scispace - formally typeset
Search or ask a question
Journal ArticleDOI

Disentangling the visual, motor and representational effects of vestibular input.

TL;DR: It is suggested that vestibular information contributes to computation of egocentric representations by affecting the internal representation of the body midline.
About: This article is published in Cortex.The article was published on 2018-07-01 and is currently open access. It has received 10 citations till now. The article focuses on the topics: Vestibular system.

Summary (3 min read)

1. Introduction

  • Judging the position of external objects relative to the body is essential for interacting with the external environment.
  • Both semicircular canals and otolith organs constantly provide afferent information regarding body orientation and body movement.
  • Here the authors aimed to clarify whether and how vestibular inputs contribute to egocentric spatial representation in healthy volunteers.
  • Perilymphatic cathodal currents depolarize the trigger site and lead to excitation, whereas anodal currents hyperpolarize it resulting in inhibition (Goldberg et al., 1984) .

2.1.2. Galvanic Vestibular Stimulation

  • Bipolar GVS was applied to deliver a boxcar pulse of 1 mA using a commercial stimulator (Good Vibrations Engineering Ltd., Nobleton, Ontario, Canada) .
  • Postural studies confirm that this level of GVS activates the vestibular organs without effects persisting beyond the period of stimulation (Fitzpatrick and Day, 2004) .
  • Carbon rubber electrodes (area 10 cm 2 ) coated with electrode gel were placed binaurally over the mastoid processes and fixed in place with adhesive tape.
  • Both left-anodal/right-cathodal (L-GVS) and right-anodal/left-cathodal (R-GVS) configurations were used (Fig. 1B ).
  • The authors also applied a sham stimulation using electrodes placed on the left and right side of the neck, about 5 cm below the GVS electrodes (Ferrè et al., 2013a , Ferrè et al., 2013b) , with a left-anodal/rightcathodal configuration.

2.1.2. Procedure

  • Verbal and written instructions were given to participants at the beginning of the session.
  • The participants' posture was monitored throughout the experiment to ensure that the body midline was always aligned with the center of the monitor.
  • The stimuli were shown 4 cm above the center of the monitor at the eye-line of the participants.
  • In the other half the hands were crossed so that the left hand pressed the right-sided button and vice versa (Fig. 1C ).
  • If the principal locus of GVS effects was to bias responding towards one hand, then performance on the localization task should be strongly affected by crossing the hands.

2.2. Results

  • Trials with implausibly short reaction times (< 183 ms: corresponding to 1 % of trials) were excluded from analysis.
  • The point of subjective equality (PSE) and just-noticeable difference (JND) were calculated from the functions for each participant in each condition.
  • The effect of GVS polarity was analyzed using a 2 (GVS polarity: L-GVS, R-GVS) x 2 (Hand posture: uncrossed, crossed) ANOVA.

2.3. Discussion

  • These results suggested that GVS changed the participants' egocentric spatial representation, with the perceived body midline shifting towards the anodal side.
  • There was no effect of crossing the hands, ruling out alternative explanations based on GVS affecting the selection or efficiency of lateralized motor output processes.
  • The authors data therefore support a body-related theory suggesting that GVS selectively modulates their egocentric spatial representations (Fig. 3A ).

3.1.2. Procedure

  • Thus, the task required a visual allocentric representation, centred on the reference, and egocentric location was irrelevant.
  • Peripheral presentation of the reference ensured that the task difficulty was equal between both experiments.
  • As there was no main effect of hand position in Experiment 1, participants completed this task with hands uncrossed.
  • The two reference locations (left and right) and three GVS polarities (L-GVS, R-GVS and sham stimulation) gave six conditions, repeated twice to give 12 blocks of 150 trials.
  • The experimental setup and all other procedures were as Experiment 1.

