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Cortical motor neuron excitability during cutaneous silent period.

作者信息

Kaneko K, Kawai S, Taguchi T, Fuchigami Y, Yonemura H, Fujimoto H

机构信息

Department of Orthopedic Surgery, Yamaguchi University Hospital, Ube City, Japan.

出版信息

Electroencephalogr Clin Neurophysiol. 1998 Aug;109(4):364-8. doi: 10.1016/s0924-980x(98)00031-9.

DOI:10.1016/s0924-980x(98)00031-9
PMID:9751300
Abstract

OBJECTIVE

To investigate cortical motor neuron excitability during cutaneous silent period (CSP), motor evoked potentials (MEPs) from abductor pollicis brevis following transcranial magnetic stimulation (TCM) were recorded with and without a conditioning of ipsilateral painful digital nerve electric stimulation.

METHODS

MEPs following TCM were recorded with and without a conditioning stimulation at an interstimulus interval (ISI) from 0 ms to 100ms in 6 controls and four patients who had reduced pain sensation in unilateral upper limbs associated with cervical syringomyelia. In addition MEPs and evoked spinal cord potentials (ESCPs) from cervical epidural space following TCM with and without a conditioning stimulation were recorded in four patients with thoracic myelopathy.

RESULTS

MEP amplitude was clearly attenuated by a conditioning stimulation at an ISI from 40 ms to 80 ms in controls (statistically significant at 60 ms). In patients with cervical syringomyelia, MEP amplitude was attenuated by a conditioning stimulation in asymptomatic hands similarly in controls but that was unchanged by a conditioning stimulation in the symptomatic hand with reduced pain sensation. In patients with thoracic myelopathy MEP amplitude was attenuated by conditioning stimulation similarly in controls, but ESCP amplitude was unchanged.

CONCLUSIONS

We demonstrated that noxious cutaneous nerve stimulation suppressed spinal motor neurons but cortical motor neuron excitability was unchanged during CSP. In clinical practice, measurement of MEP suppression after noxious cutaneous nerve stimulation may provide useful information in patients with damaged pain related nerve fibers.

摘要

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