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对 1990-2018 年铝盐遗传毒理学文献的批判性评价。

Critical review of the publications on the genotoxicology of aluminium salts: 1990-2018.

机构信息

CEHTRA SAS, 15 rue Aristide Briand, Cenon, Bordeaux, France.

出版信息

Mutagenesis. 2021 May 31;36(2):109-127. doi: 10.1093/mutage/geab008.

Abstract

Since the mid-1970s, there have been many reports that purport to implicate aluminium in the aetiology of neurodegenerative disease. After several decades of research, the role of aluminium in such disease remains controversial and is not the subject of this review. However, if aluminium is implicated in such disease then it follows that there must be a toxicological mechanism or mode of action, and many researchers have investigated various potential mechanisms including the involvement of oxidative damage, cytotoxicity and genotoxicity. This paper reviews many of the publications of studies using various salts of aluminium and various genotoxicity end points, both in vitro and in vivo, with a focus on oxidative damage. The conclusion of this review is that the majority, if not all, of the publications that report positive results have serious technical flaws and/or implausible findings and consequently should contribute little or no weight to a weight of evidence (WoE) argument. There are many high-quality, Good Laboratory Practice (GLP)-compliant genotoxicity studies, that follow relevant OECD test guidelines and the European Chemicals Agency (ECHA) integrated mutagenicity testing strategy, on several salts of aluminium; all demonstrate clear negative results for both in vitro and in vivo genotoxicity. In addition, the claim for an oxidative mode of action for aluminium can be shown to be spurious. This review concludes that there are no reliable studies that demonstrate a potential for genotoxicity, or oxidative mode of action, for aluminium.

摘要

自 20 世纪 70 年代中期以来,有许多报道声称铝与神经退行性疾病的病因有关。经过几十年的研究,铝在这类疾病中的作用仍然存在争议,也不是本次综述的主题。然而,如果铝与这类疾病有关,那么必然存在一种毒理学机制或作用模式,许多研究人员已经研究了各种潜在的机制,包括氧化损伤、细胞毒性和遗传毒性的参与。本文综述了许多使用各种铝盐和各种遗传毒性终点的研究出版物,这些研究既有体外研究也有体内研究,重点是氧化损伤。本文的结论是,大多数(如果不是全部)报告阳性结果的出版物都存在严重的技术缺陷和/或不可信的发现,因此对证据权重(WoE)的论证几乎没有或没有贡献。有许多高质量、符合良好实验室规范(GLP)的遗传毒性研究,遵循相关的经合组织测试指南和欧洲化学品管理局(ECHA)的综合致突变性测试策略,对几种铝盐进行了研究;所有研究都对体外和体内遗传毒性均显示出明确的阴性结果。此外,铝的氧化作用模式的说法也可以被证明是虚假的。本综述得出结论,没有可靠的研究表明铝具有遗传毒性或氧化作用模式的潜力。

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