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揭示深部脑刺激的作用机制:激活、抑制,还是两者兼有。

Uncovering the mechanism(s) of action of deep brain stimulation: activation, inhibition, or both.

作者信息

McIntyre Cameron C, Savasta Marc, Kerkerian-Le Goff Lydia, Vitek Jerrold L

机构信息

Department of Neurology, Emory University School of Medicine, Woodruff Memorial Research Building, Suite 6000, 1639 Pierce Drive, Atlanta, GA 30322, USA.

出版信息

Clin Neurophysiol. 2004 Jun;115(6):1239-48. doi: 10.1016/j.clinph.2003.12.024.

Abstract

High-frequency deep brain stimulation (DBS) of the thalamus or basal ganglia represents an effective clinical technique for the treatment of several medically refractory movement disorders. However, understanding of the mechanisms responsible for the therapeutic action of DBS remains elusive. The goal of this review is to address our present knowledge of the effects of high-frequency stimulation within the central nervous system and comment on the functional implications of this knowledge for uncovering the mechanism(s) of DBS. Four general hypotheses have been developed to explain the mechanism(s) of DBS: depolarization blockade, synaptic inhibition, synaptic depression, and stimulation-induced modulation of pathological network activity. Using the results from functional imaging, neurochemistry, neural recording, and neural modeling experiments we address the general hypotheses and attempt to reconcile what have been considered conflicting results from these different research modalities. Our analysis suggests stimulation-induced modulation of pathological network activity represents the most likely mechanism of DBS; however, several open questions remain to explicitly link the effects of DBS with therapeutic outcomes.

摘要

对丘脑或基底神经节进行高频深部脑刺激(DBS)是治疗几种药物难治性运动障碍的一种有效临床技术。然而,对于DBS治疗作用的机制仍不清楚。本综述的目的是阐述我们目前对中枢神经系统内高频刺激作用的了解,并评论这些知识对于揭示DBS机制的功能意义。已经提出了四种一般假设来解释DBS的机制:去极化阻滞、突触抑制、突触抑制和刺激诱导的病理性网络活动调节。利用功能成像、神经化学、神经记录和神经建模实验的结果,我们探讨了这些一般假设,并试图调和这些不同研究方式中被认为相互矛盾的结果。我们的分析表明,刺激诱导的病理性网络活动调节是DBS最可能的机制;然而,仍有几个悬而未决的问题需要明确将DBS的作用与治疗结果联系起来。

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