变化包括腹侧纹状体多巴胺活性降低和可卡因操作性自我给药减少。我们描述了5-HT受体在向腹侧纹状体发送轴突的多巴胺能神经元亚群中的选择性表达。在缺乏5-HT受体的小鼠中,发现这些多巴胺能神经元的爆发特性增加,并且AMPA突触传递到多巴胺能神经元的过程也随之增加。这些数据支持这样一种观点,即慢性5-HT受体抑制使小鼠表现得像已经接触过可卡因的动物,更高的可卡因诱导运动与多巴胺能神经元反应性变化有关。