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图雷特综合征中的胆碱能机制。

Cholinergic mechanisms in Gilles de la Tourette's syndrome.

作者信息

Sandyk R

机构信息

NeuroCommunication Research Laboratories, Danbury, CT 06811, USA.

出版信息

Int J Neurosci. 1995 Mar;81(1-2):95-100. doi: 10.3109/00207459509015301.

DOI:10.3109/00207459509015301
PMID:7775075
Abstract

Gilles de la Tourette syndrome (GTS), a chronic, familial, neuropsychiatric disorder of unknown etiology, is characterized clinically by the presence of motor and vocal tics that wax and wane in severity over time and by the occurrence of a variety of neurobehavioral disturbances including hyperactivity, self-mutilatory behavior, obsessive compulsive behavior, learning disabilities, and conduct disorder. Pharmacological studies suggest that the tics of GTS result from dysfunction of monoaminergic systems, more specifically from increased dopaminergic activity due to postsynaptic dopamine receptor supersensitivity. However, given that striatal dopaminergic and cholinergic systems exhibit reciprocal antagonism in other movement disorders such as Parkinsonism and chorea, it is conceivable that the cholinergic system is implicated in the disease. In the present communication it is proposed that: (a) the emergence of motor and vocal tics in GTS is associated with increased central cholinergic activity; (b) cholinergic overactivity is involved in the manifestation of other symptoms in GTS including depression, sleep disorders, motion sickness, pain, sensory tics, and the waxing and waning course of the disease; (c) abnormalities of the cholinergic system support previous evidence linking GTS with delayed cerebral maturation in a subset of young patients; and (d) drugs which stimulate cholinergic receptors may exacerbate symptoms of GTS, and as with dopamine agonists, should be avoided in patients with GTS.

摘要

Gilles de la Tourette综合征(GTS)是一种病因不明的慢性、家族性神经精神疾病,其临床特征为运动性和发声性抽动,其严重程度随时间波动,还伴有多种神经行为障碍,包括多动、自残行为、强迫行为、学习障碍和品行障碍。药理学研究表明,GTS的抽动是由单胺能系统功能障碍引起的,更具体地说是由于突触后多巴胺受体超敏导致多巴胺能活性增加。然而,鉴于纹状体多巴胺能和胆碱能系统在帕金森病和舞蹈病等其他运动障碍中表现出相互拮抗作用,可以推测胆碱能系统与该疾病有关。在本通讯中,我们提出:(a)GTS中运动性和发声性抽动的出现与中枢胆碱能活性增加有关;(b)胆碱能活动过度参与了GTS中其他症状的表现,包括抑郁、睡眠障碍、晕动病、疼痛、感觉性抽动以及疾病的波动病程;(c)胆碱能系统的异常支持了先前将GTS与一部分年轻患者大脑发育延迟联系起来的证据;(d)刺激胆碱能受体的药物可能会加重GTS的症状,与多巴胺激动剂一样,GTS患者应避免使用。

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