A Common Adverse Outcome Pathway for Metal(loid)s Inducing Nephrotoxicity to Advance Next-Generation Risk Assessment of Chemical Mixtures.

IF 13.1 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Tessa Schillemans, Annick D van den Brand, Agneta Åkesson, Marcel J B Mengelers, Mirjam Luijten
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引用次数: 0

Abstract

Chronic exposure to the metal(loid)s arsenic, cadmium, lead, and mercury via contaminated food or drinking water may induce kidney toxicity, but there is little consensus on the biological processes involved. Health risk assessment of these substances is further complicated by coexposures and the sometimes unclear causal interpretation of population studies. To address these issues, we developed a common adverse outcome pathway (AOP) describing how these metal(loid)s can induce kidney toxicity. Upon identification of renal dysfunction resulting from proximal tubular damage as a common adverse outcome, we developed the AOP by collecting evidence from relevant (experimental) studies. Evaluation of the weight of evidence revealed a moderate to high confidence in this AOP. It enhances our mechanistic understanding of metal(loid)-induced kidney toxicity and provides scientific evidence for a causal relationship between the adverse effect and effect biomarkers. As such, this is an example of how AOPs can facilitate next-generation risk assessment of combined exposure to different contaminants.

一种常见的金属(样物质)诱导肾毒性的不良后果通路,以推进下一代化学混合物的风险评估。
通过受污染的食物或饮用水长期暴露于金属(如砷、镉、铅和汞)可能会引起肾毒性,但对所涉及的生物过程几乎没有共识。这些物质的健康风险评估因共同接触和人口研究有时不明确的因果解释而进一步复杂化。为了解决这些问题,我们开发了一种常见的不良结局途径(AOP),描述了这些金属(样蛋白)如何诱导肾毒性。在确定近端肾小管损害是常见的不良后果后,我们通过收集相关(实验)研究的证据开发了AOP。对证据权重的评估显示了对该AOP的中等到高的置信度。它增强了我们对金属(样蛋白)诱导的肾毒性的机制理解,并为不良反应和效应生物标志物之间的因果关系提供了科学证据。因此,这是AOPs如何促进下一代不同污染物联合暴露风险评估的一个例子。
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来源期刊
CiteScore
27.80
自引率
0.00%
发文量
53
期刊介绍: Since 1961, the Annual Review of Pharmacology and Toxicology has been a comprehensive resource covering significant developments in pharmacology and toxicology. The journal encompasses various aspects, including receptors, transporters, enzymes, chemical agents, drug development science, and systems like the immune, nervous, gastrointestinal, cardiovascular, endocrine, and pulmonary systems. Special topics are also featured in this annual review.
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