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评价水生生物急性麻醉作用的关键身体残留物数据。

Evaluation of critical body residue data for acute narcosis in aquatic organisms.

机构信息

LS McCarty Scientific Research & Consulting, Newmarket, Ontario, Canada.

出版信息

Environ Toxicol Chem. 2013 Oct;32(10):2301-14. doi: 10.1002/etc.2289.

Abstract

The Environmental Residue Effects Database was evaluated to identify critical body residues of organic chemicals causing acute baseline neutral narcosis in aquatic organisms. Over 15 000 records for >400 chemicals were evaluated. Mean molar critical body residues in the final data set of 161 records for 29 chemicals were within published ranges but varied within and among chemicals and species (~3 orders of magnitude), and lipid normalization did not consistently decrease variability. All 29 chemicals can act as baseline neutral narcotics, but chemicals and/or their metabolites may also act by nonnarcotic modes of action. Specifically, nonnarcotic toxicity of polycyclic aromatic hydrocarbons and/or their biotransformation derivatives may be a significant source of variability. Complete testing of the narcosis-critical body residue hypothesis was confounded by data gaps for key toxicity modifying factors such as metabolite formation/toxicity, lipid content/composition, other modes of toxic action, and lack of steady-state status. Such problems impede determination of the precise, accurate toxicity estimates necessary for sound toxicological comparisons. Thus, neither the data nor the chemicals in the final data set should be considered definitive. Changes to testing designs and methods are necessary to improve data collection and critical body residue interpretation for hazard and risk assessment. Each of the toxicity metrics discussed-wet weight and lipid weight critical body residues, volume fraction in organism lipid, and chemical activity-has advantages, but all are subject to the same toxicity modifying factors.

摘要

环境残留效应数据库被评估,以确定导致水生生物急性基线中性麻醉的有机化学物质的关键体内残留。评估了超过 15000 条记录,涉及 400 多种化学物质。在最终数据集的 161 条记录中,29 种化学物质的平均摩尔关键体内残留处于已发表的范围内,但在化学物质和物种之间存在差异(~3 个数量级),并且脂质归一化并没有始终降低变异性。所有 29 种化学物质都可以作为基线中性麻醉剂,但化学物质及其代谢物也可能通过非麻醉作用模式起作用。具体而言,多环芳烃及其生物转化衍生物的非麻醉毒性可能是变异性的重要来源。由于关键毒性修饰因子(如代谢物形成/毒性、脂质含量/组成、其他毒性作用模式以及稳态状态)的数据差距,对麻醉临界体内残留假设的全面测试受到了混淆。这些问题阻碍了确定用于健全毒理学比较的精确、准确毒性估计的可能性。因此,最终数据集中的数据和化学物质都不应被视为确定无疑的。需要改变测试设计和方法,以改善数据收集和临界体内残留解释,用于危害和风险评估。讨论的每个毒性指标——湿重和脂重临界体内残留、生物体脂质中的体积分数和化学活性——都有其优势,但都受到相同的毒性修饰因子的影响。

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