A Model of TMS-induced I-waves in Motor Cortex

被引:97
作者
Rusu, Catalin V. [1 ,4 ,6 ]
Murakami, Max [1 ,5 ]
Ziemann, Ulf [2 ,3 ]
Triesch, Jochen [1 ,5 ]
机构
[1] Frankfurt Inst Adv Studies, D-60438 Frankfurt, Germany
[2] Univ Tubingen, Dept Neurol & Stroke, Tubingen, Germany
[3] Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany
[4] Romanian Inst Sci & Technol, Ctr Cognit & Neural Studies Coneural, Cluj Napoca, Romania
[5] Goethe Univ Frankfurt, Dept Phys, D-60054 Frankfurt, Germany
[6] Univ Babes Bolyai, Dept Comp Sci, R-3400 Cluj Napoca, Romania
关键词
Transcranial stimulation; Motor cortex; I-waves; Computational model; Neuron; TRANSCRANIAL MAGNETIC STIMULATION; CORTICAL EXCITABILITY; VOLUNTARY CONTRACTION; PYRAMIDAL TRACT; METABOLIC COST; LAYER; 2/3; INHIBITION; NEURONS; FACILITATION; ACTIVATION;
D O I
10.1016/j.brs.2014.02.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Transcranial magnetic stimulation (TMS) allows to manipulate neural activity non-invasively, and much research is trying to exploit this ability in clinical and basic research settings. In a standard TMS paradigm, single-pulse stimulation over motor cortex produces repetitive responses in descending motor pathways called I-waves. However, the details of how TMS induces neural activity patterns in cortical circuits to produce these responses remain poorly understood. According to a traditional view, I-waves are due to repetitive synaptic inputs to pyramidal neurons in layer 5 (L5) of motor cortex, but the potential origin of such repetitive inputs is unclear. Objective/hypothesis: Here we aim to test the plausibility of an alternative mechanism behind D-and I-wave generation through computational modeling. This mechanism relies on the broad distribution of conduction delays of synaptic inputs arriving at different parts of L5 cells' dendritic trees and their spike generation mechanism. Methods: Our model consists of a detailed L5 pyramidal cell and a population of layer 2 and 3 (L2/3) neurons projecting onto it with synapses exhibiting short-term depression. I-waves are simulated as superpositions of spike trains from a large population of L5 cells. Results: Our model successfully reproduces all basic characteristics of I-waves observed in epidural responses during in vivo recordings of conscious humans. In addition, it shows how the complex morphology of L5 neurons might play an important role in the generation of I-waves. In the model, later I-waves are formed due to inputs to distal synapses, while earlier ones are driven by synapses closer to the soma. Finally, the model offers an explanation for the inhibition and facilitation effects in paired-pulse stimulation protocols. Conclusions: In contrast to previous models, which required either neural oscillators or chains of inhibitory interneurons acting upon L5 cells, our model is fully feed-forward without lateral connections or loops. It parsimoniously explains findings from a range of experiments and should be considered as a viable alternative explanation of the generating mechanism of I-waves. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:401 / 414
页数:14
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