Time-dependent course of hyperbaric oxygen-induced oxidative effects in rat lung and erythrocytes

被引:25
作者
Ay, Hakan
Topal, Turgut
Uysal, Bulent
Ozler, Mehmet
Oter, Sukru [1 ]
Korkmaz, Ahmet
Dundar, Kadir
机构
[1] Gulhane Askeri Tip Akad, Dept Undersea & Hyperbar Med, TR-06018 Ankara, Turkey
[2] Gulhane Askeri Tip Akad, Dept Physiol, Ankara, Turkey
来源
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY | 2007年 / 34卷 / 08期
关键词
anti-oxidant enzymes; erythrocyte; hyperbaric oxygen; lung; oxidative stress;
D O I
10.1111/j.1440-1681.2007.04645.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The oxygen toxicity of hyperbaric oxygen (HBO) treatment has long been of interest. There is an extensive amount of information regarding the role oxidative stress plays after HBO exposure in different tissues, but the question of the persistence of this oxidative effect has not been thoroughly elucidated. 2. The present study was performed to elucidate the persistence of the oxidative effects of HBO on rat lungs and erythrocytes after they had been subjected to 100% oxygen exposure. 3. Rats were divided into five groups. All animals, except those in the control group, were subjected to 100% oxygen for 2 h at 3 ATA (equivalent to 300 kPa). Rats were killed at 30, 60, 90 or 120 min after exposure and thiobarbituric acid-reactive substances (TBARS) levels and the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were determined. 4. Thiobarbituric acid-reactive substances levels and SOD and GPx levels were found to be significantly increased in lung tissue up to 60 min after exposure. Superoxide dismutase activity persisted at significantly high values for 90 min after exposure in erythrocytes and the lung. The TBARS levels in erythrocytes were also significantly higher for 60 min, whereas increased GPx activity was observed to persist for only 30 min. 5. The oxidative effect of HBO exposure declines to physiological levels within 90 min at most for erythrocytes and in lung tissue in rats. Further studies should focus on the molecular mechanisms that can be activated during this time interval.
引用
收藏
页码:787 / 791
页数:5
相关论文
共 34 条
[1]   Influence of vitamin C and E supplementation on oxidative stress induced by hyperbaric oxygen in healthy men [J].
Bader, Nicolle ;
Bosy-Westphal, Anja ;
Koch, Andreas ;
Mueller, Manfred J. .
ANNALS OF NUTRITION AND METABOLISM, 2006, 50 (03) :173-176
[2]   Oxidative stress and antioxidant status in patients undergoing prolonged exposure to hyperbaric oxygen [J].
Benedetti, S ;
Lamorgese, A ;
Piersantelli, M ;
Pagliarani, S ;
Benvenuti, F ;
Canestrari, F .
CLINICAL BIOCHEMISTRY, 2004, 37 (04) :312-317
[3]  
BOADI WY, 1991, VET HUM TOXICOL, V33, P105
[4]  
Bocci VA, 2006, ARCH MED RES, V37, P425, DOI 10.1016/j.arcmed.2005.08.006
[5]  
Bonomo SR, 1998, UNDERSEA HYPERBAR M, V25, P211
[6]   Regional lipid peroxidation and protein oxidation in rat brain after hyperbaric oxygen exposure [J].
Chavko, M ;
Harabin, AL .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (07) :973-978
[7]   Antioxidant status in humans after exposure to hyperbaric oxygen [J].
Dennog, C ;
Radermacher, P ;
Barnett, YA ;
Speit, G .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 428 (1-2) :83-89
[8]   Protective effects of exogenously administered or endogenously produced melatonin on hyperbaric oxygen-induced oxidative stress in the rat brain [J].
Dundar, K ;
Topal, T ;
Ay, H ;
Oter, S ;
Korkmaz, A .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2005, 32 (11) :926-930
[9]   The effects of hyperbaric oxygen treatment on oxidative stress and SCE frequencies in humans [J].
Eken, A ;
Aydin, A ;
Sayal, A ;
Üstündag, A ;
Duydu, Y ;
Dündar, K .
CLINICAL BIOCHEMISTRY, 2005, 38 (12) :1133-1137
[10]  
FELDMEIER JJ, 2003, HYPERBARIC OXYGEN IN