Arsenic essentiality: A role affecting methionine metabolism†‡

Eric O. Uthus
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引用次数: 45

Abstract

Although there is no known biological function of arsenic, considerable evidence suggests that arsenic has a physiological role related to methionine metabolism. In early studies using amino acid-based diets, it was found that arsenic deprivation had little effect on growth in rats fed adequate methionine. However, in rats fed suboptimal methionine, arsenic deprivation resulted in a significant reduction in body weight. Other studies showed that feeding methyl depletors caused severe signs of arsenic deprivation. Because it was found that alteration in methionine status or methyl metabolism affected signs of arsenic deprivation, and that many of these signs were related to methionine or methyl metabolism, it was hypothesized that arsenic has a physiological role affecting methionine metabolism. In animal studies testing this hypothesis, it was shown that arsenic deprivation reduces the hepatic concentration of S-adenosylmethionine. Additionally, arsenic status affects DNA methylation in animal and cell culture models; very low or high doses of arsenic, compared with control amounts, result in an apparent hypomethylation of DNA. Because global DNA hypomethylation is associated with an increased incidence of cancer, we tested whether dietary arsenic (deficient, adequate, or excess; 0, 0.5 or 50 μg arsenic/g diet, respectively) would affect the formation of aberrant crypts in rats treated with the carcinogen dimethylhydrazine. Aberrant crypts are preneoplastic lesions that have been associated with colon carcinomas. More aberrant crypts were observed in rats fed the high amount of dietary arsenic compared to those fed adequate arsenic. The number of aberrant crypts in the arsenic-deprived group also tended to be higher than those found in rats fed adequate arsenic. Thus, many findings indicate that arsenic plays a role in methionine/methyl metabolism; however, the site of action of arsenic remains unknown. Possibly, arsenic is instrumental in maintaining the metabolic pool of S-adenosylmethionine. These results show that compared to controlled amounts, having too little or too much arsenic in the diet is harmful. That is, there is an amount of dietary arsenic that is not only not harmful, but beneficial. J. Trace Elem. Exp. Med. 16:345–355, 2003. Published 2003 Wiley-Liss, Inc.
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砷的重要性:影响蛋氨酸代谢的作用††
尽管目前还没有已知的砷的生物学功能,但有相当多的证据表明,砷具有与蛋氨酸代谢有关的生理作用。在使用氨基酸饮食的早期研究中,发现缺砷对喂食充足蛋氨酸的大鼠的生长几乎没有影响。然而,在喂食次优甲硫氨酸的大鼠中,缺砷可显著降低体重。其他研究表明,喂食甲基消耗物会导致砷缺乏的严重迹象。由于发现甲硫氨酸状态或甲基代谢的改变会影响砷缺乏的迹象,并且其中许多迹象与甲硫氨酸或甲基代谢有关,因此假设砷在影响甲硫氨酸代谢方面具有生理作用。在验证这一假设的动物研究中,研究表明,缺砷会降低肝脏中S-腺苷甲硫氨酸的浓度。此外,砷状态影响动物和细胞培养模型中的DNA甲基化;与对照量相比,非常低或高剂量的砷会导致DNA明显的低甲基化。由于整体DNA低甲基化与癌症发病率的增加有关,我们测试了饮食中的砷(不足、充足或过量;分别为0、0.5或50μg砷/g饮食)是否会影响接受致癌物二甲基肼治疗的大鼠异常隐窝的形成。异常隐窝是与结肠癌相关的癌前病变。与喂食足量砷的大鼠相比,喂食大量砷的大白鼠中观察到更多的异常隐窝。缺砷组异常隐窝的数量也往往高于喂食充足砷的大鼠。因此,许多研究结果表明,砷在甲硫氨酸/甲基代谢中发挥作用;然而,砷的作用部位仍然未知。砷可能有助于维持S-腺苷甲硫氨酸的代谢库。这些结果表明,与控制量相比,饮食中砷含量过少或过多是有害的。也就是说,饮食中有一定量的砷不仅无害,而且有益。J.Trace Elem。《实验医学》,16:345–3552003。出版于2003年,Wiley-Liss,股份有限公司。
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International Society For Trace Element Research In Humans (ISTERH) Seventh International Conference, Bangkok, Thailand, November 7–12, 2004 Response† Erratum Fluoride: A toxic or therapeutic agent in the treatment of osteoporosis? Interleukin-1α, tumor necrosis factor-α, and interleukin-12 secreted by zinc-induced murine macrophages in vivo and in vitro
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