Department of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Department of Environmental Science and Engineering, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Arch Toxicol. 2021 May;95(5):1547-1572. doi: 10.1007/s00204-021-03028-w. Epub 2021 Mar 26.
The toxic metalloid inorganic arsenic (iAs) is widely distributed in the environment. Chronic exposure to iAs from environmental sources has been linked to a variety of human diseases. Methylation of iAs is the primary pathway for metabolism of iAs. In humans, methylation of iAs is catalyzed by arsenic (+ 3 oxidation state) methyltransferase (AS3MT). Conversion of iAs to mono- and di-methylated species (MAs and DMAs) detoxifies iAs by increasing the rate of whole body clearance of arsenic. Interindividual differences in iAs metabolism play key roles in pathogenesis of and susceptibility to a range of disease outcomes associated with iAs exposure. These adverse health effects are in part associated with the production of methylated trivalent arsenic species, methylarsonous acid (MAs) and dimethylarsinous acid (DMAs), during AS3MT-catalyzed methylation of iAs. The formation of these metabolites activates iAs to unique forms that cause disease initiation and progression. Taken together, the current evidence suggests that methylation of iAs is a pathway for detoxification and for activation of the metalloid. Beyond this general understanding of the consequences of iAs methylation, many questions remain unanswered. Our knowledge of metabolic targets for MAs and DMAs in human cells and mechanisms for interactions between these arsenicals and targets is incomplete. Development of novel analytical methods for quantitation of MAs and DMAs in biological samples promises to address some of these gaps. Here, we summarize current knowledge of the enzymatic basis of MAs and DMAs formation, the toxic actions of these metabolites, and methods available for their detection and quantification in biomatrices. Major knowledge gaps and future research directions are also discussed.
有毒的类金属无机砷(iAs)广泛分布于环境中。从环境来源慢性暴露于 iAs 已与多种人类疾病相关联。iAs 的甲基化是 iAs 代谢的主要途径。在人类中,iAs 的甲基化由砷(+3 氧化态)甲基转移酶(AS3MT)催化。将 iAs 转化为单甲基化和二甲基化产物(MAs 和 DMAs),通过增加砷的全身清除率来解毒 iAs。iAs 代谢的个体间差异在与 iAs 暴露相关的一系列疾病结果的发病机制和易感性中起着关键作用。这些不良健康影响部分与 AS3MT 催化 iAs 甲基化过程中产生的三价甲基砷物种、甲基胂酸(MAs)和二甲基胂酸(DMAs)有关。这些代谢物的形成将 iAs 激活为引起疾病起始和进展的独特形式。总之,目前的证据表明,iAs 的甲基化是解毒和金属激活的途径。除了对 iAs 甲基化后果的一般理解之外,仍有许多问题尚未得到解答。我们对人类细胞中 MAs 和 DMAs 的代谢靶标以及这些砷化合物与靶标之间相互作用的机制知之甚少。开发用于定量生物样本中 MAs 和 DMAs 的新型分析方法有望解决其中的一些差距。在这里,我们总结了 MAs 和 DMAs 形成的酶学基础、这些代谢物的毒性作用以及在生物基质中检测和定量这些代谢物的可用方法的最新知识。还讨论了主要的知识差距和未来的研究方向。