|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1Institute of Neurology, Università Cattolica, Rome, Italy; 2Unidad de Neurologia Funcional, Hospital Nacional de Paraplejicos, Finca la Peraleda, Toledo, Spain; 3Neurochirurgia CTO, and 4Neurofisiologia CTO, and 5Fondazione Don C Gnocchi, Rome, Italy; and 6Sobell Department of Neurophysiology, Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, United Kingdom
Submitted 6 April 2006; accepted in final form 22 May 2006
A magnetic transcranial conditioning stimulus given over the motor cortex at intensities below active threshold for obtaining motor-evoked potentials (MEPs) facilitates EMG responses evoked at rest in hand muscles by a suprathreshold magnetic stimulus given 1025 ms later. This is known as intracortical facilitation (ICF). We recorded descending volleys produced by single and paired magnetic motor cortex stimulation through high cervical epidural electrodes implanted for pain relief in six conscious patients. At interstimulus intervals (ISIs) of 10 and 15 ms, although MEP was facilitated, there was no change in the amplitude or number of descending volleys. An additional I wave sometimes was observed at 25 ms ISI. In one subject, we also evaluated the effects of reversing the direction of the induced current in the brain. At 10 ms ISI, the facilitation of the MEPs disappeared and was replaced by slight suppression; at 2 ms ISI, there was a pronounced facilitation of epidural volleys. Subsequent experiments on healthy subjects showed that a conditioning stimulus capable of producing ICF of MEPs had no effect on the EMG response evoked by transmastoidal electrical stimulation of corticospinal tract. We conclude that ICF occurs because either 1) the conditioning stimulus has a (thus far undetected) effect on spinal cord excitability that increases its response to the same amplitude test volley or 2) that it can alter the composition (but not the amplitude) of the descending volleys set up by the test stimulus such that a larger proportion of the activity is destined for the target muscle.
This article has been cited by other articles:
![]() |
O. B.C. Swayne, J. C. Rothwell, N. S. Ward, and R. J. Greenwood Stages of Motor Output Reorganization after Hemispheric Stroke Suggested by Longitudinal Studies of Cortical Physiology Cereb Cortex, August 1, 2008; 18(8): 1909 - 1922. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Vucic, G. A. Nicholson, and M. C. Kiernan Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis Brain, June 1, 2008; 131(6): 1540 - 1550. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Reis, O. B. Swayne, Y. Vandermeeren, M. Camus, M. A. Dimyan, M. Harris-Love, M. A. Perez, P. Ragert, J. C. Rothwell, and L. G. Cohen Contribution of transcranial magnetic stimulation to the understanding of cortical mechanisms involved in motor control J. Physiol., January 15, 2008; 586(2): 325 - 351. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Ni, C. Gunraj, and R. Chen Short interval intracortical inhibition and facilitation during the silent period in human J. Physiol., September 15, 2007; 583(3): 971 - 982. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. D. Roy, J. A. Norton, and M. A. Gorassini Role of Sustained Excitability of the Leg Motor Cortex After Transcranial Magnetic Stimulation in Associative Plasticity J Neurophysiol, August 1, 2007; 98(2): 657 - 667. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Lee, C. Gunraj, and R. Chen The effects of inhibitory and facilitatory intracortical circuits on interhemispheric inhibition in the human motor cortex J. Physiol., May 1, 2007; 580(3): 1021 - 1032. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |