Although cathodal transcranial d.c. stimulation (tDCS) decreases cortical excitability, the mechanisms underlying DC-induced changes remain largely unclear. In this study we investigated the effect of cathodal DC stimulation on spontaneous neural activity and on motor responses evoked by stimulation of the central and peripheral nervous system. We studied 17 healthy volunteers. Transcranial magnetic stimulation (TMS) and transcranial elec. stimulation (TES) of the motor area were used to study the effects of cathodal tDCS (1.5 mA, 10 min) on resting motor threshold and motor evoked potentials (MEPs) recorded from the contralateral first dorsal interosseous muscle (FDI). The electroencephalog. (EEG) activity in response to cathodal tDCS was analyzed by power spectral d. (PSD). Motor axonal excitability changes in response to transcutaneous DC stimulation of the ulnar nerve (0.3 mA, 10 min) were assessed by testing changes in the size of the compd. muscle action potential (CMAP) elicited by submaximal nerve stimulation. Cathodal tDCS over the motor area for 10 min increased the motor threshold and decreased the size of MEPs evoked by TMS for at least 60 min after current offset (t0 71.7 ? 5%, t20 50.8 ? 11%, t40 47.7 ? 7.7%, and t60 39.7 ? 6.4%, P < 0.01). The tDCS also significantly decreased the size of MEPs elicited by TES (t0 64 ? 16.4%, P = 0.09; t20 67.6 ? 10.8%, P = 0.06; and t40 58.3 ? 9.9%, P < 0.05). At the same time in the EEG the power of delta (2-4 Hz) and theta (4-7 Hz) rhythms increased (delta 181.1 ? 40.2, P < 0.05; and theta 138.7 ? 27.6, P = 0.07). At the peripheral level cathodal DC stimulation increased the size of the ulnar nerve CMAP (175 ? 34.3%, P < 0.05). Our findings demonstrate that the after-effects of tDCS have a non-synaptic mechanism of action based upon changes in neural membrane function.

Non-synaptic mechanisms underlie the after-effects of cathodal transcutaneous direct current stimulation of the human brain / G. Ardolino, B. Bossi, S. Barbieri, A Priori. - In: THE JOURNAL OF PHYSIOLOGY. - ISSN 0022-3751. - 568:Pt 2(2005 Oct 15), pp. 653-663.

Non-synaptic mechanisms underlie the after-effects of cathodal transcutaneous direct current stimulation of the human brain

A Priori
2005

Abstract

Although cathodal transcranial d.c. stimulation (tDCS) decreases cortical excitability, the mechanisms underlying DC-induced changes remain largely unclear. In this study we investigated the effect of cathodal DC stimulation on spontaneous neural activity and on motor responses evoked by stimulation of the central and peripheral nervous system. We studied 17 healthy volunteers. Transcranial magnetic stimulation (TMS) and transcranial elec. stimulation (TES) of the motor area were used to study the effects of cathodal tDCS (1.5 mA, 10 min) on resting motor threshold and motor evoked potentials (MEPs) recorded from the contralateral first dorsal interosseous muscle (FDI). The electroencephalog. (EEG) activity in response to cathodal tDCS was analyzed by power spectral d. (PSD). Motor axonal excitability changes in response to transcutaneous DC stimulation of the ulnar nerve (0.3 mA, 10 min) were assessed by testing changes in the size of the compd. muscle action potential (CMAP) elicited by submaximal nerve stimulation. Cathodal tDCS over the motor area for 10 min increased the motor threshold and decreased the size of MEPs evoked by TMS for at least 60 min after current offset (t0 71.7 ? 5%, t20 50.8 ? 11%, t40 47.7 ? 7.7%, and t60 39.7 ? 6.4%, P < 0.01). The tDCS also significantly decreased the size of MEPs elicited by TES (t0 64 ? 16.4%, P = 0.09; t20 67.6 ? 10.8%, P = 0.06; and t40 58.3 ? 9.9%, P < 0.05). At the same time in the EEG the power of delta (2-4 Hz) and theta (4-7 Hz) rhythms increased (delta 181.1 ? 40.2, P < 0.05; and theta 138.7 ? 27.6, P = 0.07). At the peripheral level cathodal DC stimulation increased the size of the ulnar nerve CMAP (175 ? 34.3%, P < 0.05). Our findings demonstrate that the after-effects of tDCS have a non-synaptic mechanism of action based upon changes in neural membrane function.
Settore MED/26 - Neurologia
15-ott-2005
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/14587
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