Increased survival and neuroprotective effects of BN82451 in a transgenic mouse model of Huntington's disease

P Klivenyi, RJ Ferrante, G Gardian… - Journal of …, 2003 - Wiley Online Library
P Klivenyi, RJ Ferrante, G Gardian, S Browne, PE Chabrier, MF Beal
Journal of neurochemistry, 2003Wiley Online Library
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 …
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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