Hydrogen Sulfide Alleviates Demyelination, Behavioral and Motor Impairments in a Cuprizone-Induced Rat Model of Multiple Sclerosis
DOI:
10.1007/s44411-025-00129-1
Publication Date:
2025-04-08T04:48:42Z
AUTHORS (3)
ABSTRACT
Abstract
Objectives
This study investigated the effects of the H2S donor sodium hydrosulfide (NaHS) on demyelination and behavioral deficits in a cuprizone (CPZ)-induced experimental rat model of MS.
Methods
The rats were fed chow pellets supplemented with 1% CPZ for 5 weeks, and NaHS (50 and 100 μmol/kg) was administered during the last 2 weeks. For behavioral assessment, grip strength, passive avoidance, rota rod and elevated plus maze tests were performed. Nuclear factor kappa-B (NF-κB) and interleukin-1 beta (IL-1β) were measured to assess inflammation in brain tissue. Demyelination in the corpus callosum (CC) was assessed by immunohistochemistry for myelin basic protein (MBP), platelet-derived growth factor receptor α (PDGFRα) and Glial fibrillary acidic protein (GFAP). The TUNEL method was used to assess apoptosis.
Results
Demyelination in the CC was reduced in the NaHS-treated groups. NaHS increased the amount of MBP and decreased the amount of PDGFRα and GFAP immunoreactive cells. NaHS reduced NF-κB, IL-1β levels, and the number of apoptotic cells in the brain tissue. In addition, NaHS improved muscle strength, motor coordination, learning and memory, and showed a significant anxiolytic effect. However, it was found that the beneficial effects of NaHS decreased at a high dose of 100 μmol/kg.
Conclusion
H2S showed neuroprotective effects by reducing demyelination, inflammation and apoptosis in the CPZ-induced MS model. H2S also improved muscle strength, motor coordination, learning and memory and showed anxiolytic activity. Anti-inflammatory, anti-apoptotic and antioxidant effects may play a role in the neuroprotective effects of H2S.
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