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Fullerenols Prevent Neuron Death and Reduce Oxidative Stress in Drosophila Huntington's Disease Model.

Olga I BolshakovaAlina A BorisenkovaIlya M GolomidovArtem E KomissarovAlexandra D SlobodinaElena V RyabovaIrina S RyabokonEvgenia M LatypovaElizaveta E SlepnevaSvetlana V Sarantseva
Published in: Cells (2022)
Huntington's disease (HD) is one of the human neurodegenerative diseases for which there is no effective treatment. Therefore, there is a strong demand for a novel neuroprotective agent that can alleviate its course. Fullerene derivatives are considered to be such agents; however, they need to be comprehensively investigated in model organisms. In this work, neuroprotective activity of C 60 (OH) 30 and C 120 O(OH) 44 fullerenols was analyzed for the first time in a Drosophila transgenic model of HD. Lifespan, behavior, oxidative stress level and age-related neurodegeneration were assessed in flies with the pathogenic Huntingtin protein expression in nerve cells. Feed supplementation with hydroxylated C 60 fullerene and C 120 O dimer oxide molecules was shown to diminish the oxidative stress level and neurodegenerative processes in the flies' brains. Thus, fullerenes displayed neuroprotective activity in this model.
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