Brain, Vol. 126, No. 4, 988-1000,
April 2003
© 2003 Guarantors of Brain
doi: 10.1093/brain/awg088
Changes in propriospinally mediated excitation of upper limb motoneurons in stroke patients
INSERM EMI E03 49, Neurophysiologie Clinique, Rééducation, Hôpital de la Salpêtrière, Paris, France
Correspondence to: Professor Emmanuel Pierrot-Deseilligny, Neurophysiologie Clinique, Rééducation, Hôpital de la Salpêtrière, 47 boulevard de lHôpital, 75651 Paris cedex 13, France E-mail: emmanuel.pierrot-deseilligny{at}chups.jussieu.fr
It has been argued that, in humans, a part of the descending command to upper limb motoneurons is transmitted through cervical propriospinal premotoneurons. We explored whether excitation of these putative propriospinal neurons projecting onto extensor carpi radialis (ECR) motoneurons was modified in patients recovering from stroke. Suppression of the voluntary on-going ECR EMG activity by stimulation of cutaneous afferents in the superficial radial nerve was used to estimate the component of the descending command passing through the propriospinal relay. The degree of suppression was assessed on both sides of 30 stroke patients (divided into two groups, whether recovery of wrist extension was poor or good by the time of the investigation) and of 34 age-matched controls. Single cutaneous volleys elicited a suppression which was symmetrical and of the same degree in patients and controls. In contrast, the amount of on-going EMG suppression produced by a train, which was symmetrical in normal subjects, was asymmetrical in most stroke patients: it indeed was significantly greater on the affected side of stroke patients with poor recovery of wrist extension than (i) in their non-affected side; (ii) in controls; and (iii) in the affected side of patients with good recovery. Cutaneous suppression of the H reflex, the motor evoked potential (MEP) and the on-going EMG was compared in three patients with poor recovery by the time of the first test; there was a small suppression of the H reflex on the affected side, but the asymmetry was much less than that of the on-going EMG and the MEP. In patients explored twice during the course of recovery, the asymmetry in the suppression of the on-going EMG tended to disappear, while recovery of wrist extension improved. This suggests that, when patients have not yet recovered, a relatively greater component of the descending command is mediated through the propriospinal relay. The findings are consistent with transiently increased efficacy of descending (possibly reticulospinal) projections onto propriospinal neurons, due to hyperexcitability of these neurons or unmasking and/or reorganization of the projections to them.
![]()
CiteULike
Connotea
Del.icio.us What's this?
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] |
||||
![]() |
M. D. Lewek, T. G. Hornby, Y. Y. Dhaher, and B. D. Schmit Prolonged Quadriceps Activity Following Imposed Hip Extension: A Neurophysiological Mechanism for Stiff-Knee Gait? J Neurophysiol, December 1, 2007; 98(6): 3153 - 3162. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Iglesias, V. Marchand-Pauvert, G. Lourenco, D. Burke, and E. Pierrot-Deseilligny Task-related changes in propriospinal excitation from hand muscles to human flexor carpi radialis motoneurones J. Physiol., August 1, 2007; 582(3): 1361 - 1379. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. G. Martin, S. C. Gandevia, and J. L. Taylor Muscle fatigue changes cutaneous suppression of propriospinal drive to human upper limb muscles J. Physiol., April 1, 2007; 580(1): 211 - 223. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. H. Dobkin Behavioral, Temporal, and Spatial Targets for Cellular Transplants as Adjuncts to Rehabilitation for Stroke Stroke, February 1, 2007; 38(2): 832 - 839. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. L. Kline, B. D. Schmit, and D. G. Kamper Exaggerated interlimb neural coupling following stroke Brain, January 1, 2007; 130(1): 159 - 169. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. I.E. Renner, H. Woldag, and H. Hummelsheim Central Compensation at Short Muscle Range Is Differentially Affected in Cortical Versus Subcortical Strokes Stroke, August 1, 2006; 37(8): 2076 - 2080. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. S. Ward, J. M. Newton, O. B. C. Swayne, L. Lee, A. J. Thompson, R. J. Greenwood, J. C. Rothwell, and R. S. J. Frackowiak Motor system activation after subcortical stroke depends on corticospinal system integrity Brain, March 1, 2006; 129(3): 809 - 819. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Jankowska and S. A. Edgley How Can Corticospinal Tract Neurons Contribute to Ipsilateral Movements? A Question With Implications for Recovery of Motor Functions Neuroscientist, February 1, 2006; 12(1): 67 - 79. [Abstract] [PDF] |
||||
![]() |
S. Sasaki, T. Isa, L.-G. Pettersson, B. Alstermark, K. Naito, K. Yoshimura, K. Seki, and Y. Ohki Dexterous Finger Movements in Primate Without Monosynaptic Corticomotoneuronal Excitation J Neurophysiol, November 1, 2004; 92(5): 3142 - 3147. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. H. Dobkin Editorial Comment--Functional MRI: A Potential Physiologic Indicator for Stroke Rehabilitation Interventions Stroke, May 1, 2003; 34 (5): e26 - e28. [Full Text] |
||||





