Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Sep 2:2018:9163040.
doi: 10.1155/2018/9163040. eCollection 2018.

The Sources of Reactive Oxygen Species and Its Possible Role in the Pathogenesis of Parkinson's Disease

Affiliations
Review

The Sources of Reactive Oxygen Species and Its Possible Role in the Pathogenesis of Parkinson's Disease

Minrui Weng et al. Parkinsons Dis. .

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder characterized by progressive loss of dopaminergic neurons in the substantia nigra. The precise mechanism underlying pathogenesis of PD is not fully understood, but it has been widely accepted that excessive reactive oxygen species (ROS) are the key mediator of PD pathogenesis. The causative factors of PD such as gene mutation, neuroinflammation, and iron accumulation all could induce ROS generation, and the later would mediate the dopaminergic neuron death by causing oxidation protein, lipids, and other macromolecules in the cells. Obviously, it is of mechanistic and therapeutic significance to understand where ROS are derived and how ROS induce dopaminergic neuron damage. In the present review, we try to summarize and discuss the main source of ROS in PD and the key pathways through which ROS mediate DA neuron death.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Schematic pathway of ROS generation and induction of DA neurons death. Mitochondria dysfunction, dopamine, neuroinflammation, iron, and genetic mutations solely or synergistically induce ROS generation, which could induce dopaminergic neurons death via protein, lipid, and DNA oxidation.

Similar articles

Cited by

References

    1. Jellinger K. Neuropathological substrates of Alzheimers disease and Parkinsons disease. Journal of Neural Transmission. 1987;24:109–129. - PubMed
    1. Moon H. E., Paek S. H. Mitochondrial dysfunction in Parkinson’s disease. Experimental Neurobiology. 2015;24:103–116. doi: 10.5607/en.2015.24.2.103. - DOI - PMC - PubMed
    1. Whitworth A. J., Pallanck L. J. Genetic models of Parkinson’s disease: mechanisms and therapies. SEB Experimental Biology Series. 2008;60:93–113. - PubMed
    1. Shadrina M. I., Slominsky P. A. Molecular genetics of Parkinson’s disease. Russian Journal of Genetics. 2006;42(8):858–871. doi: 10.1134/s1022795406080035. - DOI - PubMed
    1. Chou A. P., Maidment N., Klintenberg R., et al. Ziram causes dopaminergic cell damage by inhibiting e1 ligase of the proteasome. Journal of Biological Chemistry. 2008;283(50):34696–34703. doi: 10.1074/jbc.m802210200. - DOI - PMC - PubMed

LinkOut - more resources