Therapeutic role of coenzyme Q10 in Parkinson's disease

被引:55
作者
Shults, CW
机构
[1] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[2] VA San Diego Healthcare Syst, Serv Neurol, San Diego, CA USA
关键词
coenzyme Q(10); Parkinson's disease; mitochondria; neuroprotection; apoptosis;
D O I
10.1016/j.pharmthera.2005.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 Q(10), 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 Q(10) can affect certain of these processes. Levels of coenzyme Q(10) 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 Q(10) can protect the nigrostriatal dopaminergic system. A phase IIb trial or coenzyme Q(10) in patients with early, untreated PD demonstrated a positive trend for coenzyme Q(10) to slow progressive disability that occurs, in PD. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:120 / 130
页数:11
相关论文
共 108 条
[1]   INVOLVEMENT OF FREE-RADICALS IN MPP(+) NEUROTOXICITY AGAINST RAT DOPAMINERGIC-NEURONS IN CULTURE [J].
AKANEYA, Y ;
TAKAHASHI, M ;
HATANAKA, H .
NEUROSCIENCE LETTERS, 1995, 193 (01) :53-56
[2]  
Alam ZI, 1997, J NEUROCHEM, V69, P1326
[3]   Oxidative DNA damage in the parkinsonian brain: An apparent selective increase in 8-hydroxyguanine levels in substantia nigra [J].
Alam, ZI ;
Jenner, A ;
Daniel, SE ;
Lees, AJ ;
Cairns, N ;
Marsden, CD ;
Jenner, P ;
Halliwell, B .
JOURNAL OF NEUROCHEMISTRY, 1997, 69 (03) :1196-1203
[4]   Does neuronal loss in Parkinson's disease involve programmed cell death? [J].
Andersen, JK .
BIOESSAYS, 2001, 23 (07) :640-646
[5]   NO EVIDENCE FOR ALTERED MUSCLE MITOCHONDRIAL-FUNCTION IN PARKINSONS-DISEASE [J].
ANDERSON, JJ ;
BRAVI, D ;
FERRARI, R ;
DAVIS, TL ;
BARONTI, F ;
CHASE, TN ;
DAGANI, F .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1993, 56 (05) :477-480
[6]  
[Anonymous], 1991, Biomedical and clinical aspects of coenzyme Q
[7]   Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[8]  
BARROSO N, 1993, CLIN CHEM, V39, P667
[9]   COENZYME-Q CONTENT IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM DIFFERENT BRAIN-REGIONS IN THE AGING RAT [J].
BATTINO, M ;
GORINI, A ;
VILLA, RF ;
GENOVA, ML ;
BOVINA, C ;
SASSI, S ;
LITTARRU, GP ;
LENAZ, G .
MECHANISMS OF AGEING AND DEVELOPMENT, 1995, 78 (03) :173-187
[10]   Coenzyme Q10 attenuates the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced loss of striatal dopamine and dopaminergic axons in aged [J].
Beal, MF ;
Matthews, RT ;
Tieleman, A ;
Shults, CW .
BRAIN RESEARCH, 1998, 783 (01) :109-114