Department of Biology, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Ecotoxicol Environ Saf. 2011 Sep;74(6):1586-94. doi: 10.1016/j.ecoenv.2011.04.025. Epub 2011 May 6.
The sub-lethal effects induced by the non-steroidal anti-inflammatory drug ((NSAID) ibuprofen (IBU; ((±)-2-(p-isobutylphenyl) propionic acid))) were investigated using a battery of biomarkers on the freshwater bivalve Dreissena polymorpha. According to the results from a semi-static in vivo approach, mussels were exposed for 96 h to increasing levels of environmentally relevant IBU concentrations (0.2, 2 and 8 μg/l, corresponding to 1, 9 and 35 nM, respectively). Cyto-genotoxicity was evaluated via the single cell gel electrophoresis (SCGE) assay, the DNA diffusion assay, the micronucleus test (MN test) and lysosome membrane stability (Neutral Red Retention Assay) in mussel hemocytes. In addition, the activities of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx) and the phase II detoxifying enzyme glutathione S-transferase (GST) were measured in the cytosolic fraction that was extracted from a pool of entire bivalves to determine whether the oxidative status was imbalanced. The biomarker battery pointed out a slight cyto-genotoxicity on zebra mussel hemocytes at the IBU concentration of 0.2 μg/l, with higher IBU concentrations able to significantly increase both genetic and cellular damage. In addition, IBU seems to have a considerable effect on the activities of antioxidant and detoxifying enzymes as shown in the exposed specimens' notable oxidative status imbalances.
采用一系列生物标志物,研究了非甾体抗炎药((NSAID)布洛芬(IBU;(±)-2-(对异丁基苯基)丙酸))对淡水双壳类贻贝多毛虫(Dreissena polymorpha)的亚致死效应。根据半静态体内方法的结果,贻贝在 96 小时内暴露于不同浓度的环境相关 IBU 浓度(0.2、2 和 8 μg/l,分别对应于 1、9 和 35 nM)。通过单细胞凝胶电泳(SCGE)试验、DNA 扩散试验、微核试验(MN 试验)和溶酶体膜稳定性(中性红保留试验)评估细胞遗传毒性,在贻贝血细胞中进行。此外,在从整个双壳类动物中提取的细胞溶质部分中测量了过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和 II 期解毒酶谷胱甘肽 S-转移酶(GST)的活性,以确定氧化状态是否失衡。生物标志物组合指出,在 IBU 浓度为 0.2 μg/l 时,斑马贻贝血细胞有轻微的细胞遗传毒性,较高的 IBU 浓度能够显著增加遗传和细胞损伤。此外,IBU 似乎对抗氧化和解毒酶的活性有相当大的影响,如暴露标本明显的氧化状态失衡所示。