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

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 si...

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Veröffentlicht in:Journal of neurochemistry 2003-07, Vol.86 (1), p.267-272
Hauptverfasser: Klivenyi, Peter, Ferrante, Robert J., Gardian, Gabrielle, Browne, Susan, Chabrier, Pierre‐Etienne, Beal, M. Flint
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Sprache:eng
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Zusammenfassung: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.
ISSN:0022-3042
1471-4159
DOI:10.1046/j.1471-4159.2003.t01-1-01868.x