Chromium

R. Anderson
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Abstract

T wooxidation states of chromiumare considered tobe biologically and environmentally relevant based on their stability in the presence of water and oxygen. Compounds containing chromium(6+ ) are mutagenic and carcinogenic when inhaled and potentially when ingested orally in large quantity as well. Chromium as the trivalent will be the focus of this work as it was proposed to be an essential element for mammals ∼60 y ago; however, in the last 2 decades its status has been questioned. Chromium has been postulated to be involved in regulating carbohydrate and lipid (and potentially also protein) metabolism by enhancing insulin’s efficacy (1). However, in 2014, the European Food Safety Authority found no convincing evidence that chromium is an essential element (2). Dietary chromium apparently is absorbed via passive diffusion and the extent of absorption is low (∼1%). Chromium is maintained in the bloodstream bound to the protein transferrin. It is generally believed to be delivered to tissues by transferrin via endocytosis (1). No unambiguous animal model of chromium deficiency has been established (2). One limitation in characterizing chromium deficiency in humans is the lack of an accepted biomarker of chromium nutritional status. Attempts to identify a glucose tolerance factor have not provided a chemically defined functional compound that conforms with the proposed physiologic role of chromium as a facilitator of insulin action in vivo.
铬的氧化状态被认为是与生物和环境相关的,基于它们在水和氧存在下的稳定性。含铬(6+)的化合物在吸入时具有诱变性和致癌性,在大量口服时也可能具有致癌性。铬作为三价将是这项工作的重点,因为它在大约60年前被提出是哺乳动物的基本元素;然而,在过去的20年里,它的地位受到了质疑。铬被认为通过增强胰岛素的功效参与调节碳水化合物和脂质(也可能是蛋白质)的代谢(1)。然而,在2014年,欧洲食品安全局没有发现令人信服的证据表明铬是一种必需元素(2)。饮食中的铬显然是通过被动扩散吸收的,吸收程度很低(约1%)。铬在血液中与蛋白质转铁蛋白结合。一般认为,它是通过转铁蛋白通过内吞作用传递到组织中的(1)。目前还没有明确的铬缺乏动物模型(2)。表征人类铬缺乏的一个限制是缺乏公认的铬营养状态的生物标志物。试图确定葡萄糖耐量因子并没有提供一个化学定义的功能化合物,符合铬作为体内胰岛素作用的促进剂的生理作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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