4.7 Article

Repetitive Low-Intensity Vestibular Noise Stimulation Partly Reverses Behavioral and Brain Activity Changes following Bilateral Vestibular Loss in Rats

Journal

BIOMOLECULES
Volume 13, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/biom13111580

Keywords

bilateral vestibulopathy; galvanic vestibular stimulation; stochastic resonance; F-18-FDG imaging; locomotion; gait ataxia

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This study investigates the neurophysiological and neuroanatomical mechanisms underlying the therapeutic effects of low-intensity noisy galvanic vestibular stimulation (nGVS) on postural deficits in patients with bilateral vestibular loss (BVL). The results demonstrate that nGVS modulates regional brain activation patterns and improves posture deficits in BVL patients, particularly in the early stages of recovery. The study also reveals the link between stimulation-induced locomotor improvements and brain activity responses.
Low-intensity noisy galvanic vestibular stimulation (nGVS) can improve static and dynamic postural deficits in patients with bilateral vestibular loss (BVL). In this study, we aimed to explore the neurophysiological and neuroanatomical substrates underlying nGVS treatment effects in a rat model of BVL. Regional brain activation patterns and behavioral responses to a repeated 30 min nGVS treatment in comparison to sham stimulation were investigated by serial whole-brain F-18-FDG-PET measurements and quantitative locomotor assessments before and at nine consecutive time points up to 60 days after the chemical bilateral labyrinthectomy (BL). The F-18-FDG-PET revealed a broad nGVS-induced modulation on regional brain activation patterns encompassing biologically plausible brain networks in the brainstem, cerebellum, multisensory cortex, and basal ganglia during the entire observation period post-BL. nGVS broadly reversed brain activity adaptions occurring in the natural course post-BL. The parallel behavioral locomotor assessment demonstrated a beneficial treatment effect of nGVS on sensory-ataxic gait alterations, particularly in the early stage of post-BL recovery. Stimulation-induced locomotor improvements were finally linked to nGVS brain activity responses in the brainstem, hemispheric motor, and limbic networks. In conclusion, combined F-18-FDG-PET and locomotor analysis discloses the potential neurophysiological and neuroanatomical substrates that mediate previously observed therapeutic nGVS effects on postural deficits in patients with BVL.

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