根据农药对肝脏的累积风险评估,收集资料、描述危害特征及成立累积评估小组

Tamara Coja, Lena Brunner, Daniela Hofstädter, Melanie Kuffner, Ulrike Mayerhofer, Elke Rauscher-Gabernig, Hao Sun, Katharina Vejdovszky
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引用次数: 0

摘要

本报告的目的是收集各种农药及其代谢物对肝脏和胆囊的毒性作用的数据,并随后建立累积评估小组(CAGs),以便进行农药残留对肝脏的累积风险评估(CRA)。为此目的,查阅了一份先前确定的具体影响指标清单,以便从毒理学评估报告中检索相关数据。从监管文件中收集了62种优先农药活性物质和20种鉴定代谢物的毒理学数据。对于每种物质,为最敏感的特异效应指标推导出LOAEL。从最初定义的10种特定效应和各自的cag中,有7种是由活性物质和代谢物填充的:1)酶诱导的肥大,肝脏;2)肝细胞性脂肪改变和/或磷脂病;3)变性/细胞死亡,肝细胞;4)卟啉症、肝细胞症、胆管症;5)胆汁淤积,肝细胞,胆管;6)肿瘤前和肿瘤改变,肝细胞;7)胆管肿瘤改变。没有发现化合物填充先前定义的三种对胆囊的特定影响:1)侵蚀/溃疡,胆囊;2)胆囊结石;3)肿瘤改变,胆囊。强调了在不同cag中物质分配的确定不确定性。总体而言,该项目采用了报告中先前开发和描述的方法,用于确定对肝脏的特定影响,并提供了物质的全面危害特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Data collection, hazard characterisation and establishment of cumulative assessment groups in view of the cumulative risk assessment of pesticides for liver

Data collection, hazard characterisation and establishment of cumulative assessment groups in view of the cumulative risk assessment of pesticides for liver

Data collection, hazard characterisation and establishment of cumulative assessment groups in view of the cumulative risk assessment of pesticides for liver

Data collection, hazard characterisation and establishment of cumulative assessment groups in view of the cumulative risk assessment of pesticides for liver

The aim of the present report is to collect data on toxic effects in the liver and gallbladder from various pesticides and their metabolites and, subsequently, to establish cumulative assessment groups (CAGs), in view of performing cumulative risk assessment (CRA) of pesticide residues for liver. For this purpose, a list of previously defined indicators of the specific effects was consulted to retrieve the relevant data from toxicological assessment reports. Toxicological data from 62 prioritised pesticide active substances and 20 identified metabolites were collected from regulatory documents. For each substance, a LOAEL was derived for the most sensitive indicator(s) of the specific effect. From originally defined ten specific effects and the respective CAGs, seven were populated by active substances and metabolites: 1) hypertrophy due to enzymatic induction, liver; 2) fatty change and/or phospholipidosis, hepatocellular; 3) degeneration/cell death, hepatocellular; 4) porphyria, hepatocellular, biliary duct; 5) cholestasis, hepatocellular, biliary duct; 6) preneoplastic and neoplastic changes, hepatocellular; 7) neoplastic changes, biliary duct. No compounds were identified to populate three previously defined specific effects on gallbladder: 1) erosion/ulceration, gallbladder; 2) calculi, gallbladder; 3) neoplastic changes, gallbladder. The identified uncertainties in the allocation of the substances in the different CAGs were highlighted. Overall, this project utilises the methodology previously developed and described in the report dealing with the identification of specific effects on liver and it provides a comprehensive hazard characterisation of substances.

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