» Articles » PMID: 37889571

Electrical Stimulation of the Peripheral and Central Vestibular System

Overview
Specialty Neurology
Date 2023 Oct 27
PMID 37889571
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: Electrical stimulation of the peripheral and central vestibular system using noninvasive (galvanic vestibular stimulation, GVS) or invasive (intracranial electrical brain stimulation, iEBS) approaches have a long history of use in studying self-motion perception and balance control. The aim of this review is to summarize recent electrophysiological studies of the effects of GVS, and functional mapping of the central vestibular system using iEBS in awake patients.

Recent Findings: The use of GVS has become increasingly common in the assessment and treatment of a wide range of clinical disorders including vestibulopathy and Parkinson's disease. The results of recent single unit recording studies have provided new insight into the neural mechanisms underlying GVS-evoked improvements in perceptual and motor responses. Furthermore, the application of iEBS in patients with epilepsy or during awake brain surgery has provided causal evidence of vestibular information processing in mostly the middle cingulate cortex, posterior insula, inferior parietal lobule, amygdala, precuneus, and superior temporal gyrus.

Summary: Recent studies have established that GVS evokes robust and parallel activation of both canal and otolith afferents that is significantly different from that evoked by natural head motion stimulation. Furthermore, there is evidence that GVS can induce beneficial neural plasticity in the central pathways of patients with vestibular loss. In addition, iEBS studies highlighted an underestimated contribution of areas in the medial part of the cerebral hemispheres to the cortical vestibular network.

Citing Articles

Brain Functional Alterations in Patients With Benign Paroxysmal Positional Vertigo Demonstrate the Visual-Vestibular Interaction and Integration.

Wu J, Shu L, Zhou C, Du X, Sun X, Pan H Brain Behav. 2024; 14(10):e70053.

PMID: 39350430 PMC: 11442312. DOI: 10.1002/brb3.70053.


Vertiginous epilepsy in the pediatric population.

Wood A, Thompson-Harvey A, Kesser B Front Neurol. 2024; 15:1403536.

PMID: 39036629 PMC: 11259007. DOI: 10.3389/fneur.2024.1403536.


Exploring physiological stress response evoked by passive translational acceleration in healthy adults: a pilot study utilizing electrodermal activity and heart rate variability measurements.

Yu X, Lu J, Liu W, Cheng Z, Xiao G Sci Rep. 2024; 14(1):11349.

PMID: 38762532 PMC: 11102551. DOI: 10.1038/s41598-024-61656-5.


Appropriate Vestibular Stimulation in Children and Adolescents-A Prerequisite for Normal Cognitive, Motor Development and Bodily Homeostasis-A Review.

Bozanic Urbancic N, Battelino S, Vozel D Children (Basel). 2024; 11(1).

PMID: 38275423 PMC: 10814320. DOI: 10.3390/children11010002.

References
1.
Gensberger K, Kaufmann A, Dietrich H, Branoner F, Banchi R, Chagnaud B . Galvanic Vestibular Stimulation: Cellular Substrates and Response Patterns of Neurons in the Vestibulo-Ocular Network. J Neurosci. 2016; 36(35):9097-110. PMC: 6601907. DOI: 10.1523/JNEUROSCI.4239-15.2016. View

2.
Raiser T, Flanagin V, Duering M, van Ombergen A, Ruehl R, Zu Eulenburg P . The human corticocortical vestibular network. Neuroimage. 2020; 223:117362. DOI: 10.1016/j.neuroimage.2020.117362. View

3.
Cullen K . Vestibular processing during natural self-motion: implications for perception and action. Nat Rev Neurosci. 2019; 20(6):346-363. PMC: 6611162. DOI: 10.1038/s41583-019-0153-1. View

4.
Stephan T, Hufner K, Brandt T . Stimulus profile and modeling of continuous galvanic vestibular stimulation in functional magnetic resonance imaging. Ann N Y Acad Sci. 2009; 1164:472-5. DOI: 10.1111/j.1749-6632.2008.03715.x. View

5.
Harroud A, Boucher O, Tran T, Harris L, Hall J, Dubeau F . Precuneal epilepsy: Clinical features and surgical outcome. Epilepsy Behav. 2017; 73:77-82. DOI: 10.1016/j.yebeh.2017.05.018. View