Hawksley Jack, Cavanna Andrea E, Nagai Yoko
North Essex Partnership University NHS Foundation Trust Colchester, UK.
Department of Neuropsychiatry, Birmingham and Solihull Mental Health NHS Trust and School of Clinical and Experimental Medicine, University of Birmingham Birmingham, UK.
Front Neurosci. 2015 May 27;9:117. doi: 10.3389/fnins.2015.00117. eCollection 2015.
Tourette Syndrome (TS) is a neurodevelopmental disorder, consisting of multiple involuntary movements (motor tics) and one or more vocal (phonic) tics. It affects up to one percent of children worldwide, of whom about one third continue to experience symptoms into adulthood. The central neural mechanisms of tic generation are not clearly understood, however recent neuroimaging investigations suggest impaired cortico-striato-thalamo-cortical activity during motor control. In the current manuscript, we will tackle the relatively under-investigated role of the peripheral autonomic nervous system, and its central influences, on tic activity. There is emerging evidence that both sympathetic and parasympathetic nervous activity influences tic expression. Pharmacological treatments which act on sympathetic tone are often helpful: for example, Clonidine (an alpha-2 adrenoreceptor agonist) is often used as first choice medication for treating TS in children due to its good tolerability profile and potential usefulness for co-morbid attention-deficit and hyperactivity disorder. Clonidine suppresses sympathetic activity, reducing the triggering of motor tics. A general elevation of sympathetic tone is reported in patients with TS compared to healthy people, however this observation may reflect transient responses coupled to tic activity. Thus, the presence of autonomic impairments in patients with TS remains unclear. Effect of autonomic afferent input to cortico-striato-thalamo-cortical circuit will be discussed schematically. We additionally review how TS is affected by modulation of central autonomic control through biofeedback and Vagus Nerve Stimulation (VNS). Biofeedback training can enable a patient to gain voluntary control over covert physiological responses by making these responses explicit. Electrodermal biofeedback training to elicit a reduction in sympathetic tone has a demonstrated association with reduced tic frequency. VNS, achieved through an implanted device that gives pulsatile electrical stimulation to the vagus nerve, directly modulates afferent interoceptive signals. The potential efficacy of biofeedback/VNS in TS and the implications for understanding the underlying neural mechanisms of tics will be discussed.
抽动秽语综合征(TS)是一种神经发育障碍,由多种不自主运动(运动性抽动)和一种或多种发声(发声性)抽动组成。它影响着全球多达1%的儿童,其中约三分之一的儿童成年后仍有症状。抽动产生的中枢神经机制尚不清楚,然而最近的神经影像学研究表明,在运动控制过程中皮质-纹状体-丘脑-皮质活动受损。在当前的手稿中,我们将探讨外周自主神经系统及其对抽动活动的中枢影响这一相对研究不足的作用。越来越多的证据表明,交感神经和副交感神经活动都会影响抽动的表达。作用于交感神经张力的药物治疗通常是有帮助的:例如,可乐定(一种α-2肾上腺素能受体激动剂)由于其良好的耐受性和对共病注意力缺陷多动障碍的潜在疗效,常被用作治疗儿童TS的首选药物。可乐定抑制交感神经活动,减少运动性抽动的触发。与健康人相比,TS患者报告有交感神经张力普遍升高的情况,然而这一观察结果可能反映了与抽动活动相关的短暂反应。因此,TS患者自主神经功能障碍的存在仍不明确。将示意性地讨论自主神经传入输入对皮质-纹状体-丘脑-皮质回路的影响。我们还将综述生物反馈和迷走神经刺激(VNS)对中枢自主神经控制的调节如何影响TS。生物反馈训练可以使患者通过使这些反应变得明确来获得对隐蔽生理反应的自主控制。通过电皮生物反馈训练来降低交感神经张力已被证明与抽动频率降低有关。VNS是通过一种植入装置实现的,该装置向迷走神经提供脉冲电刺激,直接调节传入的内感受信号。将讨论生物反馈/VNS在TS中的潜在疗效及其对理解抽动潜在神经机制的意义。