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Antioxidant responses to benzo[a]pyrene and Aroclor 1254 exposure in the green-lipped mussel, Perna viridis

机译:绿唇贻贝Perna viridis对苯并[a] re和Aroclor 1254暴露的抗氧化反应

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In this study, the green-lipped mussel, Perna viridis (L.), was exposed to two concentrations of benzo[a]pyrene (B[a]P) (0.3 μg l~(-1); 3 μg l~(-1)) and two concentrations of Aroclor 1254 (0.5 μg l~(-1); 5 μg l~(-1)). In addition, a mixture of the contaminants was used (0.3 μg l~(-1) B[a]P + 0.5 μg l~(-1) Aroclor 1254; 3 μg l~(-1) B[a]P + 5 μg l~(-1) Aroclor 1254). All concentrations were nominal. A suite of enzymes [glutathione S transferase (GST), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reduc-tase (GR)], glutathione (GSH) level and lipid peroxidation (LPO) in the mussel gill and hepatopancreas were monitored over 18 days. CAT and GSH in gill tissue were positively correlated with concentration of Aroclor 1254. Activity of hepatic GST and SOD was significantly related to body burden of Aroclor 1254. LPO, GR and GPx in gill and hepatopancreas and hepatic GST were positively correlated with B[a]P concentration. The results indicate the importance of using biomarkers specific to the type of contaminant(s) that are likely to be present. Controlled laboratory experiments, such as this study, are useful in ascertaining biomarkers suitable for use with complex contaminant mixtures in the marine environment.
机译:在这项研究中,青唇贻贝Perna viridis(L.)暴露于两种浓度的苯并[a] py(B [a] P)(0.3μgl〜(-1); 3μgl〜( -1))和两种浓度的Aroclor 1254(0.5μgl〜(-1); 5μgl〜(-1))。此外,还使用了污染物的混合物(0.3μgl〜(-1)B [a] P + 0.5μgl〜(-1)Aroclor 1254; 3μgl〜(-1)B [a] P + 5μgl〜(-1)Aroclor 1254)。所有浓度均为标称值。一组酶[谷胱甘肽S转移酶(GST),超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽过氧化物酶(GPx),谷胱甘肽还原酶(GR)],谷胱甘肽(GSH)水平和脂质过氧化(LPO)在18天内对贻贝were和肝胰腺进行了监测。 g组织中的CAT和GSH与Aroclor 1254的浓度呈正相关。肝GST和SOD的活性与Aroclor 1254的身体负荷呈显着相关。g和肝胰腺中的LPO,GR和GPx以及肝GST与B [a]呈正相关。 ] P浓度。结果表明使用针对可能存在的污染物类型的特异性生物标志物的重要性。诸如本研究之类的受控实验室实验可用于确定适合与海洋环境中的复杂污染物混合物一起使用的生物标志物。

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