Birdno Merrill J, Tang Wei, Dostrovsky Jonathan O, Hutchison William D, Grill Warren M
Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.
Department of Physiology, University of Toronto, Toronto, Ontario, Canada.
PLoS One. 2014 May 7;9(5):e96026. doi: 10.1371/journal.pone.0096026. eCollection 2014.
Thalamic deep brain stimulation (DBS) is an effective treatment for tremor, but the mechanisms of action remain unclear. Previous studies of human thalamic neurons to noted transient rebound bursting activity followed by prolonged inhibition after cessation of high frequency extracellular stimulation, and the present study sought to identify the mechanisms underlying this response. Recordings from 13 thalamic neurons exhibiting low threshold spike (LTS) bursting to brief periods of extracellular stimulation were made during surgeries to implant DBS leads in 6 subjects with Parkinson's disease. The response immediately after cessation of stimulation included a short epoch of burst activity, followed by a prolonged period of silence before a return to LTS bursting. A computational model of a population of thalamocortical relay neurons and presynaptic axons terminating on the neurons was used to identify cellular mechanisms of the observed responses. The model included the actions of neuromodulators through inhibition of a non-pertussis toxin sensitive K(+) current (I(KL)), activation of a pertussis toxin sensitive K(+) current (I(KG)), and a shift in the activation curve of the hyperpolarization-activated cation current (I(h)). The model replicated well the measured responses, and the prolonged inhibition was associated most strongly with changes in I(KG) while modulation of I(KL) or I(h) had minimal effects on post-stimulus inhibition suggesting that neuromodulators released in response to high frequency stimulation are responsible for mediating the post-stimulation bursting and subsequent long duration silence of thalamic neurons. The modeling also indicated that the axons of the model neurons responded robustly to suprathreshold stimulation despite the inhibitory effects on the soma. The findings suggest that during DBS the axons of thalamocortical neurons are activated while the cell bodies are inhibited thus blocking the transmission of pathological signals through the network and replacing them with high frequency regular firing.
丘脑深部脑刺激(DBS)是治疗震颤的一种有效方法,但其作用机制仍不清楚。先前对人类丘脑神经元的研究指出,在高频细胞外刺激停止后会出现短暂的反弹爆发活动,随后是长时间的抑制,本研究旨在确定这种反应背后的机制。在为6名帕金森病患者植入DBS电极的手术过程中,对13个丘脑神经元进行了记录,这些神经元对短暂的细胞外刺激表现出低阈值尖峰(LTS)爆发。刺激停止后的立即反应包括一段短暂的爆发活动期,随后是一段长时间的沉默,之后才恢复LTS爆发。使用一个丘脑皮质中继神经元群体和终止于这些神经元的突触前轴突的计算模型来确定所观察到的反应的细胞机制。该模型包括神经调质通过抑制一种对百日咳毒素不敏感的钾电流(I(KL))、激活一种对百日咳毒素敏感的钾电流(I(KG))以及超极化激活阳离子电流(I(h))的激活曲线的移位所产生的作用。该模型很好地复制了测量到的反应,长时间的抑制与I(KG)的变化最密切相关,而I(KL)或I(h)的调节对刺激后抑制的影响最小,这表明对高频刺激做出反应而释放的神经调质负责介导丘脑神经元刺激后的爆发和随后的长时间沉默。建模还表明,尽管对胞体有抑制作用,但模型神经元的轴突对阈上刺激有强烈反应。这些发现表明,在DBS期间,丘脑皮质神经元的轴突被激活,而细胞体被抑制,从而阻断病理信号通过网络的传递,并用高频规则放电取而代之。