2015, Number 2
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Rev Cubana Invest Bioméd 2015; 34 (2)
Glutathione antioxidant system in the etiopathology of nigrostriatal dysfunction
Díaz-Hung ML, González FME, Blanco LL
Language: Spanish
References: 67
Page: 168-186
PDF size: 328.15 Kb.
ABSTRACT
Parkinson’s disease is a chronic neurodegenerative condition affecting elderly persons.
In a minority of cases the disease has a genetic origin, but in most the cause is
idiopathic. Accumulation of free radicals and loss of glutathione homeostasis have
been pointed at as possible causal agents. The purpose of the study was to review
experimental evidence supporting the involvement of free radicals and loss of
glutathione homeostasis in the outset and progress of
substantia nigra pars compacta
degeneration. Oxidative stress in Parkinson’s disease may be related to the intrinsic
pro-oxidant properties of dopamine and high iron concentrations in the
substantia
nigra pars compacta, promoting dopamine oxidation and the generation of reactive
oxygen species. Any event triggering these mechanisms will cause cell damage.
Glutathione reduction is one of the earliest biochemical alterations detected in
association with Parkinson’s disease, and it has been related to the inhibition of
complex I of the mitochondrial transport chain, oxidative damage and glial activation,
among other factors leading to neurodegeneration. This evidence points to the need
to maintain glutathione homeostasis in the dopaminergic system, as well as its
relationship to the etiology of nigrostriatal degeneration, of potential application in
clinical practice.
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