Endocrine disruptive effects of inorganic arsenicals.

Teruaki Sakurai, Seiichiro Himeno
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Abstract

Although inorganic arsenicals are toxic and carcinogenic in humans, inorganic arsenite has recently emerged as a highly effective chemotherapeutic agent for acute promyelocytic leukemia (APL). Recently, the number of arsenic-related publications has greatly increased, but the effects of arsenicals on the endocrine system have not been well studied. A number of in vivo studies about only inorganic-arsenical-induced endocrine-disruptor-like effects have been conducted using mouse models, and they demonstrated that inorganic arsenicals might act as an estrogen-like chemical in vivo and induce some tumors in mice. In most mammalian species, however, inorganic arsenicals are enzymatically methylated as a detoxifying metabolic response. Thus, studies of endocrine disruptive effects of methylated arsenicals are also needed for a clinical understanding of this attractive metalloid in the near future.

无机砷对内分泌的干扰作用。
尽管无机砷对人体具有毒性和致癌性,但无机亚砷酸盐最近已成为急性早幼粒细胞白血病(APL)的一种高效化疗药物。近年来,与砷有关的出版物大量增加,但砷对内分泌系统的影响尚未得到很好的研究。许多关于无机砷诱导的内分泌干扰物样效应的体内研究已经在小鼠模型中进行了,他们证明无机砷可能在体内作为雌激素样化学物质,并在小鼠中诱导某些肿瘤。然而,在大多数哺乳动物物种中,无机砷作为一种解毒代谢反应被酶甲基化。因此,在不久的将来,还需要对甲基化砷的内分泌干扰效应进行研究,以便临床了解这种有吸引力的类金属。
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