4.8 Article

TMS-evoked responses are driven by recurrent large-scale network dynamics

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ELIFE
卷 12, 期 -, 页码 -

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eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.83232

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transcranial magnetic stimulation; electroencephalography; computational model; connectome; neural mass model; recurrence; Human

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A compelling approach to understand the complexity of the brain is to analyze the effects of synchronized systematic perturbations both in space and time. In humans, this can be done non-invasively by combining transcranial magnetic stimulation (TMS) and electroencephalography (EEG). The study used source-localized TMS-EEG analyses and whole-brain connectome-based computational modeling to differentiate between local dynamics and network activity in TMS evoked potential (TEP) waveforms. The findings shed light on the importance of recurrent network feedback and inhibitory neural populations in cortical excitability.
A compelling way to disentangle the complexity of the brain is to measure the effects of spatially and temporally synchronized systematic perturbations. In humans, this can be non-invasively achieved by combining transcranial magnetic stimulation (TMS) and electroencephalography (EEG). Spatiotemporally complex and long-lasting TMS-EEG evoked potential (TEP) waveforms are believed to result from recurrent, re-entrant activity that propagates broadly across multiple cortical and subcortical regions, dispersing from and later re-converging on, the primary stimulation site. However, if we loosely understand the TEP of a TMS-stimulated region as the impulse response function of a noisy underdamped harmonic oscillator, then multiple later activity components (waveform peaks) should be expected even for an isolated network node in the complete absence of recurrent inputs. Thus emerges a critically important question for basic and clinical research on human brain dynamics: what parts of the TEP are due to purely local dynamics, what parts are due to reverberant, re-entrant network activity, and how can we distinguish between the two? To disentangle this, we used source-localized TMS-EEG analyses and whole-brain connectome-based computational modelling. Results indicated that recurrent network feedback begins to drive TEP responses from 100 ms post-stimulation, with earlier TEP components being attributable to local reverberatory activity within the stimulated region. Subject-specific estimation of neurophysiological parameters additionally indicated an important role for inhibitory GABAergic neural populations in scaling cortical excitability levels, as reflected in TEP waveform characteristics. The novel discoveries and new software technologies introduced here should be of broad utility in basic and clinical neuroscience research.

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