Levander O A
Environ Health Perspect. 1977 Aug;19:159-64. doi: 10.1289/ehp.7719159.
In 1938, Moxon discovered that arsenic protected against selenium toxicity. Since that time it has been shown that this protective effect of arsenic against selenium poisoning can be demonstrated in many different animal species under a wide variety of conditions. Antagonistic effects between arsenic and selenium have also been noted in teratologic experiments. Early metabolic studies showed that arsenic inhibited the expiration of volatile selenium compounds by rats injected with acutely toxic doses of both elements. This was puzzling since pulmonary excretion had long been regarded as a means by which animals could rid themselves of excess selenium. However, later work demonstrated that arsenic increased the biliary excretion of selenium. Not only did arsenic stimulate the excretion of selenium in the bile, but selenium also stimulated the excretion of arsenic in the bile. This increased biliary excretion of selenium caused by arsenic provides a reasonable rationale for the ability of arsenic to counteract the toxicity of selenium, although the chemical mechanism by which arsenic does this is not certain. The most satisfactory explanation is that these two elements react in the liver to form a detoxication conjugate which is then excreted into the bile. This is consistent with the fact that both arsenic and selenium each increase the biliary excretion of the other. Several other metabolic interactions between arsenic and selenium have been demonstrated in vitro, but their physiological significance is not clear. Although arsenic decreased selenium toxicity under most conditions, there is a pronounced synergistic toxicity between arsenic and two methylated selenium metabolites, trimethylselenonium ion or dimethyl selenide. The ecological consequences of these synergisms are largely unexplored, although it is likely that selenium methylation occurs in the environment. All attempts to promote or prevent selenium deficiency diseases in animals by feeding arsenic have been unsuccessful. Over 30 years ago it was suggested that industrial hygienists use arsenic as a tonic to prevent or cure selenium poisoning in workers exposed to this hazard. Organic arsenical feed additives were tried as partial antidotes against selenium poisoning in livestock raised in seleniferous agricultural areas but were not found to be practical.
1938年,莫克森发现砷可预防硒中毒。自那时起,已表明在多种条件下,许多不同动物物种都能表现出砷对硒中毒的这种保护作用。在致畸实验中也注意到了砷和硒之间的拮抗作用。早期的代谢研究表明,给大鼠注射急性毒性剂量的砷和硒后,砷会抑制大鼠呼出挥发性硒化合物。这令人费解,因为长期以来肺排泄一直被视为动物排出过量硒的一种方式。然而,后来的研究表明,砷会增加硒的胆汁排泄。砷不仅刺激胆汁中硒的排泄,硒也刺激胆汁中砷的排泄。砷导致的这种胆汁中硒排泄增加,为砷抵消硒毒性的能力提供了合理的解释,尽管砷这样做的化学机制尚不确定。最令人满意的解释是,这两种元素在肝脏中发生反应形成一种解毒共轭物,然后排泄到胆汁中。这与砷和硒都会增加彼此胆汁排泄的事实是一致的。在体外还证明了砷和硒之间的其他几种代谢相互作用,但其生理意义尚不清楚。尽管在大多数情况下砷会降低硒的毒性,但砷与两种甲基化硒代谢物——三甲基硒离子或二甲基硒化物之间存在明显的协同毒性。这些协同作用的生态后果在很大程度上尚未得到探索,尽管环境中可能会发生硒甲基化。所有通过喂食砷来促进或预防动物硒缺乏疾病的尝试均未成功。30多年前有人建议,工业卫生学家使用砷作为滋补剂,以预防或治疗接触此危害的工人的硒中毒。有机砷饲料添加剂曾被尝试作为在富硒农业地区饲养的牲畜硒中毒的部分解毒剂,但未发现其具有实用性。