Role of peroxidases in Parkinson disease : A hypothesis

被引:43
作者
Everse, J [1 ]
Coates, PW [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Lubbock, TX 79430 USA
关键词
peroxidase; Parkinson disease; cytotoxicity; myeloperoxidase; cytochrome c; free radicals;
D O I
10.1016/j.freeradbiomed.2005.01.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extensive research has been done to elucidate the underlying molecular events causing neurodegenerative diseases such as Parkinson disease, yet the cause and the individual steps in the progression of such diseases are still unknown. Here we advance the hypothesis that, rather than or in addition to inorganic radical molecules, heme-containing peroxidase enzymes may play a major role in the etiology of Parkinson disease. This hypothesis is based on the following considerations: (1) several heme-containing enzymes with peroxidase activity are present in the substantia nigra pars compacta; (2) these peroxidases have the ability to catalyze the oxidation of proteins and lipids; (3) certain heme peroxidases are known to destroy cells in vivo; (4) heme peroxidases have the stability and specificity that could account for the fact that specific molecules and cells are subject to damage in Parkinson disease, rather than a random destruction; (5) heme peroxidase activity could account for certain reactions in connection with parkinsonism that thus far have not been adequately explained; and (6) the participation of a heme peroxidase could explain some recent observations that are inconsistent with the oxyradical theory. The peroxidase-catalyzed oxidative pathway proposed here does not preclude the participation of apoptosis as an additional mechanism for cell destruction. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1296 / 1310
页数:15
相关论文
共 147 条
  • [41] EDELSON PJ, 1973, J EXP MED, V138, P318, DOI 10.1084/jem.138.1.318
  • [42] PROSTAGLANDIN-H SYNTHASE AND XENOBIOTIC OXIDATION
    ELING, TE
    THOMPSON, DC
    FOUREMAN, GL
    CURTIS, JF
    HUGHES, MF
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1990, 30 : 1 - 45
  • [43] EVERSE J, 1994, METHOD ENZYMOL, V231, P547
  • [44] The cytotoxic activity of lactoperoxidase: Enhancement and inhibition by neuroactive compounds
    Everse, J
    Coates, PW
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (06) : 839 - 849
  • [45] The toxicities of native and modified hemoglobins
    Everse, J
    Hsia, N
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (06) : 1075 - 1099
  • [46] EVERSE J, 1991, PEROXIDASES CHEM BIO, V1
  • [47] Everse J., 1991, PEROXIDASES CHEM BIO, V2
  • [48] ANTITUMOUR ACTIVITY OF PEROXIDASES
    EVERSE, KE
    LIN, H
    STUYT, EL
    BRADY, JC
    BUDDINGH, F
    EVERSE, J
    [J]. BRITISH JOURNAL OF CANCER, 1985, 51 (05) : 743 - 746
  • [49] Cyclooxygenase-2-deficient mice are resistant to 1-methyl-4-phenyl1,2,3,6-tetrahydropyridine-induced damage of dopaminergic neurons in the substantia nigra
    Feng, ZH
    Wang, TG
    Li, DD
    Fung, P
    Wilson, BC
    Liu, B
    Ali, SF
    Langenbach, R
    Hong, JS
    [J]. NEUROSCIENCE LETTERS, 2002, 329 (03) : 354 - 358
  • [50] Increased nitrotyrosine immunoreactivity in substantia nigra neurons in MPTP treated baboons is blocked by inhibition of neuronal nitric oxide synthase
    Ferrante, RJ
    Hantraye, P
    Brouillet, E
    Beal, MF
    [J]. BRAIN RESEARCH, 1999, 823 (1-2) : 177 - 182