Moll G H, Heinrich H, Rothenberger A
Klinik und Poliklinik für Kinder- und Jugendpsychiatrie und Psychotherapie, Georg-August-Universität Göttingen.
Z Kinder Jugendpsychiatr Psychother. 2001 Nov;29(4):312-23. doi: 10.1024//1422-4917.29.4.312.
Motor system excitability can be investigated in vivo by means of single and paired pulse transcranial magnetic stimulation (TMS). Whereas the cortical silent period reflects the general degree of inhibitory mechanisms mainly within the sensorimotor loop, intracortical excitability measures the focused degree of inhibitory and facilitatory mechanisms within the motor cortex. In child and adolescent psychiatric disorders with uncontrollable motor behavior such as tics in tic disorder or motoric hyperactivity in attention deficit hyperactivity disorder (ADHD), different dysfunctional patterns of motor system excitability could be demonstrated compared to age-matched healthy controls: (1) In tic disorder, a shortened cortical silent period was observed, providing evidence of deficient inhibitory mechanisms within the sensorimotor loop, probably primarily at the level of the basal ganglia. (2) In ADHD, a decreased intracortical inhibition was found, probably reflecting deficient inhibitory mechanisms within the motor cortex (but enhancement of intracortical inhibition after oral intake of 10 mg methylphenidate). In order to investigate neurophysiological aspects of comorbidity, (3) motor system excitability was also measured in children with combined ADHD and tic disorder. The findings of a reduced intracortical inhibition as well as a shortened cortical silent period in these comorbid children provide evidence of additive effects at the level of motor system excitability. These decreased inhibitory mechanisms within the entire sensorimotor loop and especially the motor cortex could be essential neurobiological substrates of the deficient inhibitory motor control and regulation, respectively, in tic disorder and ADHD.
运动系统兴奋性可通过单脉冲和双脉冲经颅磁刺激(TMS)在体内进行研究。皮质静息期反映了主要在感觉运动环路内抑制机制的总体程度,而皮质内兴奋性则测量运动皮质内抑制和易化机制的集中程度。在患有无法控制的运动行为的儿童和青少年精神疾病中,如抽动障碍中的抽动或注意力缺陷多动障碍(ADHD)中的运动性多动,与年龄匹配的健康对照相比,可以证明运动系统兴奋性存在不同的功能失调模式:(1)在抽动障碍中,观察到皮质静息期缩短,这证明感觉运动环路内存在抑制机制缺陷,可能主要在基底神经节水平。(2)在ADHD中,发现皮质内抑制降低,这可能反映了运动皮质内抑制机制的缺陷(但口服10mg哌甲酯后皮质内抑制增强)。为了研究共病的神经生理学方面,(3)还对患有ADHD和抽动障碍合并症的儿童进行了运动系统兴奋性测量。这些共病儿童皮质内抑制降低以及皮质静息期缩短的结果证明了在运动系统兴奋性水平上的叠加效应。整个感觉运动环路尤其是运动皮质内这些降低的抑制机制可能分别是抽动障碍和ADHD中抑制性运动控制和调节缺陷的重要神经生物学基础。