Department of Environmental, Occupational Health and Toxicology, Graduate School of Medical Sciences, Kitasato University.
Department of Health Administration, School of Allied Health Sciences, Kitasato University.
J Toxicol Sci. 2020;45(9):539-548. doi: 10.2131/jts.45.539.
We investigated the mechanism underlying intestinal cadmium (Cd) uptake based on the mediators (metal transporters) of essential elements, such as Fe, Zn, Cu, and Ca, under normal conditions in female rats. These elements interact with Cd uptake from the intestinal tract. Cd concentration at each site of the small intestine (duodenum, jejunum, and ileum) increased as Cd exposure increased. However, Cd concentration was the highest in the duodenum. The gene expression of ZIP14, DMT1, and ATP7A increased with increase in Cd concentration. Further, Cu concentration decreased as Cd concentration increased. In contrast, Fe concentration displayed a decreasing tendency with the increase in Cd concentration. The gene expression levels of ZIP14, DMT1, and ATP7A were positively correlated with Cd concentration. Immunohistochemical staining revealed the positive sites of ZIP14 and DMT1 scattered in the area adjacent to the goblet cells, resorbable epithelial cells, and lamina propria in the duodenum tissue, according to the increase in Cd concentration. Cd is induced to synthesize and bind to metallothionein (MT-I and -II) and accumulate in the intestinal tissues, mainly in the duodenum. Such findings suggest that Cd, a contaminant element, is taken up from the intestinal tract by multiple metal transporters such as Cu, Fe, and Zn, thereby involving in the intestinal Cd absorption.
我们研究了在女性大鼠正常条件下,基于必需元素(如铁、锌、铜和钙)的介导物(金属转运蛋白)的肠道镉(Cd)摄取机制。这些元素与从肠道摄取的 Cd 相互作用。随着 Cd 暴露的增加,小肠(十二指肠、空肠和回肠)各个部位的 Cd 浓度增加。然而,Cd 浓度在十二指肠中最高。随着 Cd 浓度的增加,ZIP14、DMT1 和 ATP7A 的基因表达增加。此外,随着 Cd 浓度的增加,Cu 浓度降低。相比之下,Fe 浓度随着 Cd 浓度的增加呈下降趋势。ZIP14、DMT1 和 ATP7A 的基因表达水平与 Cd 浓度呈正相关。免疫组织化学染色显示,根据 Cd 浓度的增加,ZIP14 和 DMT1 的阳性部位散在十二指肠组织中靠近杯状细胞、可吸收上皮细胞和固有层的区域。Cd 被诱导合成并与金属硫蛋白(MT-I 和 -II)结合并在肠道组织中积累,主要在十二指肠。这些发现表明,Cd 作为一种污染物元素,通过多种金属转运蛋白(如 Cu、Fe 和 Zn)从肠道摄取,从而参与肠道 Cd 吸收。