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采用分级方法研究钴物质的吸入毒性。第 3 级:急性吸入暴露后的炎症反应与较低级别数据相关。

A tiered approach to investigate the inhalation toxicity of cobalt substances. Tier 3: Inflammatory response following acute inhalation exposure correlates with lower tier data.

机构信息

Cobalt Institute, 18 Jeffries Passage, Guildford, GU1 4AP, UK.

EBRC Consulting GmbH, Raffaelstraße 4, 30177, Hannover, Germany.

出版信息

Regul Toxicol Pharmacol. 2022 Apr;130:105127. doi: 10.1016/j.yrtph.2022.105127. Epub 2022 Feb 3.

DOI:10.1016/j.yrtph.2022.105127
PMID:35124137
Abstract

In vitro studies have shown that cobalt substances predominantly induce pre-inflammatory biomarkers, resulting in a grouping of substances either predicted to cause inflammation following inhalation, or those with a different reactivity profile (poorly-reactive). There is a lack of data on whole-organ lung responses following inhalation of these substances, especially relating to the poorly-reactive group. It is of interest to generate tissue-specific histopathological correlation to better ascertain the predictive nature of the lower tier tests (i.e. tier 1 - bioelution, tiers 2a and b - in vitro markers and ToxTracker testing), in order to understand the type of effects caused by the poorly-reactive group and to gauge long-term effects. Eight cobalt substances were tested in vivo in a customized 4-h toxicity test; with animals sacrificed up to 14-days post-exposure. Histopathological severity scores were assigned based on inflammatory and pre-carcinogenic markers. A clear pattern emerged, with the reactive substances causing a persistent increase in one or more of the selected markers, and absence of these markers with poorly-reactive substances. Longer-term studies should be conducted to investigate the repeated dose effects of the poorly-reactive substances.

摘要

体外研究表明,钴物质主要诱导前炎症生物标志物,导致一组物质要么被预测为吸入后会引起炎症,要么具有不同的反应性特征(反应性差)。对于这些物质吸入后对整个器官肺部的反应,缺乏数据,特别是对于反应性差的组。产生组织特异性组织病理学相关性很重要,以便更好地确定较低层次测试(即第 1 层-生物洗脱,第 2a 和 b 层-体外标志物和 ToxTracker 测试)的预测性质,以了解反应性差的组引起的效应类型,并评估长期效应。在定制的 4 小时毒性试验中,对 8 种钴物质进行了体内测试;在暴露后最多 14 天处死动物。根据炎症和前致癌标志物对组织病理学严重程度评分进行赋值。出现了一个清晰的模式,反应性物质导致一个或多个选定标志物持续增加,而反应性差的物质则不存在这些标志物。应进行更长期的研究,以调查反应性差的物质的重复剂量效应。

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