Cross-Modal Calibration of Vestibular Afference for Human Balance.

To determine how the vestibular sense controls balance, we used instantaneous head angular velocity to drive a galvanic vestibular stimulus so that afference would signal that head movement was faster or slower than actual. In effect, this changed vestibular afferent gain. This increased sway 4-fold...

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Main Authors: Martin E Héroux, Tammy C Y Law, Richard C Fitzpatrick, Jean-Sébastien Blouin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4403994?pdf=render
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spelling doaj-9d798e02c7df42858688d877673990d32020-11-25T01:52:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012453210.1371/journal.pone.0124532Cross-Modal Calibration of Vestibular Afference for Human Balance.Martin E HérouxTammy C Y LawRichard C FitzpatrickJean-Sébastien BlouinTo determine how the vestibular sense controls balance, we used instantaneous head angular velocity to drive a galvanic vestibular stimulus so that afference would signal that head movement was faster or slower than actual. In effect, this changed vestibular afferent gain. This increased sway 4-fold when subjects (N = 8) stood without vision. However, after a 240 s conditioning period with stable balance achieved through reliable visual or somatosensory cues, sway returned to normal. An equivalent galvanic stimulus unrelated to sway (not driven by head motion) was equally destabilising but in this situation the conditioning period of stable balance did not reduce sway. Reflex muscle responses evoked by an independent, higher bandwidth vestibular stimulus were initially reduced in amplitude by the galvanic stimulus but returned to normal levels after the conditioning period, contrary to predictions that they would decrease after adaptation to increased sensory gain and increase after adaptation to decreased sensory gain. We conclude that an erroneous vestibular signal of head motion during standing has profound effects on balance control. If it is unrelated to current head motion, the CNS has no immediate mechanism of ignoring the vestibular signal to reduce its influence on destabilising balance. This result is inconsistent with sensory reweighting based on disturbances. The increase in sway with increased sensory gain is also inconsistent with a simple feedback model of vestibular reflex action. Thus, we propose that recalibration of a forward sensory model best explains the reinterpretation of an altered reafferent signal of head motion during stable balance.http://europepmc.org/articles/PMC4403994?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Martin E Héroux
Tammy C Y Law
Richard C Fitzpatrick
Jean-Sébastien Blouin
spellingShingle Martin E Héroux
Tammy C Y Law
Richard C Fitzpatrick
Jean-Sébastien Blouin
Cross-Modal Calibration of Vestibular Afference for Human Balance.
PLoS ONE
author_facet Martin E Héroux
Tammy C Y Law
Richard C Fitzpatrick
Jean-Sébastien Blouin
author_sort Martin E Héroux
title Cross-Modal Calibration of Vestibular Afference for Human Balance.
title_short Cross-Modal Calibration of Vestibular Afference for Human Balance.
title_full Cross-Modal Calibration of Vestibular Afference for Human Balance.
title_fullStr Cross-Modal Calibration of Vestibular Afference for Human Balance.
title_full_unstemmed Cross-Modal Calibration of Vestibular Afference for Human Balance.
title_sort cross-modal calibration of vestibular afference for human balance.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description To determine how the vestibular sense controls balance, we used instantaneous head angular velocity to drive a galvanic vestibular stimulus so that afference would signal that head movement was faster or slower than actual. In effect, this changed vestibular afferent gain. This increased sway 4-fold when subjects (N = 8) stood without vision. However, after a 240 s conditioning period with stable balance achieved through reliable visual or somatosensory cues, sway returned to normal. An equivalent galvanic stimulus unrelated to sway (not driven by head motion) was equally destabilising but in this situation the conditioning period of stable balance did not reduce sway. Reflex muscle responses evoked by an independent, higher bandwidth vestibular stimulus were initially reduced in amplitude by the galvanic stimulus but returned to normal levels after the conditioning period, contrary to predictions that they would decrease after adaptation to increased sensory gain and increase after adaptation to decreased sensory gain. We conclude that an erroneous vestibular signal of head motion during standing has profound effects on balance control. If it is unrelated to current head motion, the CNS has no immediate mechanism of ignoring the vestibular signal to reduce its influence on destabilising balance. This result is inconsistent with sensory reweighting based on disturbances. The increase in sway with increased sensory gain is also inconsistent with a simple feedback model of vestibular reflex action. Thus, we propose that recalibration of a forward sensory model best explains the reinterpretation of an altered reafferent signal of head motion during stable balance.
url http://europepmc.org/articles/PMC4403994?pdf=render
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