Cobalt Institute, 18 Jeffries Passage, Guildford, GU1 4AP, UK.
EBRC Consulting GmbH, Raffaelstraße 4, 30177, Hannover, Germany.
Regul Toxicol Pharmacol. 2022 Apr;130:105127. doi: 10.1016/j.yrtph.2022.105127. Epub 2022 Feb 3.
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.
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。