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对鱼类胚胎急性毒性进行广泛综述以预测全球化学品统一分类和标签制度(GHS)急性全身毒性类别。

Extensive review of fish embryo acute toxicities for the prediction of GHS acute systemic toxicity categories.

作者信息

Scholz Stefan, Ortmann Julia, Klüver Nils, Léonard Marc

机构信息

UFZ - Helmholtz Centre for Environmental Research, Department of Bioanalytical Ecotoxicology, Permoserstr. 15, 04318 Leipzig, Germany.

UFZ - Helmholtz Centre for Environmental Research, Department of Bioanalytical Ecotoxicology, Permoserstr. 15, 04318 Leipzig, Germany.

出版信息

Regul Toxicol Pharmacol. 2014 Aug;69(3):572-9. doi: 10.1016/j.yrtph.2014.06.004. Epub 2014 Jun 11.

DOI:10.1016/j.yrtph.2014.06.004
PMID:24929227
Abstract

Distribution and marketing of chemicals require appropriate labelling of health, physical and environmental hazards according to the United Nations global harmonisation system (GHS). Labelling for (human) acute toxicity categories is based on experimental findings usually obtained by oral, dermal or inhalative exposure of rodents. There is a strong societal demand for replacing animal experiments conducted for safety assessment of chemicals. Fish embryos are considered as alternative to animal testing and are proposed as predictive model both for environmental and human health effects. Therefore, we tested whether LC50s of the fish embryo acute toxicity test would allow effectively predicting of acute mammalian toxicity categories. A database of published fish embryo LC50 containing 641 compounds was established. For these compounds corresponding rat oral LD50 were identified resulting in 364 compounds for which both fish embryo LC50 and rat LD50 was available. Only a weak correlation of fish embryo LC50 and rat oral LD50 was obtained. Fish embryos were also not able to effectively predict GHS oral acute toxicity categories. We concluded that due to fundamental exposure protocol differences (single oral dose versus water-borne exposure) a reverse dosimetry approach is needed to explore the predictive capacity of fish embryos.

摘要

化学品的分销和销售需要根据联合国全球协调系统(GHS)对健康、物理和环境危害进行适当的标签标注。(人类)急性毒性类别的标签标注基于通常通过啮齿动物口服、皮肤或吸入暴露获得的实验结果。社会对替代用于化学品安全评估的动物实验有强烈需求。鱼类胚胎被视为动物试验的替代方法,并被提议作为环境和人类健康影响的预测模型。因此,我们测试了鱼类胚胎急性毒性试验的半数致死浓度(LC50)是否能有效预测哺乳动物急性毒性类别。建立了一个包含641种化合物的已发表鱼类胚胎LC50数据库。对于这些化合物,确定了相应的大鼠口服半数致死剂量(LD50),从而得到364种同时具备鱼类胚胎LC50和大鼠LD50数据的化合物。鱼类胚胎LC50与大鼠口服LD50之间仅呈现微弱的相关性。鱼类胚胎也无法有效预测GHS口服急性毒性类别。我们得出结论,由于基本暴露方案存在差异(单次口服剂量与水体暴露),需要采用反向剂量测定法来探究鱼类胚胎的预测能力。

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