Lipid peroxidation, antioxidant enzymes, and benzo[a]pyrene-quinones in the blood of rats treated with benzo[a]pyrene

被引:88
|
作者
Kim, HS [1 ]
Kwack, SJ [1 ]
Lee, BM [1 ]
机构
[1] Sungkyunkwan Univ, Coll Pharm, Div Toxicol, Suwon 440746, Kyunggi Do, South Korea
关键词
lipid peroxidation; antioxidant enzymes; benzo[a]pyrene-quinones;
D O I
10.1016/S0009-2797(00)00177-0
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 lipid peroxidation (as malondialdehyde, MDA), activities of superoxide dismutase (SOD) and catalase (CAT), and benzo[a]pyrene (BaP) metabolites were investigated in sera and erythrocytes of male Sprague-Dawley rats treated with BaP (20 mg per rat). MDA levels were significantly increased in sera (16.98 +/- 3.29 nmol/ml serum, P < 0.05) 12 h after BaP treatment and persisted up to 96 h (13.80 +/- 1.65 nmol/ml serum, P < 0.05), but no significant change in NIDA levels was observed in erythrocytes. SOD and CAT activities were significantly increased in erythrocytes shortly after BaP exposure, and they were slightly decreased in sera, indicating an inverse correlation between lipid peroxidation and antioxidant enzyme activity. BaP and BaP-quinones (BaP-1,6-quinone and BaP-3,6-quinone) were measured in sera during the study period. A rapid increase of unmetabolized BaP was observed in sera (41.27 +/- 4.14 pmol/ml serum) 3 h after BaP treatment, reaching a peak at 6 h (48.56 +/- 4.62 pmol/ml serum) followed by a sharp decrease. Formation of the BaP-1,6-quinone and BaP-3,6-quinone started in sera 3 h after BaP treatment, reached a peak at 24 h (7.23 +/- 1.02 pmol/ml serum) and 12 h (9.20 +/- 0.98 pmol/ml serum), respectively, and then decreased gradually. The time-dependent pattern of serum lipid peroxidation and the level of erythrocyte antioxidant enzymes were shown to be related to the concentrations of the BaP-quinone metabolites. These results suggest that BaP treatment, probably via the formation of BaP-quinones, oxidatively altered lipids and antioxidant enzymes in the blood, and might be associated with BaP-related vascular toxicity including carcinogenesis. (C) 2127 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:139 / 150
页数:12
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