Evaluation of oxidative stress markers and intra-extracellular antioxidant activities in patients with endometriosis

被引:35
作者
Turkyilmaz, Esengul [1 ]
Yildirim, Melahat [1 ]
Cendek, Busra Demir [2 ]
Baran, Pervin [3 ]
Alisik, Murat [3 ]
Dalgaci, Ferit [1 ]
Yavuz, Ayse Filiz [4 ]
机构
[1] Ataturk Training & Res Hosp, Dept Gynecol & Obstet, Ankara, Turkey
[2] Sincan Nafiz Korez State Hosp, Dept Gynecol & Obstet, Ankara, Turkey
[3] Ataturk Training & Res Hosp, Dept Biochem, Ankara, Turkey
[4] Yildirim Beyazit Univ, Dept Gynecol & Obstet, Ankara, Turkey
关键词
Endometriosis; Total thiol; Native thiol; Catalase; CERULOPLASMIN; CA-125; WOMEN;
D O I
10.1016/j.ejogrb.2016.02.027
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: The aim of the study is to evaluate alterations in intracellular and extracellular antioxidant enzymes activities and serum oxidative stress markers in patients with endometriosis. Study design: The current prospective study consisted of 31 female patients with endometriosis and 27 healthy controls. Serum total thiol, native thiol, disulphide, catalase, myeloperoxidase, and ceruloplasmin concentrations were measured. Laboratory and clinical data of all participants were recorded to compare the differences between the study and the control groups. Results: Serum native thiol and total thiol levels in the study group were significantly lower than those in the control group [(p = 0.009, p = 0.03, respectively)]. Serum catalase levels are significantly higher in patients with endometriosis comparing to the control group (p = 0.009). Conclusions: The finding that significant differences in serum total thiol, native thiol, and catalase levels observed in endometriotic patients supports that oxidative stress carries weigh in the pathophysiological aspects of endometriosis. Also significantly low levels of extracellular antioxidants and significantly high levels of intracellular antioxidants in endometriotic patients may arise from differences of free radicals in endometriosis and the activity levels of endometriosis. These non-invasive serum markers might give us an opportunity to monitor the disease's progress during the treatment. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:164 / 168
页数:5
相关论文
共 33 条
[1]   Role of oxidative stress in female reproduction [J].
Agarwal, A ;
Gupta, S ;
Sharma, RK .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2005, 3 (1)
[2]   Direct evidence of caeruloplasmin antioxidant properties [J].
Atanasiu, RL ;
Stea, D ;
Mateescu, MA ;
Vergely, C ;
Dalloz, F ;
Briot, F ;
Maupoil, V ;
Nadeau, R ;
Rochette, L .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 189 (1-2) :127-135
[3]   Pathogenesis of endometriosis: the role of genetics, inflammation and oxidative stress [J].
Augoulea, A. ;
Alexandrou, A. ;
Creatsa, M. ;
Vrachnis, N. ;
Lambrinoudaki, I. .
ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2012, 286 (01) :99-103
[4]   Redox modifications of protein-thiols: Emerging roles in cell signaling [J].
Biswas, S ;
Chida, AS ;
Rahman, I .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (05) :551-564
[5]   MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER [J].
BRADLEY, PP ;
PRIEBAT, DA ;
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) :206-209
[6]  
Cai Zhiyou, 2013, J Biochem Pharmacol Res, V1, P15
[7]  
Canis M, 1997, FERTIL STERIL, V67, P817
[8]   Reactive oxygen species, cellular redox systems, and apoptosis [J].
Circu, Magdalena L. ;
Aw, Tak Yee .
FREE RADICAL BIOLOGY AND MEDICINE, 2010, 48 (06) :749-762
[9]   Oxidant Sensing by Reversible Disulfide Bond Formation [J].
Cremers, Claudia M. ;
Jakob, Ursula .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (37) :26489-26496
[10]  
Erel O, 1998, CLIN CHEM, V44, P2313