3.2. Results

  • The effect of GVS polarity was analyzed using a 2 (GVS polarity: L-GVS, R-GVS) x 2 (Reference: left, right) ANOVA.
  • The authors performed a two-way ANOVA with Stimulation (L-GVS and R-GVS) as within factor and Experiment (Exp.1 and Exp.2) as between factor.
  • These data indicate that GVS effect differ between experiments.
  • The authors subtracted Sham-GVS from R-GVS and L-GVS.

3.3. Discussion

  • GVS significantly biased allocentric visual localization in the opposite direction compared to the egocentric localization bias of Experiment 1 (Fig. 3D ).
  • This shift in attention would subsequently increase foveal mislocalisation for visual stimuli presented on the left, and reduce mislocalisation for stimuli on the right.
  • Hence, GVS biased allocentric representations towards the left for R-GVS and towards the right for L-GVS.
  • Taken together, their results highlight the relationship between vestibular information and egocentric body representation.
  • A final alternative explanation is that GVS could induce a change in gaze location which may have affected the egocentric judgement task.

Participants

  • None of the participants had participated in the previous experiments.
  • Exclusion criteria were as the previous experiments.

Procedure

  • Participants completed the egocentric localization task with GVS while their gaze location was recorded.
  • The task was completed with hands uncrossed.
  • Only L-GVS and R-GVS polarities were used.
  • The two conditions were repeated twice giving 4 blocks of 150 trials.
  • Gaze location was recorded with an Eyelink 2000 eye-tracker (sampling frequency 1 kHz).

4.1.2 Results

  • The PSE was shifted leftwards by 1.04 cm during L-GVS versus R-GVS, replicating the results of Experiment 1.
  • Eye-tracking data were processed by manual inspection and exclusion of trials with eye-blinks.
  • Figure 4B shows a fixation map, obtained from a representative participant.
  • Areas with longer fixation are shown with warmer colours (i.e. red).
  • Figure 4C shows the change in gaze location across time, averaged across participants.

4.2.2 Results

  • Figure 4D shows average PSEs across participants while gaze was directed either leftwards or rightwards.
  • The authors verified that the gaze was directed to the correct location by estimating the average gaze location during the period from the onset of the target to the response (mean ± SD: gaze-left = -3.9 ± 0.26 cm; gaze-right 4.0 ± 0.36 cm).

4.3. Discussion

  • The results of Experiment 3 showed that GVS can bias not only egocentric body representations (Fig. 4A ), but also shift horizontal gaze location (Fig. 4B ).
  • Thus, one might argue that this GVS-induced shift in gaze location could have indirectly driven the bias in egocentric body representation, without any direct effect of GVS.
  • In Experiment 4, egocentric judgements were not significantly altered when participants were explicitly asked to direct their gaze leftwards or rightwards by an amount equivalent to the GVS-induced bias (Fig. 4C ).
  • Taken together, these results therefore suggest that the indirect effect of GVS mediated by gaze shifts is minimal or absent.
  • Thus, the strong biasing effect of GVS on egocentric body representations is independent of changes in gaze location, and appears to represent a direct vestibular input to spatial representation of the body midline.

5. General Discussion

  • In many situations appropriate motor responses must be chosen rapidly based on the location of external objects relative to the body midline.
  • This bias has been successfully remediated by artificial vestibular stimulation, suggesting that the vestibular system contributes to body representation (Cappa et al., 1987; Vallar et al., 1993; Karnath et al., 1994) .
  • Thus, in Experiment 1, hand posture did not change the GVS effect on perceptual judgments (Fig. 2A and 2B), and there was no GVS effect on reaction times.
  • Voluntary gaze shift has been reported to modulate spatial representations (Cui et al., 2010) .
  • This seems to suggest that the representation of the midline is established by constant online integration of ongoing sensory input, rather than being a systematic stored knowledge about one's own body.

