The chemical process of oxidative stress by copper(II) and iron(III) ions in several neurodegenerative disorders

被引:35
作者
Nishida, Yuzo [1 ]
机构
[1] Kanazawa Med Univ, Med Res Inst, Kahoku, Ishikawa 9200263, Japan
来源
MONATSHEFTE FUR CHEMIE | 2011年 / 142卷 / 04期
关键词
ALS; SOD; Hydrogen peroxide; NTBI; Binuclear iron(III) species; AMYOTROPHIC-LATERAL-SCLEROSIS; CU; ZN-SUPEROXIDE DISMUTASE MUTANT; RAPID DISEASE PROGRESSION; GAIN-OF-FUNCTION; PRION PROTEIN; HYDROGEN-PEROXIDE; FERRIC NITRILOTRIACETATE; SUPEROXIDE-DISMUTASE; LIPID-PEROXIDATION; CELLULAR-RESPONSE;
D O I
10.1007/s00706-010-0444-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The variety of factors and events involved in neurodegeneration renders the subject a major challenge. Neurodegenerative disorders include a number of different pathological conditions, which share similar critical metabolic processes, such as protein aggregation and oxidative stress, both of which are associated with the involvement of transition metal ions. In this review, amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD), and prion disease are discussed, with the aim of identifying the common trends underlying these devastating neurological conditions by elucidating the chemical process of the oxidative stress due to copper(II) and iron(III) ions.
引用
收藏
页码:375 / 384
页数:10
相关论文
共 78 条
  • [1] Abe K, 2008, Z NATURFORSCH C, V63, P151
  • [2] Alam ZI, 1997, J NEUROCHEM, V69, P1326
  • [3] [Anonymous], 1982, JPN ARCH INTERN MED
  • [4] Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin
    Babcock, M
    deSilva, D
    Oaks, R
    DavisKaplan, S
    Jiralerspong, S
    Montermini, L
    Pandolfo, M
    Kaplan, J
    [J]. SCIENCE, 1997, 276 (5319) : 1709 - 1712
  • [5] SUPEROXIDE-DISMUTASE-1 WITH MUTATIONS LINKED TO FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS POSSESSES SIGNIFICANT ACTIVITY
    BORCHELT, DR
    LEE, MK
    SLUNT, HS
    GUARNIERI, M
    XU, ZS
    WONG, PC
    BROWN, RH
    PRICE, DL
    SISODIA, SS
    CLEVELAND, DW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) : 8292 - 8296
  • [6] Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia
    Bradley, JL
    Blake, JC
    Chamberlain, S
    Thomas, PK
    Cooper, JM
    Schapira, AHV
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (02) : 275 - 282
  • [7] AMYOTROPHIC-LATERAL-SCLEROSIS - RECENT INSIGHTS FROM GENETICS AND TRANSGENIC MICE
    BROWN, RH
    [J]. CELL, 1995, 80 (05) : 687 - 692
  • [8] Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1
    Bruijn, LI
    Houseweart, MK
    Kato, S
    Anderson, KL
    Anderson, SD
    Ohama, E
    Reaume, AG
    Scott, RW
    Cleveland, DW
    [J]. SCIENCE, 1998, 281 (5384) : 1851 - 1854
  • [9] Brain protein oxidation in age-related neurodegenerative disorders that are associated with aggregated proteins
    Butterfield, DA
    Kanski, J
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (09) : 945 - 962
  • [10] Interactions between prion protein isoforms: the kiss of death?
    Caughey, B
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (04) : 235 - 242