Brain, Vol. 116, No. 3, 511-525, 1993
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research-article |
Rapid modulation of human cortical motor outputs following ischaemic nerve block
1Human Cortical Physiology Unit, Human Motor Control Section, Medical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda New York, USA 2Departments of Physiology and Neurology, State University of New York Science Center, Brooklyn New York, USA
Correspondence to:
Correspondence to: Leonardo G. Cohen, MD, Bldg 10, Room 5N226, NINDS, NIH, Bethesda, MD 20892, USA.
The amplitudes of motor evoked potentials to transcranial magnetic stimulation from muscles immediately proximal to a temporarily anaesthetized [Bier's block] human forearm increase in minutes after the onset of anaesthesia and return to control values after the anaesthesia subsides. In order to determine the level at which the early modulation of human motor outputs takes place, we recorded maximal H reflexes, peripheral M responses, motor evoked potentials to transcranial magnetic stimulation, and motor evoked potentials to transcranial electrical stimulation and spinal electrical stimulation from a muscle immediately proximal to a limb segment made ischaemic by a pneumatic tourniquest. The amplitudes of motor evoked potentials to transcranial magnetic stimulation, but not to transcranial electrical stimulation and spinal electrical stimulation, were larger during ischaemia, implying that the site of change was in the motor cortex. The maximal H/M ratios were unaffected by ischaemia, indicating that
-motor neuron excitability to segmental la inputs remained unchanged. The map of cortical representation areas for this muscle obtained with transcranial magnetic stimulation was also enlarged. Taken together, our findings suggest that the temporary removal by ischaemic nerve block of myelinated afferent inputs reduces inhibition at the motor cortical level and that this disinhibition is responsible for the increased excitability of the cortico-spinal system.
Received June 3, 1992. Revised October 15, 1992. Accepted November 25, 1992.
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