Did you find this useful? Give us your feedback

Citations
More filters
Journal Article

30 citations

Journal ArticleDOI
TL;DR: This work predicts that non-linear interactions across scales in hand movement series will produce variability that will actually stabilize aiming in the Fitts task, reducing standard deviation of target contacts and predicts the role of visual feedback in this case.
Abstract: Movement coordination depends on directing our limbs to the right place and in the right time. Movement science can study this central requirement in the Fitts task that asks participants to touch each of two targets in alternation, as accurately and as fast as they can. The Fitts task is an experimental attempt to focus on how the movement system balances its attention to speed and to accuracy. This balance in the Fitts task exhibits a hierarchical organization according to which finer details (e.g., kinematics of single sweeps from one target to the other) change with relatively broader constraints of task parameters (e.g., distance between targets and width of targets). The present work seeks to test the hypothesis that this hierarchical organization of movement coordination reflects a multifractal tensegrity in which non-linear interactions across scale support stability. We collected movement series data during a easy variant of the Fitts task to apply just such a multifractal analysis with surrogate comparison to allow clearer test of non-linear interactions across scale. Furthermore, we test the role of visual feedback both in potential and in fact, i.e., by manipulating both whether experimenters instructed participants that they might potentially have to close their eyes during the task and whether participants actually closed their eyes halfway through the task. We predict that (1) non-linear interactions across scales in hand movement series will produce variability that will actually stabilize aiming in the Fitts task, reducing standard deviation of target contacts; (2) non-linear interactions across scales in head sway will stabilize aiming following the actual closing eyes; and (3) non-linear interactions across scales in head sway and in hand movements will interact to support stabilizing effects of expectation about closing eyes. In sum, this work attempts to make the case that the multifractal-tensegrity hypothesis supports more accurate aiming behavior in the Fitts task.

23 citations


Cites background from "Disentangling the visual, motor and..."

  • ...Similarly, the strong relationships between the visual and vestibular systems (Abekawa et al., 2018; Ruhl et al., 2018) could explain these effects....

    [...]

Journal ArticleDOI
TL;DR: The physiotherapy interventions including neurodevelopmental treatment (NDT) and sensory integration (SI) helped in regaining locomotion ability in the child, who presented with difficulty to maintain sitting posture, and inability to stand and walk without support following viral encephalitis.
Abstract: Encephalitis refers to inflammation of the brain parenchyma It is potentially life-threatening with the highest incidence and severity in younger children Febrile infection-related epilepsy syndrome (FIRES) is a condition, in which a child develops a nonspecific febrile illness that may not persist when the initial seizure activity begins However, an electroencephalogram (EEG) shows that the child is in status epilepticus We report the case of a five-year-old male who presented with difficulty to maintain sitting posture, and inability to stand and walk without support, following viral encephalitis at the age of one year He had motor, visual, speech and cognitive impairment along with a seizure disorder The physiotherapy interventions including neurodevelopmental treatment (NDT) and sensory integration (SI) helped in regaining locomotion ability in the child The study aims to assess the impact of physiotherapy interventions on regaining locomotor ability in a child with FIRES following infective encephalitis

13 citations

Journal ArticleDOI
TL;DR: This study applied the misalignment paradigm in a perspective-taking task to investigate whether the weightings given to different body parts are shared across different spatial judgments involving different spatial axes.

4 citations

Journal ArticleDOI
TL;DR: In this article, the authors investigated whether vestibular inputs influence behavioral measurement of risk-taking propensity, and found that the effect depends on the GVS polarity of the vestibule, which preferentially activates the projections in the right hemisphere.

2 citations

References
More filters
Journal ArticleDOI
TL;DR: The literature suggests that tDCS and GVS are exciting and easily applicable research tools for neuropsychological as well as clinical-therapeutic investigations, and may induce neuroplastic changes which make them promising techniques in the field of neurorehabilitation.

