Richardson Bruce J, Mak Eva, De Luca-Abbott Sharon B, Martin Michael, McClellan Katherine, Lam Paul K S
Department of Biology and Chemistry, Research Centre for Coastal Pollution and Conservation, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong.
Mar Pollut Bull. 2008;57(6-12):503-14. doi: 10.1016/j.marpolbul.2008.02.032. Epub 2008 May 21.
Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCs) are generally present in the marine environment in complex mixtures. The ecotoxicological nature of contaminant interactions, however, is poorly understood, with most scientific observations derived from single contaminant exposure experiments. The objective of this experiment was to examine dose-response relationships between antioxidant parameters and body contaminant levels in mussels exposed to different exposure regimes under laboratory conditions. Accordingly, the green-lipped mussel, Perna viridis, was challenged with a mixture of PAHs (anthracene, fluoranthene, pyrene, benzo[a]pyrene) and OC pesticides (alpha-HCH, aldrin, dieldrin, p,p'-DDT) over a 4 week period. Contaminants were delivered under four different dosing regimes, with all treatments receiving the same total contaminant load by the end of the exposure period. Antioxidant biomarkers were measured after 1, 2, 3 and 4 weeks, including glutathione (GSH), gluathione-S-transferase (GST), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR) and lipid peroxidase (LPO). GST and CAT were induced in hepatic tissues in most of the exposure regimes, with the majority of significant induction occurring in a constant exposure regime and a two-step alternate exposure regime. Significant differences among exposure regimes were detected in the body burden of contaminants after 28 days. Hepatic CAT and GSH are proposed as potentially useful biomarkers as they showed good correlation with target contaminants and were not readily affected by different dosing patterns.
多环芳烃(PAHs)和有机氯农药(OCs)通常以复杂混合物的形式存在于海洋环境中。然而,污染物相互作用的生态毒理学性质却鲜为人知,大多数科学观察结果来自单一污染物暴露实验。本实验的目的是研究在实验室条件下,暴露于不同暴露方案的贻贝中抗氧化参数与体内污染物水平之间的剂量反应关系。因此,绿唇贻贝(Perna viridis)在4周的时间内受到多环芳烃(蒽、荧蒽、芘、苯并[a]芘)和有机氯农药(α-六氯环己烷、艾氏剂、狄氏剂、p,p'-滴滴涕)混合物的挑战。污染物在四种不同的给药方案下投放,所有处理在暴露期结束时接受相同的总污染物负荷。在第1、2、3和4周后测量抗氧化生物标志物,包括谷胱甘肽(GSH)、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)和脂质过氧化物酶(LPO)。在大多数暴露方案中,肝组织中的GST和CAT被诱导,大多数显著诱导发生在持续暴露方案和两步交替暴露方案中。28天后,在不同暴露方案之间检测到污染物体内负荷存在显著差异。肝CAT和GSH被认为是潜在有用的生物标志物,因为它们与目标污染物显示出良好的相关性,并且不容易受到不同给药模式的影响。