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Large Postural Sways Prevent Foot Tactile Information From Fading: Neurophysiological Evidence.

Authors :
Fabre M
Antoine M
Robitaille MG
Ribot-Ciscar E
Ackerley R
Aimonetti JM
Chavet P
Blouin J
Simoneau M
Mouchnino L
Source :
Cerebral cortex communications [Cereb Cortex Commun] 2020 Dec 28; Vol. 2 (1), pp. tgaa094. Date of Electronic Publication: 2020 Dec 28 (Print Publication: 2021).
Publication Year :
2020

Abstract

Cutaneous foot receptors are important for balance control, and their activation during quiet standing depends on the speed and the amplitude of postural oscillations. We hypothesized that the transmission of cutaneous input to the cortex is reduced during prolonged small postural sways due to receptor adaptation during continued skin compression. Central mechanisms would trigger large sways to reactivate the receptors. We compared the amplitude of positive and negative post-stimulation peaks (P <subscript>50</subscript> N <subscript>90</subscript> ) somatosensory cortical potentials evoked by the electrical stimulation of the foot sole during small and large sways in 16 young adults standing still with their eyes closed. We observed greater P <subscript>50</subscript> N <subscript>90</subscript> amplitudes during large sways compared with small sways consistent with increased cutaneous transmission during large sways. Postural oscillations computed 200 ms before large sways had smaller amplitudes than those before small sways, providing sustained compression within a small foot sole area. Cortical source analyses revealed that during this interval, the activity of the somatosensory areas decreased, whereas the activity of cortical areas engaged in motor planning (supplementary motor area, dorsolateral prefrontal cortex) increased. We concluded that large sways during quiet standing represent self-generated functional behavior aiming at releasing skin compression to reactivate mechanoreceptors. Such balance motor commands create sensory reafference that help control postural sway.<br /> (© The Author(s) 2020. Published by Oxford University Press.)

Details

Language :
English
ISSN :
2632-7376
Volume :
2
Issue :
1
Database :
MEDLINE
Journal :
Cerebral cortex communications
Publication Type :
Academic Journal
Accession number :
34296149
Full Text :
https://doi.org/10.1093/texcom/tgaa094