Oxidative stress and status of antioxidant enzymes in children with Kashin-Beck disease

被引:44
作者
Wang, W. [1 ]
Wei, S. [2 ]
Luo, M. [1 ]
Yu, B. [1 ]
Cao, J. [1 ]
Yang, Z. [1 ]
Wang, Z. [1 ]
Goldring, M. B. [3 ,4 ]
Chen, J. [1 ]
机构
[1] Xi An Jiao Tong Univ, Minist Educ, Coll Med, Key Lab Environm & Genes Related Dis,Inst Endem D, Xian 710061, Shaanxi, Peoples R China
[2] Yanan Univ, Affiliated Hosp, Yanan 716000, Shaanxi, Peoples R China
[3] Weill Cornell Med Coll, Hosp Special Surg, Div Res, New York, NY 10021 USA
[4] Weill Cornell Med Coll, Dept Cell & Dev Biol, New York, NY 10021 USA
基金
中国国家自然科学基金;
关键词
Kashin-Beck disease; Oxidative stress; Antioxidant enzyme; Cartilage; EXTRACELLULAR-SUPEROXIDE DISMUTASE; HUMAN OSTEOARTHRITIC CARTILAGE; NORMAL HUMAN CHONDROCYTES; RHEUMATOID-ARTHRITIS; ARTICULAR-CARTILAGE; LIPID-PEROXIDATION; OXIDANT DAMAGE; EXPRESSION; DEGRADATION; OXYGEN;
D O I
10.1016/j.joca.2013.08.002
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objectives: To clarify whether there is oxidative stress in Kashin-Beck disease (KBD) and if cartilage damage from reactive oxygen species (ROS) and oxidative stress mediate the chondral necrosis in articular cartilage of KBD. Methods: We recruited 64 KBD patients, 46 healthy children from severely affected KBD regions, 81 healthy children from a non-severely affected KBD endemic regions, and 91 healthy control children from a non-KBD region. Ten patients with KBD from the non-severely affected KBD regions were included in the experiment. The 2,3-DAN fluorescence technique was used to test selenium in the hair and blood. The biochemical techniques used to test the indicators of oxidative stress included thiobarbituric acid reactive substances (TBARS) levels, and antioxidant enzyme activities in serum samples. Histochemical staining was used to detect proteoglycans in cartilage sections. The 4-hydroxy-2-nonenal (4-HNE) and 8-hydroxydeoxyguanisine (8-0HdG) were localized by immunohistochemistry. Results: The levels of TSARS in serum were significantly increased in KBD children. The levels of antioxidants in serum were significantly higher in both KBD and normal children from KBD regions than in the normal children from non-KBD regions. The percentage of chondrocytes staining for 4-HNE and 8-OHdG in KBD patients was significantly higher than in controls. Staining for 4-HNE and 8-0HdG in KBD patients was prominent in all zones of articular cartilage, especially in the necrotic chondrocytes of the deep zone. Conclusion: KBD is an oxidative stress-related disease, and the oxidative stress in cartilage contributes to the pathology of cartilage damage in KBD. (C) 2013 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1781 / 1789
页数:9
相关论文
共 44 条
[1]   Large-scale gene expression profiling reveals major pathogenetic pathways of cartilage degeneration in osteoarthritis [J].
Aigner, Thomas ;
Fundel, Katrin ;
Saas, Joachim ;
Gebhard, Pia M. ;
Haag, Jochen ;
Weiss, Tilo ;
Zien, Alexander ;
Obermayr, Franz ;
Zimmer, Ralf ;
Bartnik, Eckart .
ARTHRITIS AND RHEUMATISM, 2006, 54 (11) :3533-3544
[2]  
ALLANDER E, 1994, SCAND J RHEUMATOL, P1
[3]   The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay [J].
Benzie, IFF ;
Strain, JJ .
ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) :70-76
[4]   Oxidative damage in synovial tissue is associated with in vivo hypoxic status in the arthritic joint [J].
Biniecka, Monika ;
Kennedy, Aisling ;
Fearon, Ursula ;
Ng, Chin Teck ;
Veale, Douglas J. ;
O'Sullivan, Jacintha N. .
ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (06) :1172-1178
[5]   OXYGEN RADICALS AS EFFECTORS OF CARTILAGE DESTRUCTION - DIRECT DEGRADATIVE EFFECT ON MATRIX COMPONENTS AND INDIRECT ACTION VIA ACTIVATION OF LATENT COLLAGENASE FROM POLYMORPHONUCLEAR LEUKOCYTES [J].
BURKHARDT, H ;
SCHWINGEL, M ;
MENNINGER, H ;
MACARTNEY, HW ;
TSCHESCHE, H .
ARTHRITIS AND RHEUMATISM, 1986, 29 (03) :379-387
[6]   Articular cartilage metabolism in patients with Kashin-Beck Disease: an endemic osteoarthropathy in China [J].
Cao, J. ;
Li, S. ;
Shi, Z. ;
Yue, Y. ;
Sun, J. ;
Chen, J. ;
Fu, Q. ;
Hughes, C. E. ;
Caterson, B. .
OSTEOARTHRITIS AND CARTILAGE, 2008, 16 (06) :680-688
[7]   Oxidant damage in Kashin-Beck disease and a rat Kashin-Beck disease model by employing T-2 toxin treatment under selenium deficient conditions [J].
Chen, Jing-hong ;
Xue, Senghai ;
Li, Siyuan ;
Wang, Zhi-lun ;
Yang, Haojie ;
Wang, Wei ;
Song, Daiqing ;
Zhou, Xiaorong ;
Chen, Chen .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2012, 30 (08) :1229-1237
[8]   Mitochondrial dysfunction activates cyclooxygenase 2 expression in cultured normal human chondrocytes [J].
Cillero-Pastor, Berta ;
Carames, Beatriz ;
Lires-Dean, Marcos ;
Vaamonde-Garcia, Carlos ;
Blanco, Francisco J. ;
Lopez-Armada, Maria J. .
ARTHRITIS AND RHEUMATISM, 2008, 58 (08) :2409-2419
[9]   Comparative Analysis of Gene Expression Profiles Between Primary Knee Osteoarthritis and an Osteoarthritis Endemic to Northwestern China, Kashin-Beck Disease [J].
Duan, Chen ;
Guo, Xiong ;
Zhang, Xiao-Dong ;
Yu, Han-Jie ;
Yan, Hua ;
Gao, Ying ;
Ma, Wei-Juan ;
Gao, Zong-Qiang ;
Xu, Peng ;
Lammi, Mikko .
ARTHRITIS AND RHEUMATISM, 2010, 62 (03) :771-780
[10]  
Feldmann M, 2001, CURR DIRECT AUTOIMMU, V3, P188