Joint toxicity on hepatic detoxication enzymes in goldfish (Carassius auratus) exposed to binary mixtures of lead and paraquat

被引:5
|
作者
Xu, Xiaoming [1 ,2 ]
Cui, Zhaojie [1 ]
Wang, Shanshan [2 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Shandong, Peoples R China
[2] Shandong Jianzhu Univ, Sch Municipal & Environm Engn, Jinan 250101, Shandong, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Joint effect; Lead; Paraquat; Biotransformation enzymes; Biomarker; ZEBRAFISH DANIO-RERIO; GLUTATHIONE-S-TRANSFERASE; INDUCED OXIDATIVE STRESS; UDP-GLUCURONOSYLTRANSFERASES UGTS; TROUT ONCORHYNCHUS-MYKISS; HEAVY-METALS; DROSOPHILA-MELANOGASTER; EROD ACTIVITY; DNA-DAMAGE; BIOCHEMICAL BIOMARKERS;
D O I
10.1016/j.etap.2018.06.005
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Compared to single exposure, chemical mixtures might induce joint toxicity including additive, synergistic and antagonistic effects on both organisms and environment. Owing to the specific toxicity of oxidative stress and binding to proteins, lead (Pb) is generally recognized a non-essential and threatening heavy metal to animals and human. Paraquat (PQ) is a widely used herbicide in agriculture and can trigger oxidative stress as well as Pb. Little information was available about joint effects of the two chemicals on toxicological responses in organisms, especially in fish. In our present study, goldfish (Carassius auratus) were randomly exposed to single and combined experiments with different concentrations of Pb and PQ for 28 days. Activities of four enzyme biomarkers in liver, ethoxyresorufin-O-deethylase (EROD), 7-benzyloxy-4-trifluoromethyl-coumarin-O-debenzyloxylase (BFCOD), glutathione-S-transferase (GST) and UDP-glucuronosyltransferase (UGT) were evaluated in each experimental group on day 14 and 28. The results showed four enzyme levels were markedly reduced with the increase of concentrations in mixtures and prolonged exposure. The inhibitory EROD and BFCOD activities were not significantly changed in goldfish following PQ-treated groups with or without 0.5 mg/L Pb, which indicated PQ has more inhibitory toxicity on CYP450 enzymes than Pb in co-exposure groups. However, the reduced values of GST were observed only in the combinations containing high doses of Pb or PQ during experimental periods. Although the responses of UGT activity were similar to GST on 14th day, all combinations of Pb and PQ generated stronger inhibitions on UGT activities compared to individual Pb and PQ-treated group. These results suggested that combined exposure of Pb and PQ have more inhibitory toxicity on phase I enzymes than phase II enzymes.
引用
收藏
页码:60 / 68
页数:9
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