Williams Mark J, Adinoff Bryon
Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390-8564, USA.
Neuropsychopharmacology. 2008 Jul;33(8):1779-97. doi: 10.1038/sj.npp.1301585. Epub 2007 Oct 10.
Central nervous system cholinergic neurons arise from several discrete sources, project to multiple brain regions, and exert specific effects on reward, learning, and memory. These processes are critical for the development and persistence of addictive disorders. Although other neurotransmitters, including dopamine, glutamate, and serotonin, have been the primary focus of drug research to date, a growing preclinical literature reveals a critical role of acetylcholine (ACh) in the experience and progression of drug use. This review will present and integrate the findings regarding the role of ACh in drug dependence, with a primary focus on cocaine and the muscarinic ACh system. Mesostriatal ACh appears to mediate reinforcement through its effect on reward, satiation, and aversion, and chronic cocaine administration produces neuroadaptive changes in the striatum. ACh is further involved in the acquisition of conditional associations that underlie cocaine self-administration and context-dependent sensitization, the acquisition of associations in conditioned learning, and drug procurement through its effects on arousal and attention. Long-term cocaine use may induce neuronal alterations in the brain that affect the ACh system and impair executive function, possibly contributing to the disruptions in decision making that characterize this population. These primarily preclinical studies suggest that ACh exerts a myriad of effects on the addictive process and that persistent changes to the ACh system following chronic drug use may exacerbate the risk of relapse during recovery. Ultimately, ACh modulation may be a potential target for pharmacological treatment interventions in cocaine-addicted subjects. However, the complicated neurocircuitry of the cholinergic system, the multiple ACh receptor subtypes, the confluence of excitatory and inhibitory ACh inputs, and the unique properties of the striatal cholinergic interneurons suggest that a precise target of cholinergic manipulation will be required to impact substance use in the clinical population.
中枢神经系统胆碱能神经元起源于几个离散的来源,投射到多个脑区,并对奖赏、学习和记忆产生特定影响。这些过程对于成瘾性障碍的发展和持续存在至关重要。尽管包括多巴胺、谷氨酸和5-羟色胺在内的其他神经递质是迄今为止药物研究的主要焦点,但越来越多的临床前文献揭示了乙酰胆碱(ACh)在药物使用体验和进展中的关键作用。本综述将呈现并整合关于ACh在药物依赖中作用的研究结果,主要关注可卡因和毒蕈碱型ACh系统。中脑纹状体ACh似乎通过其对奖赏、饱腹感和厌恶的影响来介导强化作用,长期给予可卡因会在纹状体中产生神经适应性变化。ACh还参与了可卡因自我给药和情境依赖性敏化所基于的条件性联想的习得、条件学习中联想的习得,以及通过其对唤醒和注意力的影响来获取药物。长期使用可卡因可能会导致大脑中的神经元改变,影响ACh系统并损害执行功能,这可能导致该人群决策过程的紊乱。这些主要是临床前研究表明,ACh对成瘾过程产生多种影响,长期药物使用后ACh系统的持续变化可能会增加康复期间复发的风险。最终,ACh调节可能是可卡因成瘾受试者药物治疗干预的潜在靶点。然而,胆碱能系统复杂的神经回路、多种ACh受体亚型、兴奋性和抑制性ACh输入的汇合,以及纹状体胆碱能中间神经元的独特特性表明,需要精确的胆碱能操纵靶点才能影响临床人群的物质使用。