Mal de Debarquement Syndrome explained by a vestibulo–cerebellar oscillator

Author:

Burlando Bruno1,Mucci Viviana2,Browne Cherylea J23,Losacco Serena1,Indovina Iole45,Marinelli Lucio67,Blanchini Franco8,Giordano Giulia9

Affiliation:

1. University of Genova Department of Pharmacy, , Viale Benedetto XV 3, 16132 Genova, Italy

2. Western Sydney University School of Science, , Penrith NSW 2560, Australia

3. UNSW Sydney Translational Neuroscience Facility, School of Medical Sciences, , NSW 2052, Australia

4. University of Messina Department of Biomedical and Dental Sciences and Morphofunctional Imaging, , 98125 Messina, Italy

5. IRCCS Foundation Santa Lucia Neuromotor Physiology Lab, , via Ardeatina 354, 00179 Rome, Italy

6. University of Genova DINOGMI , Largo Daneo 3, 16132, Genova, Italy

7. IRCCS Ospedale Policlinico San Martino , Division of Clinical Neurophysiology, Department of Neuroscience, Largo R. Benzi 10, 16132 Genova, Italy

8. University of Udine Department of Mathematics, Computer Science and Physics, , Via delle Scienze 208, 33100 Udine, Italy

9. University of Trento Department of Industrial Engineering, , Via Sommarive 9, 38123 Povo (TN), Italy

Abstract

AbstractMal 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.

Publisher

Oxford University Press (OUP)

Subject

Applied Mathematics,Pharmacology,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Modeling and Simulation,General Medicine,General Neuroscience

Reference43 articles.

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