Høie Anja Hortemo, Monien Bernhard Hans, Glatt Hansruedi, Hjertholm Hege, Husøy Trine
Department of Food, Water and Cosmetics, Division of Environmental Medicine, Norwegian Institute of Public Health, 0456 Oslo, Norway.
Research Group Genotoxic Food Contaminants, Department of Nutritional Toxicology, German Institute of Human Nutrition Potsdam-Rehbrücke, 14558 Nuthetal, Germany; Department of Food Safety, Federal Institute for Risk Assessment, 10589 Berlin, Germany.
Toxicol Lett. 2016 Apr 25;248:34-8. doi: 10.1016/j.toxlet.2016.02.017. Epub 2016 Mar 3.
Food processing contaminant 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) has previously been shown to induce formation of DNA adducts in vivo. In a previous study the adduct levels were found to increase in a mouse model expressing human (h) sulfotransferases (SULTs) 1A1 and 1A2 after PhIP exposure, detected by (32)P-postlabelling. Isotope dilution ultra performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) is emerging as the method of choice for selective and reproducible detection of known DNA adducts. In the present study we investigated the level and distribution of PhIP induced DNA adducts in male FVB mice 9-11 weeks of age with hSULT mice or wild-type mice (wt) using UPLC-MS/MS. Mice received a single administration of 75 mg/kg bw PhIP by oral gavage, and DNA was analysed 3h after exposure. C8-(2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine- N(2)-yl)-2'-deoxyguanosine (C8-PhIP-dG) adduct levels are significantly higher in PhIP exposed hSULT mice compared with PhIP exposed wt mice. The liver was the least affected organ in wild-type mice, whereas it was the most affected organ in hSULT mice with a 14-fold higher adduct level.
食品加工污染物2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)此前已被证明可在体内诱导DNA加合物的形成。在之前的一项研究中,通过³²P后标记法检测发现,在暴露于PhIP后,表达人(h)磺基转移酶(SULTs)1A1和1A2的小鼠模型中加合物水平升高。同位素稀释超高效液相色谱联用串联质谱法(UPLC-MS/MS)正逐渐成为选择性和可重复性检测已知DNA加合物的首选方法。在本研究中,我们使用UPLC-MS/MS研究了9至11周龄的雄性FVB-hSULT小鼠或野生型小鼠(wt)中PhIP诱导的DNA加合物的水平和分布。小鼠通过口服灌胃单次给予75 mg/kg体重的PhIP,并在暴露后3小时分析DNA。与暴露于PhIP的野生型小鼠相比,暴露于PhIP的hSULT小鼠中C8-(2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶-N(2)-基)-2'-脱氧鸟苷(C8-PhIP-dG)加合物水平显著更高。肝脏是野生型小鼠中受影响最小的器官,而在hSULT小鼠中是受影响最大的器官,加合物水平高14倍。