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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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Bibliografske podrobnosti
Main Authors: Canzoniero, Lorella M. T., Granzotto, Alberto, Turetsky, Dorothy M., Choi, Dennis W., Dugan, Laura L., Sensi, Stefano L.
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2013
Teme:
Online dostop: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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