Department of Child and Adolescent Psychiatry, University of Technology Dresden, Fetscherstrasse 74, 01307 Dresden, Germany.
Neurosci Biobehav Rev. 2013 Jul;37(6):1069-84. doi: 10.1016/j.neubiorev.2012.10.004. Epub 2012 Oct 17.
Almost since the beginning of research on Tourette syndrome (TS), tics have been linked to a dysfunction of the dopamine (DA) system. At first, this assumption was mainly based on clinical findings of DA antagonists being the most effective drug in treating tics, but in recent years nuclear imaging has enabled a much deeper understanding of DA neurotransmission in TS. Based on the findings of various PET and SPECT studies the first part of the review discusses four hypotheses on DA dysfunctions in TS: (i) DA hyperinnervation, (ii) supersensitive DA receptors, (iii) pre-synaptic DA abnormality and (iv) DA tonic-phasic dysfunction. According to the latter hypothesis, reduced levels of tonic DA in the extracellular space lead to higher concentrations of DA in the axon terminal and an increase of stimulus-dependent DA release. The second part of the review addresses the modulating role of DA in some major clinical features of TS, like the exacerbation with stress or infection and the association with deficient sensorimotor gating.
几乎从研究妥瑞氏症(TS)开始,人们就认为抽搐与多巴胺(DA)系统功能障碍有关。起初,这种假设主要基于临床发现,即 DA 拮抗剂是治疗抽搐最有效的药物,但近年来核成像使人们对 TS 中的 DA 神经传递有了更深入的了解。基于各种正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)研究的结果,综述的第一部分讨论了 TS 中 DA 功能障碍的四个假设:(i)DA 过度支配,(ii)超敏 DA 受体,(iii)突触前 DA 异常和(iv)DA 紧张-相位功能障碍。根据后一种假设,细胞外空间中紧张型 DA 水平的降低导致轴突末梢中 DA 的浓度更高,并增加了刺激依赖性 DA 的释放。综述的第二部分讨论了 DA 在 TS 的一些主要临床特征中的调节作用,例如与压力或感染的加重以及与感觉运动门控缺陷的关联。