Title of article :
Transcranial magnetic and electrical stimulation compared: Does TES activate intracortical neuronal circuits?
Author/Authors :
J. Brocke، نويسنده , , K. Irlbacher، نويسنده , , B. Hauptmann، نويسنده , , M. Voss، نويسنده , , S.A. Brandt and A.P. Moulin ، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
9
From page :
2748
To page :
2756
Abstract :
Objective To determine whether, and under which conditions, transcranial electrical stimulation (TES) and transcranial magnetic stimulation (TMS) can activate similar neuronal structures of the human motor cortex, as indicated by electromyographic recordings. Methods Focal TMS was performed on three subjects inducing a postero-anterior directed current (p-a), TES with postero-anteriorly (p-a) and latero-medially (l-m) oriented electrodes. We analyzed the onset latencies and amplitudes (single-pulse) and intracortical inhibition and excitation (paired-pulse). Results TMS p-a and TES p-a produced muscle responses with the same onset latency, while TES l-m led to 1.4–1.9 ms shorter latencies. Paired-pulse TMS p-a and TES p-a induced inhibition at short inter-stimulus intervals (ISI) (maximum: 2–3 ms) and facilitation at longer ISIs (maximum: 10 ms). No inhibition but a strong facilitation was obtained from paired-pulse TES l-m (ISIs 1–5 ms). Conclusions Our findings support the hypothesis, that current direction is the most relevant factor in determining the mode of activation for both TMS and TES: TMS p-a and TES p-a are likely to activate the corticospinal neurons indirectly. In contrast, TES l-m may preferentially activate the corticospinal fibres directly, distant of the neuronal body. Significance TES is a suitable tool to induce intracortical inhibition and excitation.
Keywords :
Human motor cortex , Transcranial magnetic stimulation , Intracortical facilitation , Transcranial electrical stimulation , Intracortical inhibition
Journal title :
Clinical Neurophysiology
Serial Year :
2005
Journal title :
Clinical Neurophysiology
Record number :
523459
Link To Document :
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