4.6 Article

Brain State-Dependent Transcranial Magnetic Closed-Loop Stimulation Controlled by Sensorimotor Desynchronization Induces Robust Increase of Corticospinal Excitability

Journal

BRAIN STIMULATION
Volume 9, Issue 3, Pages 415-424

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.brs.2016.02.007

Keywords

Event-related desynchronization; Motor cortex plasticity; Sensorimotor rhythm; Beta-band; Brain-computer interface; Brain state-dependent stimulation; Closed-loop stimulation

Funding

  1. Graduate Training Centre of Neuroscience, International Max Planck Research School for Cognitive and Systems Neuroscience, Tuebingen, Germany
  2. German Research Council [DFG] [GH 94/2-1, EC 307]
  3. Federal Ministry of Education and Research [BFNT 01GQ0761, BMBF 16SV3783, BMBF 0316064B, BMBF 16SV5824]

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Background: Desynchronization of sensorimotor rhythmic activity increases instantaneous corticospinal excitability, as indexed by amplitudes of motor-evoked potentials (MEP) elicited by transcranial magnetic stimulation (TMS). The accumulative effect of cortical stimulation in conjunction with sensorimotor desynchronization is, however, unclear. Objective: The aim of this study was to investigate the effects of repetitive pairing event-related desynchronization (ERD) with TMS of the precentral gyrus on corticospinal excitability. Methods: Closed-loop single-pulse TMS was controlled by beta-band (16-22 Hz) ERD during motor-imagery of finger extension and applied within a brain-computer interface environment in eleven healthy subjects. The same number and pattern of stimuli were applied in a control group of eleven subjects during rest, i.e. independent of ERD. To probe for plasticity resistant to depotentiation, stimulation protocols were followed by a depotentiation task. Results: Brain state-dependent application of approximately 300 TMS pulses during beta-ERD resulted in a significant increase of corticospinal excitability. By contrast, the identical stimulation pattern applied independent of beta-ERD in the control experiment resulted in a decrease of corticospinal excitability. These effects persisted beyond the period of stimulation and the depotentiation task. Conclusion: These results could be instrumental in developing new therapeutic approaches such as the application of closed-loop stimulation in the context of neurorehabilitation. (C) 2016 Elsevier Inc. All rights reserved.

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