Effects of vitamin A deficiency on selected xenobiotic-metabolizing enzymes and defenses against oxidative stress in mouse liver

被引:17
作者
Sohlenius-Sternbeck, AK
Appelkvist, EL
DePierre, JW [1 ]
机构
[1] Univ Stockholm, Wallenberg Lab, Dept Biochem, Biochem Toxicol Unit, S-10691 Stockholm, Sweden
[2] Karolinska Inst, Novum, Clin Res Ctr, S-14186 Huddinge, Sweden
关键词
vitamin A deficiency; mouse liver; xenobiotic-metabolizing enzymes; antioxidant defense; oxidative stress;
D O I
10.1016/S0006-2952(99)00337-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Male and female C57Bl/6 mice were rendered vitamin A-deficient, and the effects of this deficiency on certain xenobiotic-metabolizing enzymes and defenses against oxidative stress were examined. Vitamin A deficiency significantly increased the levels of DT-diaphorase, glutathione transferase, and catalase in the hepatic cytosolic fraction from male mice (5.2-, 1.6-, and 3.5-fold, respectively), as well as from female mice (4.8-, 3.3-, and 2.4-fold, respectively). In the hepatic mitochondrial fraction (containing peroxisomes) from male animals, the activities of urate oxidase and catalase were increased 3.4- and 1.7-fold, respectively. The activity of catalase in the mitochondrial fraction from female mice was not affected by vitamin A deficiency, whereas the activity of peroxisomal urate oxidase was increased 2.9-fold. The hepatic level of ubiquinone was increased somewhat. The significance of the increases observed here is presently unclear, but it may be speculated that vitamin A and/or its metabolites are somehow involved in the down-regulation of these proteins. Another possibility is that these enzymes are increased as a result of hepatic oxidative stress caused by vitamin A deficiency. However, vitamin A deficiency had no effect on the activity of superoxide dismutase in this study, whereas the activity of glutathione peroxidase was slightly decreased (27%) in the hepatic cytosolic fraction from male mice. In addition, the hepatic level of ol-tocopherol was decreased dramatically in the vitamin A-deficient animals. BIOCHEM PHARMACOL 59;4:377-383, 2000. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:377 / 383
页数:7
相关论文
共 37 条
[1]   DISTRIBUTION AND REDOX STATE OF UBIQUINONES IN RAT AND HUMAN TISSUES [J].
ABERG, F ;
APPELKVIST, EL ;
DALLNER, G ;
ERNSTER, L .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 295 (02) :230-234
[2]   EFFECTS OF CLOFIBRATE, PHTHALATES AND PROBUCOL ON UBIQUINONE LEVELS [J].
ABERG, F ;
ZHANG, YY ;
APPELKVIST, EL ;
DALLNER, G .
CHEMICO-BIOLOGICAL INTERACTIONS, 1994, 91 (01) :1-14
[3]   Increases in tissue levels of ubiquinone in association with peroxisome proliferation [J].
Aberg, F ;
Zhang, YY ;
Teclebrhan, H ;
Appelkvist, EL ;
Dallner, G .
CHEMICO-BIOLOGICAL INTERACTIONS, 1996, 99 (1-3) :205-218
[4]  
ANGERMULLER S, 1989, PROG HISTOCHEM CYTOC, V20, P1
[5]  
AYALOGU EO, 1988, ANN NUTR METAB, V32, P75, DOI 10.1159/000177411
[6]  
BERGMEYER HU, 1955, BIOCHEM Z, V327, P255
[7]   HEPATIC OXIDATIVE STRESS AND RELATED DEFENSES DURING TREATMENT OF MICE WITH ACETYLSALICYLIC-ACID AND OTHER PEROXISOME PROLIFERATORS [J].
CAI, YN ;
APPELKVIST, EL ;
DEPIERRE, JW .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1995, 10 (02) :87-94
[8]  
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[9]   HYDROPEROXIDE METABOLISM IN MAMMALIAN ORGANS [J].
CHANCE, B ;
SIES, H ;
BOVERIS, A .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :527-605
[10]  
DE LUCA LM, 1991, FASEB J, V5, P2924