| Literature DB >> 23602907 |
Abstract
Huntington's disease (HD) is a neurodegenerative disorder with an autosomal dominant expression pattern and typically a late-onset appearance. HD is a movement disorder with a heterogeneous phenotype characterized by involuntary dance-like gait, bioenergetic deficits, motor impairment, and cognitive and psychiatric deficits. Compelling evidence suggests that increased oxidative stress and mitochondrial dysfunction may underlie HD pathogenesis. However, the exact mechanisms underlying mutant huntingtin-induced neurological toxicity remain unclear. The objective of this paper is to review recent literature regarding the role of oxidative DNA damage in mitochondrial dysfunction and HD pathogenesis.Entities:
Keywords: 3-NPA; 3-nitropropionic acid; 7,8-dihydro-8-oxoguanine-DNA glycosylase; 8-OHdG; 8-hydroxydeoxyguanosine; AP; ARE; ATM; ATR; BER; DNA repair; FEN1; HD; Huntington’s disease; MMR; Mitochondrial DNA; Mitochondrial bioenergetics; Mitochondrial dysfunction; NF-E2-related factor 2; Nrf2; OGG1; Oxidative stress; PGC-1α; POL β; PPARγ; ROS; Rad3-related kinase; Sirt; antioxidant response element; apurinic/apyrimidinic; ataxia telangiectasia mutated kinase; base excision repair; flap endonuclease 1; mismatch repair; peroxisome proliferator-activated receptor-γ; peroxisome proliferator-activated receptor-γ coactivator-1 α; polymerase beta; reactive oxygen species; sirtuins
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Year: 2013 PMID: 23602907 PMCID: PMC3722255 DOI: 10.1016/j.freeradbiomed.2013.04.017
Source DB: PubMed Journal: Free Radic Biol Med ISSN: 0891-5849 Impact factor: 7.376