453 citations

Journal ArticleDOI
01 Sep 1998-Brain
TL;DR: A PET activation study on CV was conducted and it was shown for the first time that visual motion stimulation with CV not only activates a medial parieto-occipital visual area bilaterally, separate from middle temporal/medial superior temporal areas, it also simultaneously deactivates the pariete-insular vestibular cortex.
Abstract: Summary The vestibular system—a sensor of head accelerations— cannot detect self-motion at constant velocity and thus requires supplementary visual information. The perception of self-motion during constant velocity movement is completely dependent on visually induced vection. This can be linear vection or circular vection (CV). CV is induced by large-field visual motion stimulation during which the stationary subject perceives the moving surroundings as being stable and himself as being moved. To determine the unknown cortical visual‐vestibular interaction during CV, we conducted a PET activation study on CV in 10 human volunteers. The PET images of cortical areas activated during visual motion stimulation without CV were compared with those with CV. Hitherto, CV was explained neurophysiologically by visual‐ vestibular convergence with activation of the vestibular nuclei, thalamic subnuclei and vestibular cortex. If CV were mediated by the vestibular cortex, one would expect

431 citations

Journal ArticleDOI
TL;DR: It is suggested that new insights into the neural basis of visual awareness may be gleaned from a different neuropsychological phenomenon, namely visual 'neglect' after injury to regions in the parietal lobe, which is consistent with recent data on single-cell activity in the monkey brain.
Abstract: The last decade has seen a resurgence of interest in the neural correlates of conscious vision, with most discussion focused on the 'blindsight' that can follow damage to primary visual cortex, in the occipital lobe. We suggest that new insights into the neural basis of visual awareness may be gleaned from a different neuropsychological phenomenon, namely visual 'neglect' after injury to regions in the parietal lobe. Neglect provides several revealing contrasts with occipital blindsight. Here we summarise four key findings. First, unlike the deficits caused by damage to primary visual cortex, the loss of awareness in parietal neglect is characteristically not strictly retinotopic. Second, visual segmentation processes are preserved in neglect, and can influence what will reach the patient's awareness. Third, extensive unconscious processing takes place for those stimuli on the neglected side which escape awareness, including some degree of object identification. Finally, parietal damage affects initial stages of motor planning as well as perception. These findings are consistent with recent data on single-cell activity in the monkey brain. They also suggest why areas in the inferior parietal lobe may play a prominent role in visual awareness.

415 citations

Journal ArticleDOI
TL;DR: Stimulus-dependent, inhibitory vestibular-visual, and nociceptive-somatosensory interactions may be functionally significant for processing perception and sensorimotor control.
Abstract: Functional magnetic resonance imaging blood-oxygenation-level-dependent (BOLD) signal increases (activations) and BOLD signal decreases (“deactivations”) were compared in six healthy volunteers dur...

400 citations

Journal Article
01 Jan 1998-Nature
TL;DR: This paper found that visual segmentation processes are preserved in neglect, and extensive unconscious processing takes place for those stimuli on the neglected side which escape awareness, including some degree of object identification.
Abstract: The last decade has seen a resurgence of interest in the neural correlates of conscious vision, with most discussion focused on the 'blindsight' that can follow damage to primary visual cortex, in the occipital lobe. We suggest that new insights into the neural basis of visual awareness may be gleaned from a different neuropsychological phenomenon, namely visual 'neglect' after injury to regions in the parietal lobe. Neglect provides several revealing contrasts with occipital blindsight. Here we summarise four key findings. First, unlike the deficits caused by damage to primary visual cortex, the loss of awareness in parietal neglect is characteristically not strictly retinotopic. Second, visual segmentation processes are preserved in neglect, and can influence what will reach the patient's awareness. Third, extensive unconscious processing takes place for those stimuli on the neglected side which escape awareness, including some degree of object identification. Finally, parietal damage affects initial stages of motor planning as well as perception. These findings are consistent with recent data on single-cell activity in the monkey brain. They also suggest why areas in the inferior parietal lobe may play a prominent role in visual awareness.

395 citations