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Multisensory gamma stimulation mitigates the effects of demyelination induced by cuprizone in male mice

Authors :
Daniela Rodrigues-Amorim
P. Lorenzo Bozzelli
TaeHyun Kim
Liwang Liu
Oliver Gibson
Cheng-Yi Yang
Mitchell H. Murdock
Fabiola Galiana-Melendez
Brooke Schatz
Alexis Davison
Md Rezaul Islam
Dong Shin Park
Ravikiran M. Raju
Fatema Abdurrob
Alissa J. Nelson
Jian Min Ren
Vicky Yang
Matthew P. Stokes
Li-Huei Tsai
Source :
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

Abstract Demyelination is a common pathological feature in a wide range of diseases, characterized by the loss of myelin sheath and myelin-supporting oligodendrocytes. These losses lead to impaired axonal function, increased vulnerability of axons to damage, and result in significant brain atrophy and neuro-axonal degeneration. Multiple pathomolecular processes contribute to neuroinflammation, oligodendrocyte cell death, and progressive neuronal dysfunction. In this study, we use the cuprizone mouse model of demyelination to investigate long-term non-invasive gamma entrainment using sensory stimulation as a potential therapeutic intervention for promoting myelination and reducing neuroinflammation in male mice. Here, we show that multisensory gamma stimulation mitigates demyelination, promotes oligodendrogenesis, preserves functional integrity and synaptic plasticity, attenuates oligodendrocyte ferroptosis-induced cell death, and reduces brain inflammation. Thus, the protective effects of multisensory gamma stimulation on myelin and anti-neuroinflammatory properties support its potential as a therapeutic approach for demyelinating disorders.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.8ebed6b59c0b464ab74100e9c4457c3e
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-024-51003-7