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L-dihydroxyphenylalanine and complex I deficiency in Parkinson's disease brain.
Cooper, J M; Daniel, S E; Marsden, C D; Schapira, A H.
Afiliação
  • Cooper JM; Department of Clinical Neurosciences, Royal Free Hospital School of Medicine, London, England, U.K.
Mov Disord ; 10(3): 295-7, 1995 May.
Article em En | MEDLINE | ID: mdl-7651446
There is evidence for a 37% deficiency of complex I activity in Parkinson's disease (PD), which appears to be specific for PD amongst parkinsonian syndromes and selective for the substantia nigra within the central nervous system. Rat studies have shown that, in the context of a normal nigrostriatal dopaminergic cell population, L-dihydroxyphenylalanine (L-dopa) causes a reversible 25% defect of complex I activity in nigral and striatal tissue. Analysis of striatal tissue from PD patients after prolonged exposure to high-dose L-dopa does not show such a defect. Results of these and other studies suggest that L-dopa therapy does not cause complex I deficiency in PD striatum. However, it cannot be excluded that, in the particular environment of the PD substantia nigra, L-dopa may enhance a preexisting complex I defect.
Assuntos
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Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Encéfalo / Levodopa / NAD(P)H Desidrogenase (Quinona) Idioma: En Revista: Mov Disord Ano de publicação: 1995 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Encéfalo / Levodopa / NAD(P)H Desidrogenase (Quinona) Idioma: En Revista: Mov Disord Ano de publicação: 1995 Tipo de documento: Article