Anguiano Gerardo, Llera-Herrera Raul, Rojas Emilio, Vazquez-Boucard Celia
Department of Environmental Management and Conservation, Toxicogenomic and Reproduction of Aquatic Organism Laboratory (CIBNOR), P.O. 128, La Paz, Baja California Sur, México.
Environ Toxicol Chem. 2007 Oct;26(10):2192-7. doi: 10.1897/06-377R3.1.
This study evaluated organismal toxicity, cytotoxicity, and genotoxicity and the filtration rate in response to different concentrations of subchronic lindane (gamma-hexachlorocyclohexane [gamma-HCH]), exposure (12 d) in adult Pacific oysters Crassostrea gigas. Oysters were exposed in vivo in laboratory aquaria to 10 different concentrations (0.0-10.0 mg/L) of gamma-HCH. The median lethal concentration (LC50) after 12 d was calculated as 2.22 mg/L. Cytotoxic effects were observed in hemocytes, where the mean cell viability was significantly decreased at 1.0 mg/L of gamma-HCH after 12 d. Genotoxicity of gamma-HCH measured by single cell gel electrophoresis assay, in hemocytes was evident at 0.7 mg/L of gamma-HCH after 12 d. After 4 h of exposure to gamma-HCH, filtration rates were reduced compared with controls to 65.8 and 38.2% at concentrations of 0.3 and 0.7 mg/L, respectively, and after 11 d of exposure, filtration rates were reduced to 60.4 and 30.9% at concentrations of 0.1 mg/L and higher. These results show the subchronic effects of gamma-HCH at different concentrations and effect sensitivities are categorized as filtration rate < genotoxicity < cytotoxicity < mortality. The relevance of integral toxicity evaluation, considering different endpoints from molecular, cellular, and individual levels is discussed.
本研究评估了成年太平洋牡蛎(太平洋牡蛎)在亚慢性林丹(γ-六氯环己烷[γ-HCH])不同浓度下暴露12天的机体毒性、细胞毒性、遗传毒性以及滤过率。将牡蛎在实验室水族箱中进行体内暴露,使其接触10种不同浓度(0.0 - 10.0毫克/升)的γ-HCH。12天后计算得出的半数致死浓度(LC50)为2.22毫克/升。在血细胞中观察到了细胞毒性效应,12天后,当γ-HCH浓度为1.0毫克/升时,平均细胞活力显著下降。通过单细胞凝胶电泳试验测定,12天后,当γ-HCH浓度为0.7毫克/升时,血细胞中的γ-HCH遗传毒性明显。暴露于γ-HCH 4小时后,与对照组相比,在浓度分别为0.3和0.7毫克/升时,滤过率分别降低至65.8%和38.2%;暴露11天后,在浓度为0.1毫克/升及更高时,滤过率分别降低至60.4%和30.9%。这些结果显示了不同浓度γ-HCH的亚慢性效应,效应敏感性分类为滤过率<遗传毒性<细胞毒性<死亡率。讨论了综合毒性评估的相关性,其中考虑了分子、细胞和个体水平的不同终点。