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

Daniela Rodrígues-Amorím(Massachusetts Institute of Technology), P. Lorenzo Bozzelli(Massachusetts Institute of Technology), TaeHyun Kim(Massachusetts Institute of Technology), Liwang Liu(Massachusetts Institute of Technology), Oliver Gibson, Cheng-Yi Yang(Massachusetts Institute of Technology), Mitchell H. Murdock(Massachusetts Institute of Technology), Fabiola Galiana-Melendez(Massachusetts Institute of Technology), Brooke Schatz(Massachusetts Institute of Technology), Alexis Davison(Massachusetts Institute of Technology), Md. Rezaul Islam(Massachusetts Institute of Technology), Dong Shin Park(Massachusetts Institute of Technology), Ravikiran M. Raju(Boston Children's Hospital), Fatema Abdurrob(Massachusetts Institute of Technology), Alissa J. Nelson(Cell Signaling Technology (United States)), Jinqi Ren(Cell Signaling Technology (United States)), Vicky K. Yang(Cell Signaling Technology (United States)), Matthew P. Stokes(Cell Signaling Technology (United States)), Li‐Huei Tsai(Broad Institute)
Nature Communications
August 8, 2024
Cited by 21Open Access
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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. Demyelination leads to nerve damage and inflammation. Here, the authors show multisensory gamma stimulation’s potential to mitigate demyelination and neuroinflammation, suggesting that this might be a therapeutic strategy for demyelinating diseases.


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