Department Food Safety, Federal Institute of Risk Assessment (BfR), Max-Dohrn-Strasse 8-10, 10589 Berlin, Germany.
Department of Nutritional Toxicology, German Institute of Human Nutrition (DIfE), Potsdam-Rehbrücke, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany.
Int J Mol Sci. 2024 Mar 29;25(7):3824. doi: 10.3390/ijms25073824.
We previously found that feeding rats with broccoli or cauliflower leads to the formation of characteristic DNA adducts in the liver, intestine and various other tissues. We identified the critical substances in the plants as 1-methoxy-3-indolylmethyl (1-MIM) glucosinolate and its degradation product 1-MIM-OH. DNA adduct formation and the mutagenicity of 1-MIM-OH in cell models were drastically enhanced when human sulfotransferase (SULT) 1A1 was expressed. The aim of this study was to clarify the role of SULT1A1 in DNA adduct formation by 1-MIM-OH in mouse tissues in vivo. Furthermore, we compared the endogenous mouse Sult1a1 and transgenic human SULT1A1 in the activation of 1-MIM-OH using genetically modified mouse strains. We orally treated male wild-type (wt) and Sult1a1-knockout (ko) mice, as well as corresponding lines carrying the human gene cluster (tg and ko-tg), with 1-MIM-OH. -(1-MIM)-dG and -(1-MIM)-dA adducts in DNA were analysed using isotope-dilution UPLC-MS/MS. In the liver, caecum and colon adducts were abundant in mice expressing mouse and/or human SULT1A1, but were drastically reduced in ko mice (1.2-10.6% of wt). In the kidney and small intestine, adduct levels were high in mice carrying human genes, but low in wt and ko mice (1.8-6.3% of tg-ko). In bone marrow, adduct levels were very low, independently of the SULT1A1 status. In the stomach, they were high in all four lines. Thus, adduct formation was primarily controlled by SULT1A1 in five out of seven tissues studied, with a strong impact of differences in the tissue distribution of mouse and human SULT1A1. The behaviour of 1-MIM-OH in these models (levels and tissue distribution of DNA adducts; impact of SULTs) was similar to that of methyleugenol, classified as "probably carcinogenic to humans". Thus, there is a need to test 1-MIM-OH for carcinogenicity in animal models and to study its adduct formation in humans consuming brassicaceous foodstuff.
我们之前发现,给老鼠喂食西兰花或花椰菜会导致其肝脏、肠道和各种其他组织中形成特征性的 DNA 加合物。我们鉴定出植物中的关键物质为 1-甲氧基-3-吲哚甲基(1-MIM)葡萄糖硫苷及其降解产物 1-MIM-OH。当人磺基转移酶(SULT)1A1 表达时,1-MIM-OH 的 DNA 加合物形成和细胞模型中的致突变性大大增强。本研究的目的是阐明 SULT1A1 在体内 1-MIM-OH 形成 DNA 加合物中的作用。此外,我们使用基因修饰的小鼠品系比较了内源性小鼠 Sult1a1 和转基因人 SULT1A1 对 1-MIM-OH 的激活作用。我们用 1-MIM-OH 口服处理雄性野生型(wt)和 Sult1a1 敲除(ko)小鼠,以及携带人基因簇的相应线(tg 和 ko-tg)。使用同位素稀释 UPLC-MS/MS 分析 DNA 中的 -(1-MIM)-dG 和 -(1-MIM)-dA 加合物。在肝脏、盲肠和结肠中,在表达鼠和/或人 SULT1A1 的小鼠中加合物丰富,但在 ko 小鼠中则大大减少(wt 的 1.2-10.6%)。在肾脏和小肠中,在携带人基因的小鼠中加合物水平较高,但在 wt 和 ko 小鼠中较低(tg-ko 的 1.8-6.3%)。在骨髓中,加合物水平非常低,与 SULT1A1 状态无关。在胃中,四条线均高。因此,在研究的七个组织中的五个组织中,加合物形成主要受 SULT1A1 控制,鼠和人 SULT1A1 的组织分布差异有很大影响。1-MIM-OH 在这些模型中的行为(DNA 加合物的水平和组织分布;SULT 的影响)与被归类为“可能对人类致癌”的甲基丁香酚相似。因此,需要在动物模型中测试 1-MIM-OH 的致癌性,并研究人类食用十字花科食物时其加合物的形成。