Abstract
There is substantial evidence that excitotoxicity and oxidative damage may contribute to Huntington's disease (HD) pathogenesis. We examined whether the novel anti-oxidant compound BN82451 exerts neuroprotective effects in the R6/2 transgenic mouse model of HD. Oral administration of BN82451 significantly improved motor performance and improved survival by 15%. Oral administration of BN82451 significantly reduced gross brain atrophy, neuronal atrophy and the number of neuronal intranuclear inclusions at 90 days of age. These findings provide evidence that novel anti-oxidants such as BN82451 may be useful for treating HD.
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Klivenyi, P., Ferrante, R. J., Gardian, G., Browne, S., Chabrier, P. E., & Beal, M. F. (2003). Increased survival and neuroprotective effects of BN82451 in a transgenic mouse model of Huntington’s disease. Journal of Neurochemistry, 86(1), 267–272. https://doi.org/10.1046/j.1471-4159.2003.t01-1-01868.x
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