Remarkable increase in the concentration of 8-hydroxyguanosine in cerebrospinal fluid from patients with Alzheimer's disease

被引:107
作者
Abe, T [1 ]
Tohgi, H [1 ]
Isobe, C [1 ]
Murata, T [1 ]
Sato, C [1 ]
机构
[1] Iwate Med Univ, Dept Neurol, Morioka, Iwate 0208505, Japan
关键词
Alzheimer's disease; 8-hydroxyguanosine; RNA; oxidative stress; cerebrospinal fluid;
D O I
10.1002/jnr.10349
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
To investigate the possible role of oxidative RNA damage in the pathogenesis of Alzheimer's disease (AD), the concentrations of the oxidative stress marker 8-hydroxyguanosine (8-OHG) were measured in the cerebrospinal fluid (CSF) and the serum of patients with AD and control subjects. The concentration of 8-OHG in CSF in AD patients was approximately fivefold that in controls (P < 0.001). The concentration of 8-OHG in CSF decreased significantly with the duration of illness (r(S) = -0.48, P < 0.05) and the progression of cognitive dysfunctions (r(S) = 0.67, P < 0.01). However, the concentration of 8-OHG in CSF showed no correlation with that in serum in both the controls and AD patients. In addition, the concentration of 8-OHG in serum was not significantly altered in AD patients compared to that in controls, suggesting that the 8-OHG concentrations in the CSF do not reflect those in serum and may be probably reflect those in brain tissue. These in vivo findings suggest a possible role of 8-OHG and increased oxidative RNA damage in the early stage of the development of AD. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:447 / 450
页数:4
相关论文
共 32 条
[1]
Amyloid β-peptide stimulates nitric oxide production in astrocytes through an NFκB-dependent mechanism [J].
Akama, KT ;
Albanese, C ;
Pestell, RG ;
Van Eldik, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (10) :5795-5800
[2]
*AM PSYCH ASS, 1994, DIAGN STAT MAN MENT, P133
[3]
AGING, ENERGY, AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISEASES [J].
BEAL, MF .
ANNALS OF NEUROLOGY, 1995, 38 (03) :357-366
[4]
HYDROGEN-PEROXIDE MEDIATES AMYLOID-BETA PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, JB ;
LESLEY, R ;
SCHUBERT, D .
CELL, 1994, 77 (06) :817-827
[5]
INCREASED NUMBER OF NADPH-D-POSITIVE NEURONS WITHIN THE SUBSTANTIA INNOMINATA IN ALZHEIMERS-DISEASE [J].
BENZING, WC ;
MUFSON, EJ .
BRAIN RESEARCH, 1995, 670 (02) :351-355
[6]
Oxidative stress and Alzheimer disease [J].
Christen, Y .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2000, 71 (02) :621S-629S
[7]
PRODUCTION OF SUPEROXIDE ANIONS BY A CNS MACROPHAGE, THE MICROGLIA [J].
COLTON, CA ;
GILBERT, DL .
FEBS LETTERS, 1987, 223 (02) :284-288
[8]
Dani SU, 1997, PRINCIPLES OF NEURAL AGING, P83
[9]
FIALA ES, 1989, CANCER RES, V49, P5518
[10]
Antioxidants, oxidative stress, and degenerative neurological disorders [J].
Floyd, RA .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 222 (03) :236-245