Glutathione cycle in stable chronic obstructive pulmonary disease

被引:29
作者
Biljak, Vanja Radisic [1 ]
Rumora, Lada [2 ]
Cepelak, Ivana [2 ]
Pancirov, Dolores [3 ]
Popovic-Grle, Sanja [4 ]
Soric, Jasna [2 ]
Grubisic, Tihana Zanic [2 ]
机构
[1] Univ Clin Diabet Endocrinol & Metab Dis Vuk Vrhov, Dept Lab Med, Zagreb 10000, Croatia
[2] Univ Zagreb, Dept Med Biochem & Haematol, Fac Pharm & Biochem, Zagreb 41000, Croatia
[3] Gen Hosp Dr Ivo Pedisic, Dept Pulmonol, Petrinja, Croatia
[4] Univ Hosp Lung Dis Jordanovac, Sch Med, Zagreb, Croatia
关键词
chronic obstructive pulmonary disease; glutathione peroxidase; glutathione reductase; oxidative stress; smoking; total glutathione; OXIDATIVE STRESS; ERYTHROCYTE GLUTATHIONE; LUNG; PEROXIDASE; ANTIOXIDANTS; PLATELETS; REDUCTASE; DEFENSE;
D O I
10.1002/cbf.1675
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation and oxidant/antioxidant imbalance. Glutathione is the most abundant cellular low-molecular weight thiol and the glutathione redox cycle is the fundamental component of the cellular antioxidant defence system. Concentration of total glutathione and catalytic activities of glutathione peroxidase and glutathione reductase were determined in peripheral blood of patients (n = 109) and healthy subjects (n = 51). Concentration of total glutathione in patients was not changed in comparison to healthy controls. However, we found statistically significant difference between patients with moderate and severe disease stages. Glutathione reductase activity was increased, while glutathione proxidase activity was decreased in the patients with COPD, when compared to healthy controls. We found no significant difference in glutathione peroxidase and glutathione reductase activities between stages. Patients who smoked had lower concentration of total glutathione compared with former smokers and never-smoking patients. Lung function parameters were inversely associated with glutathione level. Evidence is presented for differential modulation of glutathione peroxidase and glutathione reductase activities in peripheral blood of patients with stable COPD. We suppose that in addition to glutathione biosynthesis, glutathione reductase-dependent regulation of the glutathione redox state is vital for protection against oxidative stress. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:448 / 453
页数:6
相关论文
共 37 条
[1]
Hyperhomocysteinemia and changed plasma thiol redox status in chronic obstructive pulmonary disease [J].
Andersson, A ;
Ankerst, J ;
Lindgren, A ;
Larsson, K ;
Hultberg, B .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2001, 39 (03) :229-233
[2]
Arthur JR, 2000, CELL MOL LIFE SCI, V57, P1825
[3]
MICROTITER PLATE ASSAY FOR THE MEASUREMENT OF GLUTATHIONE AND GLUTATHIONE DISULFIDE IN LARGE NUMBERS OF BIOLOGICAL SAMPLES [J].
BAKER, MA ;
CERNIGLIA, GJ ;
ZAMAN, A .
ANALYTICAL BIOCHEMISTRY, 1990, 190 (02) :360-365
[4]
Bowler Russell P, 2004, COPD, V1, P255, DOI 10.1081/COPD-200027031
[5]
Glutathione peroxidases and redox-regulated transcription factors [J].
Brigelius-Flohe, Regina .
BIOLOGICAL CHEMISTRY, 2006, 387 (10-11) :1329-1335
[6]
Effects of organic and inorganic selenium supplementation on selenoenzyme activity in blood lymphoctyes, granulocytes, platelets and erythrocytes [J].
Brown, KM ;
Pickard, K ;
Nicol, F ;
Beckett, GJ ;
Duthie, GG ;
Arthur, JR .
CLINICAL SCIENCE, 2000, 98 (05) :593-599
[7]
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[8]
Glutathione in defense and signaling - Lessons from a small thiol [J].
Dickinson, DA ;
Forman, HJ .
CELL SIGNALING, TRANSCRIPTION, AND TRANSLATION AS THERAPEUTIC TARGETS, 2002, 973 :488-504
[9]
GIPP JJ, 2001, SOC TOX 40 ANN M, V60, P210
[10]
Yeast glutathione reductase is required for protection against oxidative stress and is a target gene for yAP-1 transcriptional regulation [J].
Grant, CM ;
Collinson, LP ;
Roe, JH ;
Dawes, IW .
MOLECULAR MICROBIOLOGY, 1996, 21 (01) :171-179