Department of Cellular and Molecular Pharmacology, Rosalind Franklin University of Medicine and Science, The Chicago Medical School, North Chicago, IL 60064, United States.
Prog Neurobiol. 2013 Jan;100:60-80. doi: 10.1016/j.pneurobio.2012.10.001. Epub 2012 Oct 17.
The psychostimulants methylphenidate (Ritalin, Concerta), amphetamine (Adderall), and modafinil (Provigil) are widely used in the treatment of medical conditions such as attention-deficit hyperactivity disorder and narcolepsy and, increasingly, as "cognitive enhancers" by healthy people. The long-term neuronal effects of these drugs, however, are poorly understood. A substantial amount of research over the past two decades has investigated the effects of psychostimulants such as cocaine and amphetamines on gene regulation in the brain because these molecular changes are considered critical for psychostimulant addiction. This work has determined in some detail the neurochemical and cellular mechanisms that mediate psychostimulant-induced gene regulation and has also identified the neuronal systems altered by these drugs. Among the most affected brain systems are corticostriatal circuits, which are part of cortico-basal ganglia-cortical loops that mediate motivated behavior. The neurotransmitters critical for such gene regulation are dopamine in interaction with glutamate, while other neurotransmitters (e.g., serotonin) play modulatory roles. This review presents (1) an overview of the main findings on cocaine- and amphetamine-induced gene regulation in corticostriatal circuits in an effort to provide a cellular framework for (2) an assessment of the molecular changes produced by methylphenidate, medical amphetamine (Adderall), and modafinil. The findings lead to the conclusion that protracted exposure to these cognitive enhancers can induce gene regulation effects in corticostriatal circuits that are qualitatively similar to those of cocaine and other amphetamines. These neuronal changes may contribute to the addiction liability of the psychostimulant cognitive enhancers.
哌甲酯(利他林、专注达)、安非他命(Adderall)和莫达非尼(Provigil)等精神兴奋剂被广泛用于治疗注意力缺陷多动障碍和嗜睡症等医疗状况,并且越来越多地被健康人群用作“认知增强剂”。然而,这些药物的长期神经元效应知之甚少。在过去的二十年中,大量研究调查了可卡因和安非他命等精神兴奋剂对大脑基因调控的影响,因为这些分子变化被认为是精神兴奋剂成瘾的关键。这项工作详细确定了介导精神兴奋剂诱导基因调控的神经化学和细胞机制,并确定了这些药物改变的神经元系统。受影响最严重的大脑系统之一是皮质纹状体回路,它是介导动机行为的皮质基底神经节-皮质回路的一部分。对于这种基因调控至关重要的神经递质是多巴胺与谷氨酸相互作用,而其他神经递质(如血清素)则起调节作用。这篇综述介绍了(1)可卡因和安非他命在皮质纹状体回路中诱导基因调控的主要发现,以努力为(2)评估哌甲酯、医学用安非他命(Adderall)和莫达非尼引起的分子变化提供一个细胞框架。研究结果得出的结论是,长时间暴露于这些认知增强剂会在皮质纹状体回路中诱导基因调控效应,其性质与可卡因和其他安非他命相似。这些神经元变化可能导致这些精神兴奋剂认知增强剂的成瘾倾向。