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Neurobiol Dis ; 40(1): 82-92, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20483372

RESUMO

The mechanisms underlying neuron death in Parkinson's disease are unknown, but both genetic defects and environmental factors are implicated in its pathogenesis. Mutations in the parkin gene lead to autosomal recessive juvenile Parkinsonism (AR-JP). Here we report that compared to control flies, Drosophila lacking parkin show significantly reduced lifespan but no difference in dopamine neuron numbers when raised on food supplemented with environmental pesticides or mitochondrial toxins. Moreover, chelation of redox-active metals, anti-oxidants and overexpression of superoxide dismutase 1 all significantly reversed the reduced longevity of parkin-deficient flies. Finally, parkin deficiency exacerbated the rough eye phenotype of Drosophila caused by overexpression of the copper importer B (Ctr1B). Taken together, our results demonstrate an important function of parkin in the protection against redox-active metals and pesticides implicated in the etiology of Parkinson's disease. They also corroborate that oxidative stress, perhaps as a consequence of mitochondrial dysfunction, is a major determinant of morbidity in parkin mutant flies.


Assuntos
Sistema Nervoso Central/metabolismo , Proteínas de Drosophila/deficiência , Drosophila melanogaster/genética , Longevidade/genética , Mutação/genética , Neurônios/metabolismo , Ubiquitina-Proteína Ligases/deficiência , Animais , Sistema Nervoso Central/efeitos dos fármacos , Modelos Animais de Doenças , Proteínas de Drosophila/genética , Longevidade/efeitos dos fármacos , Neurônios/efeitos dos fármacos , Doença de Parkinson/genética , Doença de Parkinson/metabolismo , Ubiquitina-Proteína Ligases/genética
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