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Vestibular prepulse inhibition of the human blink reflex

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Abstract Objective Auditory and somatosensory prepulses are commonly used to assess prepulse inhibition (PPI). The effect of a vestibular prepulse upon blink reflex (BR) excitability has not been hitherto assessed. Methods Twenty-two healthy subjects and two patients with bilateral peripheral vestibular failure took part in the study. Whole body yaw rotation in the dark provided a vestibular inertial prepulse. BR was electrically evoked after the end of the rotation. The area-under-the-curve (area) of the BR responses (R1, R2, and R2c) was recorded and analysed. Results A vestibular prepulse inhibited the R2 (p < 0.001) and R2c area (p < 0.05). Increasing the angular acceleration did not increase the R2/R2c inhibition (p>0.05). Voluntary suppression of the vestibular-ocular reflex did not affect the magnitude of inhibition (p>0.05). Patients with peripheral vestibular failure did not show any inhibition. Conclusions Our data support a vestibular-gating mechanism in humans. Significance The main brainstem nucleus mediating PPI – the pedunculopontine nucleus (PPN) – is heavily vestibular responsive, which is consistent with our findings of a vestibular-mediated PPI. Our technique may be used to interrogate the fidelity of brain circuits mediating vestibular-related PPN functions. Given the PPN’s importance in human postural control, our technique may also provide a neurophysiological biomarker of balance. Highlights This is the first report of a vestibular prepulse inhibition of the blink reflex. A vestibular prepulse inhibits the R2/R2c area in healthy subjects but not in patients with bilateral peripheral vestibular failure. Vestibular PPI is a potential neurophysiological marker of vestibular-motor integration at the brainstem level.
Title: Vestibular prepulse inhibition of the human blink reflex
Description:
Abstract Objective Auditory and somatosensory prepulses are commonly used to assess prepulse inhibition (PPI).
The effect of a vestibular prepulse upon blink reflex (BR) excitability has not been hitherto assessed.
Methods Twenty-two healthy subjects and two patients with bilateral peripheral vestibular failure took part in the study.
Whole body yaw rotation in the dark provided a vestibular inertial prepulse.
BR was electrically evoked after the end of the rotation.
The area-under-the-curve (area) of the BR responses (R1, R2, and R2c) was recorded and analysed.
Results A vestibular prepulse inhibited the R2 (p < 0.
001) and R2c area (p < 0.
05).
Increasing the angular acceleration did not increase the R2/R2c inhibition (p>0.
05).
Voluntary suppression of the vestibular-ocular reflex did not affect the magnitude of inhibition (p>0.
05).
Patients with peripheral vestibular failure did not show any inhibition.
Conclusions Our data support a vestibular-gating mechanism in humans.
Significance The main brainstem nucleus mediating PPI – the pedunculopontine nucleus (PPN) – is heavily vestibular responsive, which is consistent with our findings of a vestibular-mediated PPI.
Our technique may be used to interrogate the fidelity of brain circuits mediating vestibular-related PPN functions.
Given the PPN’s importance in human postural control, our technique may also provide a neurophysiological biomarker of balance.
Highlights This is the first report of a vestibular prepulse inhibition of the blink reflex.
A vestibular prepulse inhibits the R2/R2c area in healthy subjects but not in patients with bilateral peripheral vestibular failure.
Vestibular PPI is a potential neurophysiological marker of vestibular-motor integration at the brainstem level.

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