Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA; Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52245, USA; Cognitive Control Collaborative, University of Iowa, Iowa City, IA 52245, USA; Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242, USA.
Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52245, USA; Cognitive Control Collaborative, University of Iowa, Iowa City, IA 52245, USA.
Curr Biol. 2022 Sep 12;32(17):3785-3791.e3. doi: 10.1016/j.cub.2022.06.067. Epub 2022 Jul 15.
Common cortico-basal ganglia models of motor control suggest a key role for the subthalamic nucleus (STN) in motor inhibition. In particular, when already-initiated actions have to be suddenly stopped, the STN is purportedly recruited via a hyperdirect pathway to net inhibit the cortico-motor system in a broad, non-selective fashion. Indeed, the suppression of cortico-spinal excitability (CSE) during rapid action stopping extends beyond the stopped muscle and affects even task-irrelevant motor representations. Although such non-selective CSE suppression has long been attributed to the broad inhibitory influence of STN on the motor system, causal evidence for this association is hitherto lacking. Here, 20 Parkinson's disease patients treated with STN deep-brain stimulation (DBS) and 20 matched healthy controls performed a verbal stop-signal task while CSE was measured from a task-unrelated hand muscle. DBS allowed a causal manipulation of STN, while CSE was measured using transcranial magnetic stimulation (TMS) over primary motor cortex and concurrent electromyography. In patients OFF-DBS and controls, the CSE of the hand was non-selectively suppressed when the verbal response was successfully stopped. Crucially, this effect disappeared when STN was disrupted via DBS in the patient group. Using this unique combination of DBS and TMS during human behavior, the current study provides first causal evidence that STN is likely involved in non-selectively suppressing the physiological excitability of the cortico-motor system during action stopping. This confirms a core prediction of long-held cortico-basal ganglia circuit models of movement. The absence of cortico-motor inhibition during STN-DBS may also provide potential insights into the common side effects of STN-DBS, such as increased impulsivity..
常见的皮质基底节运动控制模型表明,丘脑底核(STN)在运动抑制中起着关键作用。特别是,当已经开始的动作必须突然停止时,据称 STN 通过一个超直接途径被招募,以广泛、非选择性的方式抑制皮质-运动系统。事实上,在快速动作停止期间皮质脊髓兴奋性(CSE)的抑制不仅延伸到停止的肌肉,而且还影响到与任务无关的运动表现。尽管这种非选择性的 CSE 抑制长期以来归因于 STN 对运动系统的广泛抑制影响,但迄今为止缺乏这种关联的因果证据。在这里,20 名接受 STN 深部脑刺激(DBS)治疗的帕金森病患者和 20 名匹配的健康对照者在执行言语停止信号任务时,同时从一个与任务无关的手部肌肉测量 CSE。DBS 允许对 STN 进行因果操作,而 CSE 则使用经颅磁刺激(TMS)在初级运动皮层上进行测量,并同时进行肌电图。在患者 OFF-DBS 和对照组中,当言语反应成功停止时,手部的 CSE 被非选择性地抑制。至关重要的是,当通过 DBS 在患者组中破坏 STN 时,这种效应消失了。通过在人类行为中使用这种独特的 DBS 和 TMS 组合,本研究首次提供了因果证据,表明 STN 可能参与了在动作停止期间非选择性地抑制皮质-运动系统的生理兴奋性。这证实了长期持有的皮质基底节运动回路模型的核心预测。在 STN-DBS 期间皮质运动抑制的缺失也可能为 STN-DBS 的常见副作用提供潜在的见解,例如冲动性增加。