Mitochondrial dysfunction in Parkinson's disease

Mitochondrion. 2007 Feb-Apr;7(1-2):58-62. doi: 10.1016/j.mito.2006.12.002. Epub 2006 Dec 13.

Abstract

Parkinson's disease (PD) is one of the most common neurodegenerative disorders characterized by resting tremor, rigidity, and bradykinesia. The primary cause of PD is still unknown, but oxidative stress and mitochondrial dysfunction have been implicated as important contributors to neuronal death in substantia nigra (SN) of PD. Considering neurons as post-mitotic cells, neurons could have error-avoiding mechanism against oxidative DNA damage. Indeed, several DNA repairing enzymes such as MTH1, OGG1, and MUTYH express in human brain. All the three enzymes up-regulated in the SN of PD patients, suggesting these three enzymes cooperate in mitochondrial DNA repairing in PD brain.

Publication types

  • Review

MeSH terms

  • Animals
  • Antioxidants / physiology
  • DNA Glycosylases / genetics
  • DNA Repair Enzymes / genetics
  • DNA, Mitochondrial / genetics*
  • Humans
  • MPTP Poisoning / physiopathology
  • Mitochondria / pathology
  • Mitochondria / physiology*
  • Oxidative Stress / physiology
  • Parkinson Disease / genetics
  • Parkinson Disease / physiopathology*
  • Phosphoric Monoester Hydrolases / genetics

Substances

  • Antioxidants
  • DNA, Mitochondrial
  • Phosphoric Monoester Hydrolases
  • DNA Glycosylases
  • mutY adenine glycosylase
  • oxoguanine glycosylase 1, human
  • 8-oxodGTPase
  • DNA Repair Enzymes