The Vestibular Drive for Balance Control Is Dependent on Multiple Sensory Cues of Gravity
Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to stand. The strength of this vestibular contribution changes with the presence and quality of sensory cues of balance. Here we investigate whether...
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Published in | Frontiers in physiology Vol. 10; p. 476 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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30.04.2019
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Abstract | Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to stand. The strength of this vestibular contribution changes with the presence and quality of sensory cues of balance. Here we investigate whether the vestibular drive for standing balance also depends on different sensory cues of gravity by examining vestibular-evoked muscle responses when independently varying load and gravity conditions. Standing subjects were braced by a backboard structure that limited whole-body sway to the sagittal plane while load and vestibular cues of gravity were manipulated by: (a) loading the body downward at 1.5 and 2 times body weight (i.e., load cues), and/or (b) exposing subjects to brief periods (20 s) of micro- (<0.05 g) and hyper-gravity (∼1.8 g) during parabolic flights (i.e., vestibular cues). A stochastic electrical vestibular stimulus (0-25 Hz) delivered during these tasks evoked a vestibular-error signal and corrective muscles responses that were used to assess the vestibular drive to standing balance. With additional load, the magnitude of the vestibular-evoked muscle responses progressively increased, however, when these responses were normalized by the ongoing muscle activity, they decreased and plateaued at 1.5 times body weight. This demonstrates that the increased muscle activity necessary to stand with additional load is accompanied a proportionally smaller increase in vestibular input. This reduction in the relative vestibular contribution to balance was also observed when we varied the vestibular cues of gravity, but only during an absence (<0.05 g) and not an excess (∼1.8 g) of gravity when compared to conditions with normal 1 g gravity signals and equivalent load signals. Despite these changes, vestibular-evoked responses were observed in all conditions, indicating that vestibular cues of balance contribute to upright standing even in the near absence of a vestibular signal of gravity (i.e., micro-gravity). Overall, these experiments provide evidence that both load and vestibular cues of gravity influence the vestibular signal processing for the control of standing balance. |
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AbstractList | Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to stand. The strength of this vestibular contribution changes with the presence and quality of sensory cues of balance. Here we investigate whether the vestibular drive for standing balance also depends on different sensory cues of gravity by examining vestibular-evoked muscle responses when independently varying load and gravity conditions. Standing subjects were braced by a backboard structure that limited whole-body sway to the sagittal plane while load and vestibular cues of gravity were manipulated by: (a) loading the body downward at 1.5 and 2 times body weight (i.e., load cues), and/or (b) exposing subjects to brief periods (20 s) of micro- (<0.05 g) and hyper-gravity (∼1.8 g) during parabolic flights (i.e., vestibular cues). A stochastic electrical vestibular stimulus (0–25 Hz) delivered during these tasks evoked a vestibular-error signal and corrective muscles responses that were used to assess the vestibular drive to standing balance. With additional load, the magnitude of the vestibular-evoked muscle responses progressively increased, however, when these responses were normalized by the ongoing muscle activity, they decreased and plateaued at 1.5 times body weight. This demonstrates that the increased muscle activity necessary to stand with additional load is accompanied a proportionally smaller increase in vestibular input. This reduction in the relative vestibular contribution to balance was also observed when we varied the vestibular cues of gravity, but only during an absence (<0.05 g) and not an excess (∼1.8 g) of gravity when compared to conditions with normal 1 g gravity signals and equivalent load signals. Despite these changes, vestibular-evoked responses were observed in all conditions, indicating that vestibular cues of balance contribute to upright standing even in the near absence of a vestibular signal of gravity (i.e., micro-gravity). Overall, these experiments provide evidence that both load and vestibular cues of gravity influence the vestibular signal processing for the control of standing balance. Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to stand. The strength of this vestibular contribution changes with the presence and quality of sensory cues of balance. Here we investigate whether the vestibular drive for standing balance also depends on different sensory cues of gravity by examining vestibular-evoked muscle responses when independently varying load and gravity conditions. Standing subjects were braced by a backboard structure that limited whole-body sway to the sagittal plane while load and vestibular cues of gravity were manipulated by: (a) loading the body downward at 1.5 and 2 times body weight (i.e., load cues), and/or (b) exposing subjects to brief periods (20 s) of micro- (<0.05 g) and hyper-gravity (∼1.8 g) during parabolic flights (i.e., vestibular cues). A stochastic electrical vestibular stimulus (0-25 Hz) delivered during these tasks evoked a vestibular-error signal and corrective muscles responses that were used to assess the vestibular drive to standing balance. With additional load, the magnitude of the vestibular-evoked muscle responses progressively increased, however, when these responses were normalized by the ongoing muscle activity, they decreased and plateaued at 1.5 times body weight. This demonstrates that the increased muscle activity necessary to stand with additional load is accompanied a proportionally smaller increase in vestibular input. This reduction in the relative vestibular contribution to balance was also observed when we varied the vestibular cues of gravity, but only during an absence (<0.05 g) and not an excess (∼1.8 g) of gravity when compared to conditions with normal 1 g gravity signals and equivalent load signals. Despite these changes, vestibular-evoked responses were observed in all conditions, indicating that vestibular cues of balance contribute to upright standing even in the near absence of a vestibular signal of gravity (i.e., micro-gravity). Overall, these experiments provide evidence that both load and vestibular cues of gravity influence the vestibular signal processing for the control of standing balance.Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to stand. The strength of this vestibular contribution changes with the presence and quality of sensory cues of balance. Here we investigate whether the vestibular drive for standing balance also depends on different sensory cues of gravity by examining vestibular-evoked muscle responses when independently varying load and gravity conditions. Standing subjects were braced by a backboard structure that limited whole-body sway to the sagittal plane while load and vestibular cues of gravity were manipulated by: (a) loading the body downward at 1.5 and 2 times body weight (i.e., load cues), and/or (b) exposing subjects to brief periods (20 s) of micro- (<0.05 g) and hyper-gravity (∼1.8 g) during parabolic flights (i.e., vestibular cues). A stochastic electrical vestibular stimulus (0-25 Hz) delivered during these tasks evoked a vestibular-error signal and corrective muscles responses that were used to assess the vestibular drive to standing balance. With additional load, the magnitude of the vestibular-evoked muscle responses progressively increased, however, when these responses were normalized by the ongoing muscle activity, they decreased and plateaued at 1.5 times body weight. This demonstrates that the increased muscle activity necessary to stand with additional load is accompanied a proportionally smaller increase in vestibular input. This reduction in the relative vestibular contribution to balance was also observed when we varied the vestibular cues of gravity, but only during an absence (<0.05 g) and not an excess (∼1.8 g) of gravity when compared to conditions with normal 1 g gravity signals and equivalent load signals. Despite these changes, vestibular-evoked responses were observed in all conditions, indicating that vestibular cues of balance contribute to upright standing even in the near absence of a vestibular signal of gravity (i.e., micro-gravity). Overall, these experiments provide evidence that both load and vestibular cues of gravity influence the vestibular signal processing for the control of standing balance. |
Author | Jonker, Zeb D. van der Putte, Daphne A. M. Hauwert, Christopher M. Arntz, Anne I. Forbes, Patrick A. Frens, Maarten A. |
AuthorAffiliation | 2 Department of Biomechanical Engineering, Faculty of Mechanical, Maritime and Materials Engineering, Delft University of Technology , Delft , Netherlands 1 Department of Neuroscience, Erasmus MC, Erasmus University Medical Center , Rotterdam , Netherlands 3 Department of Rehabilitation Medicine, Erasmus MC, Erasmus University Medical Center , Rotterdam , Netherlands 4 Rijndam Rehabilitation Centre , Rotterdam , Netherlands |
AuthorAffiliation_xml | – name: 4 Rijndam Rehabilitation Centre , Rotterdam , Netherlands – name: 3 Department of Rehabilitation Medicine, Erasmus MC, Erasmus University Medical Center , Rotterdam , Netherlands – name: 2 Department of Biomechanical Engineering, Faculty of Mechanical, Maritime and Materials Engineering, Delft University of Technology , Delft , Netherlands – name: 1 Department of Neuroscience, Erasmus MC, Erasmus University Medical Center , Rotterdam , Netherlands |
Author_xml | – sequence: 1 givenname: Anne I. surname: Arntz fullname: Arntz, Anne I. – sequence: 2 givenname: Daphne A. M. surname: van der Putte fullname: van der Putte, Daphne A. M. – sequence: 3 givenname: Zeb D. surname: Jonker fullname: Jonker, Zeb D. – sequence: 4 givenname: Christopher M. surname: Hauwert fullname: Hauwert, Christopher M. – sequence: 5 givenname: Maarten A. surname: Frens fullname: Frens, Maarten A. – sequence: 6 givenname: Patrick A. surname: Forbes fullname: Forbes, Patrick A. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31114504$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1152/japplphysiol.01398.2006 10.1038/s41467-019-09738-1 10.1113/jphysiol.2007.133264 10.1016/0006-8993(74)90276-5 10.1152/jn.00114.2015 10.1152/japplphysiol.00008.2004 10.1113/jphysiol.2002.019513 10.1159/000046815 10.1007/s00221-004-1982-2 10.1113/jphysiol.2004.079525 10.1152/jn.00343.2014 10.1152/jn.00512.2015 10.1007/s00221-011-2549-7 10.1111/j.1748-1716.1983.tb07212.x 10.3389/fneur.2018.00899 10.1007/BF00237753 10.1016/B978-0-444-63916-5.00004-5 10.1007/s00221-011-2600-8 10.1007/s002210100754 10.1113/jphysiol.2005.092544 10.1016/s0079-6107(96)00009-0 10.1523/JNEUROSCI.0733-14.2014 10.1109/ROBOT.2010.5509378 10.1113/jphysiol.2012.230334 10.1126/science.6729475 10.1113/jphysiol.1994.sp020257 10.1523/jneurosci.1902-16.2016 10.1007/BF00230477 10.1113/jphysiol.2002.029991 10.1016/B978-0-444-63916-5.00003-3 10.1371/journal.pone.0124532 10.1152/jn.00881.2009 10.1016/j.brainresbull.2004.07.008 10.1007/s00221-012-3002-2 10.1109/TNSRE.2011.2140332 10.1088/1741-2560/2/3/S07 10.1007/s004220000196 10.1007/s00221-009-2017-9 10.1016/j.exger.2014.09.020 10.1152/jn.1984.51.6.1236 10.1152/jn.1996.76.6.3994 10.1016/j.gaitpost.2015.10.027 10.1007/BF00237748 |
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Keywords | vestibular-evoked responses gravity electrical vestibular stimulation balance control vestibular system |
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Snippet | Vestibular signals, which encode head movement in space as well as orientation relative to gravity, contribute to the ongoing muscle activity required to... |
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SubjectTerms | balance control electrical vestibular stimulation gravity Physiology vestibular system vestibular-evoked responses |
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Title | The Vestibular Drive for Balance Control Is Dependent on Multiple Sensory Cues of Gravity |
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