Neuronal cell death in Huntington's disease: a potential role for dopamine.

Abstract:

:Huntington's disease is an inherited neurodegenerative disorder, the cause of which is unknown. Excitotoxicity, mitochondrial dysfunction and oxidative stress are all likely to contribute to the striatal cell death that occurs in this disorder. There are accumulating data indicating that under specific circumstances, dopamine, which occurs in high concentrations in the basal ganglia, might be neurotoxic. In this article, the current models used to study Huntington's disease are reviewed and the recent findings that implicate dopamine in the pathophysiology of this progressive disorder are discussed. Although many questions remain unanswered, the dopaminergic system could contribute to striatal vulnerability in Huntington's disease and provide a novel avenue for the development of new therapies.

journal_name

Trends Neurosci

journal_title

Trends in neurosciences

authors

Jakel RJ,Maragos WF

doi

10.1016/s0166-2236(00)01568-x

subject

Has Abstract

pub_date

2000-06-01 00:00:00

pages

239-45

issue

6

eissn

0166-2236

issn

1878-108X

pii

S0166-2236(00)01568-X

journal_volume

23

pub_type

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