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doi:10.1016/j.pharmthera.2005.02.002    
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Copyright © 2005 Elsevier Inc. All rights reserved.

Associate editor: M.M. Mouradian

Therapeutic role of coenzyme Q10 in Parkinson's disease

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Clifford W. ShultsCorresponding Author Contact Information, E-mail The Corresponding Author

Department of Neurosciences, University of California, San Diego, La Jolla, CA, United States

Neurology Service, VA San Diego Healthcare System, San Diego, CA, United States


Available online 21 April 2005.

Abstract

Mitochondrial dysfunction has been well established to occur in Parkinson's disease (PD) and appears to play a role in the pathogenesis of the disorder. A key component of the mitochondrial electron transport chain (ETC) is coenzyme Q10, which not only serves as the electron acceptor for complexes I and II of the ETC but is also an antioxidant. In addition to being crucial to the bioenergetics of the cell, mitochondria play a central role in apoptotic cell death through a number of mechanisms, and coenzyme Q10 can affect certain of these processes. Levels of coenzyme Q10 have been reported to be decreased in blood and platelet mitochondria from PD patients. A number of preclinical studies in in vitro and in vivo models of PD have demonstrated that coenzyme Q10 can protect the nigrostriatal dopaminergic system. A phase II trial of coenzyme Q10 in patients with early, untreated PD demonstrated a positive trend for coenzyme Q10 to slow progressive disability that occurs in PD.

Keywords: Coenzyme Q10; Parkinson's disease; Mitochondria; Neuroprotection; Apoptosis

Abbreviations: AIF, apoptosis-inducing factor; ATP, adenosine 5′ triphosphate; C. elegans, Caenorhabditis elegans; CoA, coenzyme A; ETC, electron transport chain; FADH2, flavin adenine dinucleotide; IAP, inhibitors of apoptosis proteins; MOMP, mitochondrial outer membrane permeabilization; MPP+, 1-methyl-4-phenylpyridinium; MPTP, 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine; NADH, nicotinamide adenine dinucleotide; PD, Parkinson's disease; PTP, permeability transition pore; ROS, reactive oxygen species; SOD2, superoxide dismutase 2 or manganese superoxide dismutase; ΔΨm, transmembrane potential; TH-IR, tyrosine hydroxylase immunoreactive; UCP, uncoupling proteins; UPDRS, Unified Parkinson Disease Rating Scale

Article Outline

1. Introduction
2. Mitochondria and bioenergetics and oxidative stress
3. Mitochondria and apoptosis
4. Coenzyme Q10 and Parkinson's disease
5. Preclinical studies of coenzyme Q10 in models of Parkinson's disease
6. Effects of coenzyme Q10 on life span
7. Trials of coenzyme Q10 in Parkinson's disease patients
7.1. Trials in Parkinson's disease patients on medication for Parkinson's disease
7.2. Trials in Parkinson's disease patients with early disease not requiring medication
7.3. Ongoing trials
7.4. Future trials
8. Conclusion
Acknowledgements
References


Corresponding Author Contact InformationDepartment of Neurosciences-0662, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, United States. Tel.: 858 642 3685; fax: 858 552 7513.

 
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