Oades Robert D
Biopsychology Group, Clinic for Child and Adolescent Psychiatry and Psychotherapy, University of Duisburg-Essen, 45147 Essen, Germany.
Prog Brain Res. 2008;172:543-65. doi: 10.1016/S0079-6123(08)00926-6.
Poor control of attention-related and motor processes, often associated with behavioural or cognitive impulsivity, are typical features of children and adults with attention-deficit hyperactivity disorder (ADHD). Until recently clinicians have observed little need to improve on or add to the catecholaminergic model for explaining the features of ADHD. Recent genetic and neuroimaging studies however provide evidence for separate contributions of altered dopamine (DA) and serotonin (5-HT) function in this disorder. Genetic studies imply that for both DA and 5-HT systems variants may frequently occur in ADHD for neurotransmitter uptake, synthesis and breakdown functions. The separate distributions in the brain of mesolimbic DA transporter and mesocortical DA D4 binding sites, both strongly implicated in ADHD, draws attention to potentially differential contributions from the 5-HT system. However, the evidence here points less towards an anatomical differentiation, as towards one in terms of inhibitory/facilitatory pre/post-synaptic location of receptors in the 5-HT(1) and 5-HT(2) families. While the monoamine metabolite levels excreted in ADHD are often correlated, this may well flow from a starting point where 5-HT activity is anomalously higher or lower than the generally lower than normal levels for DA. It appears that perhaps both situations may arise reflecting different diagnostic subgroups of ADHD, and where impulsive characteristics of the subjects reflect externalizing behaviour or cognitive impulsivity. For these features there is clear evidence that DA and 5-HT neuronal systems can and do interact anomalously in ADHD at the level of the soma, the terminals and at a distance. Interactions mediated by macroglia are also likely. However, it remains difficult to ascribe specific mechanisms to their effects (in potentially different subgroups of patients) from this relatively new field of study that has as yet produced rather heterogeneous results.
注意力相关及运动过程控制不佳,常与行为或认知冲动相关,是注意缺陷多动障碍(ADHD)儿童和成人的典型特征。直到最近,临床医生一直认为,在解释ADHD的特征方面,几乎没有必要改进或补充儿茶酚胺能模型。然而,最近的基因和神经影像学研究为多巴胺(DA)和5-羟色胺(5-HT)功能改变在该疾病中的单独作用提供了证据。基因研究表明,对于DA和5-HT系统,神经递质摄取、合成和分解功能的变体可能在ADHD中频繁出现。中脑边缘DA转运体和中脑皮质DA D4结合位点在大脑中的不同分布,两者都与ADHD密切相关,这引起了人们对5-HT系统潜在不同作用的关注。然而,这里的证据与其说是指向解剖学上的差异,不如说是指向5-HT(1)和5-HT(2)家族受体在突触前/后抑制/促进位置方面的差异。虽然ADHD中排泄的单胺代谢物水平通常相互关联,但这很可能源于一个起点,即5-HT活性异常高于或低于通常低于正常水平的DA。似乎这两种情况都可能出现,反映了ADHD的不同诊断亚组,以及受试者的冲动特征反映的是外化行为还是认知冲动。对于这些特征,有明确的证据表明,DA和5-HT神经元系统在ADHD中,在躯体、终末以及远距离水平上能够且确实异常相互作用。由神经胶质细胞介导的相互作用也很可能存在。然而,从这个相对较新的研究领域(其结果相当异质)中,仍难以将特定机制归因于它们的作用(在潜在的不同患者亚组中)。