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nNOS(+) striatal neurons, a subpopulation spared in Huntington's Disease, possess functional NMDA receptors but fail to generate mitochondrial ROS in response to an excitotoxic challenge

Huntington's disease (HD) is a neurodegenerative condition characterized by severe neuronal loss in the cortex and striatum that leads to motor and behavioral deficits. Excitotoxicity is thought to be involved in HD and several studies have indicated that NMDA receptor (NMDAR) overactivation ca...

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Detalhes bibliográficos
Main Authors: Canzoniero, Lorella M. T., Granzotto, Alberto, Turetsky, Dorothy M., Choi, Dennis W., Dugan, Laura L., Sensi, Stefano L.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3655281/
https://ncbi.nlm.nih.gov/pubmed/23720635
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2013.00112
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