Human Developmental Neurobiology Unit, Okinawa Institute of Science and Technology Graduate University, Kunigami, Okinawa 904-0412, Japan.
Neurotherapeutics. 2012 Jul;9(3):622-34. doi: 10.1007/s13311-012-0132-y.
Attention deficit hyperactivity disorder (ADHD) presents special challenges for drug development. Current treatment with psychostimulants and nonstimulants is effective, but their mechanism of action beyond the cellular level is incompletely understood. We review evidence suggesting that altered reinforcement mechanisms are a fundamental characteristic of ADHD. We show that a deficit in the transfer of dopamine signals from established positive reinforcers to cues that predict such reinforcers may underlie these altered reinforcement mechanisms, and in turn explain key symptoms of ADHD. We argue that the neural substrates controlling the excitation and inhibition of dopamine neurons during the transfer process are a promising target for future drug development. There is a need to develop animal models and behavioral paradigms that can be used to experimentally investigate these mechanisms and their effects on sensitivity to reinforcement. More specific and selective targeting of drug development may be possible through this approach.
注意缺陷多动障碍(ADHD)在药物开发方面带来了特殊的挑战。目前使用的精神兴奋剂和非兴奋剂治疗方法是有效的,但它们在细胞水平之外的作用机制还不完全清楚。我们回顾了一些证据,这些证据表明,强化机制的改变是 ADHD 的一个基本特征。我们表明,多巴胺信号从已建立的正强化物向预测此类强化物的线索的传递缺陷可能是这些强化机制改变的基础,并反过来解释了 ADHD 的关键症状。我们认为,在传递过程中控制多巴胺神经元兴奋和抑制的神经基质是未来药物开发的一个有前途的目标。需要开发可以用于实验研究这些机制及其对强化敏感性影响的动物模型和行为范式。通过这种方法,药物开发可能会更加具体和有针对性。