Deakin J F W
Neuroscience and Psychiatry Unit, University of Manchester, United Kingdom.
J Neural Transm Suppl. 2003(64):79-93. doi: 10.1007/978-3-7091-6020-6_5.
Impaired 5HT functioning has been implicated in two very different psychiatric syndromes: antisocial personality disorder and depression. In both, reduced csf concentration of 5HIAA and blunted circulating hormone responses to 5HT drug challenge have been described. The paradox can be resolved by the theory that the two main ascending 5HT pathways mediate adaptive responses to future and current adversity. Projections of the anterior group of raphe 5HT cells (dorsal raphe nucleus) oppose the action of dopamine and mediate avoidance of threats. Impaired function sensitises the dopamine system resulting in impulsivity and drug addiction. Posterior 5HT cells (median raphe nucleus) innervate hippocampus and cingulate gyrus and suppress memory and awareness of current and past adversity. Impaired function results in low mood, low self-esteem, hopelessness and pessimism. Modern imaging methods are providing startling corroboration of these ideas.
5-羟色胺(5HT)功能受损与两种截然不同的精神综合征有关:反社会人格障碍和抑郁症。在这两种病症中,均有脑脊液中5-羟吲哚乙酸(5HIAA)浓度降低以及对5HT药物激发的循环激素反应迟钝的描述。这一矛盾可以通过以下理论来解释:两条主要的5HT上行通路介导对未来和当前逆境的适应性反应。中缝5HT细胞前组(背侧中缝核)的投射与多巴胺的作用相反,并介导对威胁的回避。功能受损会使多巴胺系统敏感化,导致冲动和药物成瘾。后5HT细胞(中缝正中核)支配海马体和扣带回,并抑制对当前和过去逆境的记忆及认知。功能受损会导致情绪低落、自卑、绝望和悲观。现代成像方法为这些观点提供了惊人的佐证。