Plasma glutathione peroxidase (GSH-Px) concentration is elevated in rheumatoid arthritis: a case–control study

被引:10
作者
Glenn A. Jacobson
Stephen J. Ives
Christian Narkowicz
Graeme Jones
机构
[1] University of Tasmania,School of Pharmacy
[2] University of Tasmania,Menzies Research Institute Tasmania
来源
Clinical Rheumatology | 2012年 / 31卷
关键词
Glutathione peroxidase; Oxidative stress; Plasma; Rheumatoid arthritis;
D O I
暂无
中图分类号
学科分类号
摘要
Plasma glutathione peroxidase (GSH-Px) by enzyme-linked immunosorbent assay (ELISA) offers a complimentary measurement approach to traditional GSH-Px activity methods. The aim was to investigate whether GSH-Px measured by ELISA in rheumatoid arthritis patients was elevated compared to controls. This was a case–control study with rheumatoid arthritis patients recruited from private practice and gender and age-matched controls randomly selected from the electoral role. GSH-Px concentration was measured by ELISA. Plasma malondialdehyde was used as a measure of oxidative stress, and antioxidant capacity was measured based on reduction of Cu++ to Cu+ by antioxidants in the sample. Disease severity was measured using the Health Assessment Questionnaire-Disability Index (HAQ-DI) and C-reactive protein was measured using an immunoturbidometric method. A total of 74 patients were recruited, consisting of 35 rheumatoid arthritis cases and 39 healthy controls. There were no differences between rheumatoid arthritis cases and controls for oxidative stress and antioxidant capacity; however, GSH-Px concentration was markedly elevated in the rheumatoid arthritis sufferers (85.9 ± 147.7 versus 17.3 ± 13.0 mg/L, respectively; mean ± SD; p < 0.01). GSH-Px levels were not associated with severity measured by the HAQ-DI or C-reactive protein. Patients with rheumatoid arthritis demonstrated increased GSH-Px consistent with an adaptive upregulation of GSH-Px to protect against oxidative stress.
引用
收藏
页码:1543 / 1547
页数:4
相关论文
共 118 条
[1]
Rahman I(2006)Oxidant and antioxidant balance in the airways and airway diseases Eur J Pharmacol 533 222-239
[2]
Biswas SK(1987)Comparative study of the enzymatic defense systems against oxygen-derived free radicals: the key role of glutathione peroxidase Free Radic Biol Med 3 3-7
[3]
Kode A(1987)Characterization of the major hydroperoxide-reducing activity of human plasma. Purification and properties of a selenium-dependent glutathione peroxidase J Biol Chem 262 17398-17403
[4]
Raes M(1987)Purification and characterization of human plasma glutathione peroxidase: a selenoglycoprotein distinct from the known cellular enzyme Arch Biochem Biophys 256 677-686
[5]
Michiels C(2003)Quantitative speciation of selenium in human serum by affinity chromatography coupled to post-column isotope dilution analysis ICP-MS J Anal At Spectrom 18 1210-1216
[6]
Remacle J(1993)Determination of the distribution of selenium between glutathione peroxidase, selenoprotein P, and albumin in plasma Anal Biochem 208 176-181
[7]
Maddipati KR(2001)Selenium, selenoproteins and human health: a review Public Health Nutr 4 593-599
[8]
Marnett LJ(2003)The role of reactive oxygen species in homeostasis and degradation of cartilage Osteoarthr Cartil 11 747-755
[9]
Takahashi K(2002)Nitric oxide-mediated chondrocyte cell death requires the generation of additional reactive oxygen species Arthritis Rheum 46 394-403
[10]
Avissar N(1999)Aggrecan degradation in chondrocytes is mediated by reactive oxygen species and protected by antioxidants Free Radic Res 30 395-405