Influences of different stress models on the antioxidant status and lipid peroxidation in rat erythrocytes

被引:57
作者
Gümüslü, S [1 ]
Sarikçioglu, SB
Sahin, E
Yargiçoglu, P
Agar, A
机构
[1] Akdeniz Univ, Fac Med, Dept Biochem, TR-07070 Arapsuyu, Antalya, Turkey
[2] Akdeniz Univ, Fac Med, Dept Biophys, TR-07070 Arapsuyu, Antalya, Turkey
[3] Akdeniz Univ, Fac Med, Dept Physiol, TR-07070 Arapsuyu, Antalya, Turkey
关键词
cold stress; immobilization stress; cold plus immobilization stress; antioxidant enzymes; lipid peroxidation; erythrocyte; rat;
D O I
10.1080/1071576021000016508
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to investigate the influences of different stress models on the antioxidant status and lipid peroxidation (LPO) in erythrocytes of rats. Swiss-Albino female rats (3 months old) were used in this study. Rats were randomly divided into the following four groups; control group (C), cold stress group (CS), immobilization stress group (IS) and cold+immobilization stress group (CS+IS). Control group was kept in an animal laboratory (22+/-2degreesC). Rats in CS group were placed in cold room (5degreesC) for 15 min/day for 15 days. Rats in IS group were immobilized for 180 min/day for 15 days. Rats in CS+IS group were exposed to both cold and immobilization stresses for 15 days. At the end of experimental periods, the activities of glucose-6-phosphate dehydrogenase (G-6-PD), Cu,Zn-superoxide dismutase (Cu,Zn-SOD), catalase (CAT) and glutathione peroxidase (GSH-Px), and concentration of reduced glutathione (GSH) were measured. LPO was determined by measuring the contents of thiobarbituric acid-reactive substances (TBARS). Cu,Zn-SOD activity and TBARS concentration were increased after cold and immobilization stresses, but CAT and GSH-Px activities and GSH levels were decreased. Immobilization stress decreased the activity of G-6-PD. The activities of G-6-PD, CAT and GSH-Px, and the level of GSH were lower in CS+IS group than in the control group. Cu,Zn-SOD activity and TBARS levels were increased in CS+IS group when compared with the control group. From these findings, three stress models are thought to cause oxidative stress.
引用
收藏
页码:1277 / 1282
页数:6
相关论文
共 35 条
[1]  
AEBI HE, 1987, METHOD ENZYMAT AN, P273
[2]  
Andersen HR, 1997, CLIN CHEM, V43, P562
[3]  
[Anonymous], 1999, SAO PAULO MED J
[4]   Acute and chronic stress-induced oxidative gastrointestinal mucosal injury in rats and protection by bismuth subsalicylate [J].
Bagchi, D ;
Carryl, OR ;
Tran, MX ;
Bagchi, M ;
Garg, A ;
Milnes, MM ;
Williams, CB ;
Balmoori, J ;
Bagchi, DJ ;
Mitra, S ;
Stohs, SJ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1999, 196 (1-2) :109-116
[5]  
BARABOI VA, 1989, FIZIOL ZH SSSR, V35, P85
[6]  
Bian J S, 1997, Sheng Li Xue Bao, V49, P526
[7]   Antioxidant capacity of G-6-PD-deficient erythrocytes [J].
Bilmen, S ;
Aksu, TA ;
Gümüslü, S ;
Korgun, DK ;
Canatan, D .
CLINICA CHIMICA ACTA, 2001, 303 (1-2) :83-86
[8]  
Bondarenko T I, 1999, Ross Fiziol Zh Im I M Sechenova, V85, P1080
[9]   EFFECT OF COLD-ACCLIMATION ON GSH, ANTIOXIDANT ENZYMES AND LIPID-PEROXIDATION IN BROWN ADIPOSE-TISSUE [J].
DEQUIROGA, GB ;
LOPEZTORRES, M ;
PEREZCAMPO, R ;
ABELENDA, M ;
NAVA, MP ;
PUERTA, ML .
BIOCHEMICAL JOURNAL, 1991, 277 :289-292
[10]   INCREASED DOPAMINE AND NOREPINEPHRINE RELEASE IN MEDIAL PREFRONTAL CORTEX INDUCED BY ACUTE AND CHRONIC STRESS - EFFECTS OF DIAZEPAM [J].
FINLAY, JM ;
ZIGMOND, MJ ;
ABERCROMBIE, ED .
NEUROSCIENCE, 1995, 64 (03) :619-628