Decreased susceptibility to lipid peroxidation of Goto-Kokizaki rats:: Relationship to mitochondrial antioxidant capacity

被引:37
作者
Ferreira, FML [1 ]
Palmeira, CM
Matos, MJ
Seiça, R
Santos, MS
机构
[1] Univ Coimbra, Dept Zool, Ctr Neurosci Coimbra, P-3004517 Coimbra, Portugal
[2] Univ Coimbra, Dept Biochem, P-3004517 Coimbra, Portugal
[3] Univ Coimbra, Fac Med, P-3004517 Coimbra, Portugal
关键词
Goto-Kakizaki rats; type 2 diabetes mellitus; mitochondria; respiratory index; lipid peroxidation; antioxidant enzymes; alpha-tocopherol;
D O I
10.1016/S0024-3205(99)00332-X
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The respiratory function and the antioxidant capacity of liver mitochondrial preparations isolated from Goto-Kakizaki non-insulin dependent diabetic rats and from Wister control rats, with the age of 6 months, were compared. It was found that Goto-Kakizaki mitochondrial preparations presented a higher coupling between oxidative and phosphorylative systems, compared to non-diabetic preparations. Goto-Kakizaki mitochondria presented a lower susceptibility to lipid peroxidation induced by ADP/Fe2+, as evaluated by the formation of thiobarbituric acid substances. The decreased susceptibility to peroxidation in diabetic rats was correlated with an increase in mitochondrial vitamin E (alpha-tocopherol) content and GSH/GSSG ratio. Moreover, the glutathione reductase activity was significantly increased, whereas the glutathione peroxidase was decreased. Superoxide dismutase activity was unchanged in diabetic rats. Fatty acid analyses showed that the content in polyunsaturated fatty acids of Goto-Kakizaki mitochondrial membranes was significantly higher compared to controls. These results indicate that the lower susceptibility to lipid peroxidation of mitochondria from diabetic rats was related to their antioxidant defense systems, and may correspond to an adaptative response of the cells against oxidative stress in the early phase of diabetes.
引用
收藏
页码:1013 / 1025
页数:13
相关论文
共 45 条
[1]   FORMATION AND REDUCTION OF GLUTATHIONE-PROTEIN MIXED DISULFIDES DURING OXIDATIVE STRESS - A STUDY WITH ISOLATED HEPATOCYTES AND MENADIONE (2-METHYL-1,4-NAPHTHOQUINONE) [J].
BELLOMO, G ;
MIRABELLI, F ;
DIMONTE, D ;
RICHELMI, P ;
THOR, H ;
ORRENIUS, C ;
ORRENIUS, S .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (08) :1313-1320
[2]   CEREBRAL FUNCTION IN DIABETES-MELLITUS [J].
BIESSELS, GJ ;
KAPPELLE, AC ;
BRAVENBOER, B ;
ERKELENS, DW ;
GISPEN, WH .
DIABETOLOGIA, 1994, 37 (07) :643-650
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]   MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE - GENERAL PROPERTIES AND EFFECT OF HYPERBARIC-OXYGEN [J].
BOVERIS, A ;
CHANCE, B .
BIOCHEMICAL JOURNAL, 1973, 134 (03) :707-716
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   A MILD, RAPID, AND EFFICIENT METHOD OF LIPID EXTRACTION FOR USE IN DETERMINING VITAMIN-E LIPID RATIOS [J].
BURTON, GW ;
WEBB, A ;
INGOLD, KU .
LIPIDS, 1985, 20 (01) :29-39
[7]  
Calberg I., 1985, METHOD ENZYMOL, V113, P484
[8]  
CHANCE B, 1956, ADV ENZYMOL REL S BI, V17, P65
[9]   DIRECT MEASUREMENT OF LIPID-PEROXIDATION IN SUBMITOCHONDRIAL PARTICLES [J].
DEHINGH, YCM ;
MEYER, J ;
FISCHER, JC ;
BERGER, R ;
SMEITINK, JAM ;
DENKAMP, JAFO .
BIOCHEMISTRY, 1995, 34 (39) :12755-12760
[10]  
Duhault J, 1997, THERAPIE, V52, P375