Mal de Debarquement Syndrome explained by a vestibulo-cerebellar oscillator

Journal Article (2023)
Author(s)

Bruno Burlando (Università degli Studi di Genova)

Viviana Mucci (Western Sydney University)

Cherylea J. Browne (Western Sydney University, University of New South Wales, Australia)

Serena Losacco (Università degli Studi di Genova)

Iole Indovina (Istituto di Ricovero e Cura a Carattere Scientifico Fondazione Santa Lucia, University of Messina)

Lucio Marinelli (Istituto Italiano di Tee-nologia, Università degli Studi di Genova)

Franco Blanchini (Università degli Studi di Udine)

Giulia Giordano (Università degli Studi di Trento)

DOI related publication
https://doi.org/10.1093/imammb/dqac016 Final published version
More Info
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Publication Year
2023
Language
English
Issue number
1
Volume number
40
Pages (from-to)
96-110
Downloads counter
295

Abstract

Mal de Debarquement Syndrome (MdDS) is a puzzling central vestibular disorder characterized by a long-lasting perception of oscillatory postural instability that may occur after sea travels or flights. We have postulated that MdDS originates from the post-disembarking persistence of an adaptive internal oscillator consisting of a loop system, involving the right and left vestibular nuclei, and the Purkinje cells of the right and left flocculonodular cerebellar cortex, connected by GABAergic and glutamatergic fibers. We have formulated here a mathematical model of the vestibulo-cerebellar loop system and carried out a computational analysis based on a set of differential equations describing the interactions among the loop elements and containing Hill functions that model input-output firing rates relationships among neurons. The analysis indicates that the system acquires a spontaneous and permanent oscillatory behavior for a decrease of threshold and an increase of sensitivity in neuronal input-output responses. These results suggest a role for synaptic plasticity in MdDS pathophysiology, thus reinforcing our previous hypothesis that MdDS may be the result of excessive synaptic plasticity acting on the vestibulo-cerebellar network during its entraining to an oscillatory environment. Hence, our study points to neuroendocrine pathways that lead to increased synaptic response as possible new therapeutic targets for the clinical treatment of the disorder.