A Perspective for Ménière's Disease: In Silico Investigations of Dexamethasone as a Direct Modulator of AQP2.

Ménière’s disease dexamethasone human AQP2 molecular dynamics water channel water permeability modulation

Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
28 03 2022
Historique:
received: 03 03 2022
revised: 21 03 2022
accepted: 24 03 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 27 4 2022
Statut: epublish

Résumé

Ménière's disease is a chronic illness characterized by intermittent episodes of vertigo associated with fluctuating sensorineural hearing loss, tinnitus and aural pressure. This pathology strongly correlates with a dilatation of the fluid compartment of the endolymph, so-called hydrops. Dexamethasone is one of the therapeutic approaches recommended when conventional antivertigo treatments have failed. Several mechanisms of actions have been hypothesized for the mode of action of dexamethasone, such as the anti-inflammatory effect or as a regulator of inner ear water homeostasis. However, none of them have been experimentally confirmed so far. Aquaporins (AQPs) are transmembrane water channels and are hence central in the regulation of transcellular water fluxes. In the present study, we investigated the hypothesis that dexamethasone could impact water fluxes in the inner ear by targeting AQP2. We addressed this question through molecular dynamics simulations approaches and managed to demonstrate a direct interaction between AQP2 and dexamethasone and its significant impact on the channel water permeability. Through compartmentalization of sodium and potassium ions, a significant effect of Na+ upon AQP2 water permeability was highlighted as well. The molecular mechanisms involved in dexamethasone binding and in its regulatory action upon AQP2 function are described.

Identifiants

pubmed: 35454100
pii: biom12040511
doi: 10.3390/biom12040511
pmc: PMC9028334
pii:
doi:

Substances chimiques

AQP2 protein, human 0
Aquaporin 2 0
Water 059QF0KO0R
Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Robin Mom (R)

Research Group on Vestibular Pathophysiology, CNRS, Unit GDR2074, F-13331 Marseille, France.

Julien Robert-Paganin (J)

Structural Motility, Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS UMR144, F-75005 Paris, France.

Thierry Mom (T)

Research Group on Vestibular Pathophysiology, CNRS, Unit GDR2074, F-13331 Marseille, France.
Service d'ORL et de Chirurgie Cervicofaciale, Hôpital Gabriel Montpied, F-63003 Clermont-Ferrand, France.
Unité Mixte de Recherche (UMR) 1107 Neurodol, INSERM, F-63003 Clermont-Ferrand, France.

Christian Chabbert (C)

Research Group on Vestibular Pathophysiology, CNRS, Unit GDR2074, F-13331 Marseille, France.
Aix Marseille University-CNRS, Laboratory of Cognitive Neurosciences, Team Pathophysiology and Therapy of Vestibular Disorders, UMR7291, F-13331 Marseille, France.

Stéphane Réty (S)

Laboratoire de Biologie et Modélisation de la Cellule, ENS de Lyon, University Claude Bernard, CNRS UMR 5239, INSERM U1210, 46 Allée d'Italie Site Jacques Monod, F-69007 Lyon, France.

Daniel Auguin (D)

Structural Motility, Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS UMR144, F-75005 Paris, France.
Laboratoire de Biologie des Ligneux et des Grandes Cultures, Université d'Orléans, UPRES EA 1207, INRA-USC1328, F-45067 Orléans, France.

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