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The role of glutathione in dopaminergic neuronal survival.
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An increased production of reactive oxygen species is thought to be
critical to the pathogenesis of Parkinson's disease.

At autopsy, patients with either presymptomatic or symptomatic Parkinson's
disease have a decreased level of glutathione in the substantia nigra pars
compacta.

This change represents the earliest index of oxidative stress in
Parkinson's disease discovered to this point.

This study compares the sensitivity of dopaminergic and nondopaminergic
neurons in dissociated mesencephalic cultures to the depletion of glutathione.

We have found that dopaminergic neurons are more resistant to the toxicity
of glutathione depletion than nondopaminergic neurons.

The possibility that dopaminergic neurons have a higher baseline
glutathione level than nondopaminergic neurons is suggested by measurements
of levels of cellular glutathione in a parallel system of immortalized
embryonic dopaminergic and nondopaminergic cell lines.

We also examined the role of glutathione in 1-methyl-4-phenylpyridinium
toxicity.
Decreasing the glutathione level of dopaminergic neurons potentiates their
susceptibility to 1-methyl-4-phenylpyridinium toxicity, although
1-methyl-4-phenylpyridinium does not deplete glutathione from primary
mesencephalic cultures.

Our data suggest that although a decreased glutathione content is not
likely to be the sole cause of dopaminergic neuronal loss in Parkinson's
disease, decreased glutathione content may act in conjunction with other
factors such as 1-methyl-4-phenylpyridinium to cause the selective death of
dopaminergic neurons.


J Neurochem 1997 Nov;69(5):1850-1858
Nakamura K, Wang W, Kang UJ
University of Chicago, Illinois 60637, U.S.A.
PMID: 9349527, MUID: 98007683
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