Multisensory gamma stimulation mitigates the effects of demyelination induced by cuprizone in male mice.
Daniela Rodrígues-AmorímP Lorenzo BozzelliTaeHyun KimLiwang LiuOliver GibsonCheng-Yi YangMitchell H MurdockFabiola Galiana-MelendezBrooke SchatzAlexis DavisonMd Rezaul IslamDong Shin ParkRavikiran M RajuFatema AbdurrobAlissa J NelsonJian Min RenVicky YangMatthew P StokesLi-Huei TsaiPublished in: Nature communications (2024)
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.
Keyphrases
- cell death
- white matter
- cerebral ischemia
- oxidative stress
- mouse model
- multiple sclerosis
- spinal cord injury
- traumatic brain injury
- cell cycle arrest
- resting state
- cognitive impairment
- lps induced
- machine learning
- climate change
- diabetic rats
- deep learning
- radiation induced
- blood brain barrier
- cell proliferation
- high glucose