Please use this identifier to cite or link to this item:
Type: Artigo
Title: Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia
Author: Melo, Daniela R
Kowaltowski, Alicia J
Wajner, Moacir
Castilho, Roger F
Abstract: Methylmalonic acidemia is one of the most prevalent inherited metabolic disorders involving neurological deficits. In vitro experiments, animal model studies and tissue analyses from human patients suggest extensive impairment of mitochondrial energy metabolism in this disease. This review summarizes changes in mitochondrial energy metabolism occurring in methylmalonic acidemia, focusing mainly on the effects of accumulated methylmalonic acid, and gives an overview of the results found in different experimental models. Overall, experiments to date suggest that mitochondrial impairment in this disease occurs through a combination of the inhibition of specific enzymes and transporters, limitation in the availability of substrates for mitochondrial metabolic pathways and oxidative damage
Subject: Degeneração neural
DNA mitocondrial
Metabolismo energético
Country: Alemanha
Editor: Springer
Rights: Fechado
Identifier DOI: 10.1007/s10863-011-9330-2
Date Issue: 2011
Appears in Collections:FCM - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-79952317855.pdf303.98 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.