Biomarkers of oxidative stress in schizophrenic and control subjects

被引:59
作者
Young, J.
McKinney, S. B.
Ross, B. M.
Wahle, K. W. J.
Boyle, S. P.
机构
[1] Robert Gordon Univ, Sch Pharm, Aberdeen AB9 1FR, Scotland
[2] Dochfour Business Ctr, Ness Fdn, Inverness, Scotland
[3] NHS Highland, Inverness, Scotland
[4] Lakehead Univ, No Ontario Sch Med, Div Med Sci, Thunder Bay, ON P7B 5E1, Canada
[5] Robert Gordon Univ, Sch Life Sci, Aberdeen AB9 1FR, Scotland
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2007年 / 76卷 / 02期
关键词
D O I
10.1016/j.plefa.2006.11.003
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
Increasing evidence indicates that oxidative injury exists in schizophrenia. Although it may not be the main cause, oxidative damage has been suggested to contribute to the pathophysiology and may account for deteriorating course and poor outcome in schizophrenia. A human study was undertaken, therefore, to investigate possible differences in biomarkers of DNA, lipid and protein oxidation in schizophrenic (n = 16) and control subjects (n = 17). Plasma vitamin C levels were also compared in both groups. Cellular DNA damage and plasma protein carbonyl levels were increased in the schizophrenic group compared to control subjects but not significantly. However, DNA damage in lymphocytes from the male schizophrenic group was significantly higher than the female group. Biomarkers of lipid peroxidation and plasma vitamin C levels also revealed no significant difference between the two groups under investigation, although a significant elevation in plasma vitamin C was observed in the female control group when compared to the male groups. Crown Copyright (c) 2006 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:73 / 85
页数:13
相关论文
共 59 条
[1]   Supplementation with a combination of ω-3 fatty acids and antioxidants (vitamins E and C) improves the outcome of schizophrenia [J].
Arvindakshan, M ;
Ghate, M ;
Ranjekar, PK ;
Evans, DR ;
Mahadik, SP .
SCHIZOPHRENIA RESEARCH, 2003, 62 (03) :195-204
[2]  
AVRINDAKSHAN M, 2003, BIOL PSYCHIAT, V53, P56
[3]   Bioavailability and efficiency of rutin as an antioxidant: a human supplementation study [J].
Boyle, SP ;
Dobson, VL ;
Duthie, SJ ;
Hinselwood, DC ;
Kyle, JAM ;
Collins, AR .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2000, 54 (10) :774-782
[4]   Absorption and DNA protective effects of flavonoid glycosides from an onion meal [J].
Boyle, SP ;
Dobson, VL ;
Duthie, SJ ;
Kyle, JAM ;
Collins, AR .
EUROPEAN JOURNAL OF NUTRITION, 2000, 39 (05) :213-223
[5]   Protein carbonyl measurement by a sensitive ELISA method [J].
Buss, H ;
Chan, TP ;
Sluis, KB ;
Domigan, NM ;
Winterbourn, CC .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (03) :361-366
[6]   The association between schizophrenia and cancer: a population-based mortality study [J].
Cohen, ME ;
Dembling, B ;
Schorling, JB .
SCHIZOPHRENIA RESEARCH, 2002, 57 (2-3) :139-146
[7]   Supplementation of vitamin C with atypical antipsychotics reduces oxidative stress and improves the outcome of schizophrenia [J].
Dakhale, GN ;
Khanzode, SD ;
Khanzode, SS ;
Saoji, A .
PSYCHOPHARMACOLOGY, 2005, 182 (04) :494-498
[8]   4-hydroxynonenal and cell signalling [J].
Dianzani, MU .
FREE RADICAL RESEARCH, 1998, 28 (06) :553-560
[9]   Red cell membrane fatty acids, cytosolic phospholipase-A2 and schizophrenia [J].
Doris, AB ;
Wahle, K ;
MacDonald, A ;
Morris, S ;
Coffey, I ;
Muir, W ;
Blackwood, D .
SCHIZOPHRENIA RESEARCH, 1998, 31 (2-3) :185-196
[10]   Cryopreserved versus freshly isolated lymphocytes in human biomonitoring: endogenous and induced DNA damage, antioxidant status and repair capability [J].
Duthie, SJ ;
Pirie, L ;
Jenkinson, AM ;
Narayanan, S .
MUTAGENESIS, 2002, 17 (03) :211-214