Laboratoire PériTox-INERIS UMR_I 01, Université Picardie Jules Verne, Amiens, France; Institut Polytechnique UniLaSalle, Université d'Artois, ULR 7519, Beauvais, France.
Laboratoire PériTox-INERIS UMR_I 01, Université Picardie Jules Verne, Amiens, France.
Cells Dev. 2021 Jun;166:203678. doi: 10.1016/j.cdev.2021.203678. Epub 2021 Apr 19.
Metabolic impairments in childhood are known to promote the development of type 2 diabetes and/or obesity in adulthood. These impairments may result from perinatal exposure to harmful environmental factors, such as pesticide residues or the consumption of a "western" diet. In the present study, we sought to determine whether an obesogenic profile, metabolic disorders and liver damage in offspring (observed during young adulthood) were related to maternal exposure to the pesticide chlorpyrifos (CPF) and/or a high-fat diet (HFD) starting 4 months before conception and ending at weaning. After the end of exposure, 51 male rat pups were left to develop under normal conditions and were studied in young adulthood. Despite the absence of direct exposure to harmful factors (other than through the dam's milk), maternal exposure to CPF or an HFD was associated with changes in the offspring's metabolic activity in the liver in the offspring. This indirect exposure to CPF was associated with a relative reduction in the expression of genes coding for enzymes involved in lipid or glucose metabolism but did induce histopathological changes in the offspring at adulthood. Maternal exposure to an HFD alone or to CPF alone gave similar results in offspring, changes in the same direction. Exposure of the mother to HFD did not exacerbate CPF effects. Co-exposure to both CPF and HFD did not increase the observed effects compared to each factor taken separately.
已知儿童时期的代谢损伤会促进成年后患 2 型糖尿病和/或肥胖。这些损伤可能是由于围产期接触有害环境因素引起的,如农药残留或“西式”饮食。在本研究中,我们试图确定肥胖相关表型、后代(在青年期观察到)的代谢紊乱和肝损伤是否与母体在受孕前 4 个月开始至断奶结束时接触杀虫剂毒死蜱(CPF)和/或高脂肪饮食(HFD)有关。暴露结束后,51 只雄性幼鼠在正常条件下发育,并在青年期进行研究。尽管没有直接接触有害因素(除了通过母鼠的乳汁),但母体接触 CPF 或 HFD 与后代肝脏代谢活性的变化有关。这种间接接触 CPF 与参与脂质或葡萄糖代谢的酶的编码基因的表达相对减少有关,但在成年时确实会诱导后代发生组织病理学变化。母体单独接触 HFD 或 CPF 会在后代中产生类似的结果,变化方向相同。母体暴露于 HFD 不会加剧 CPF 的作用。与单独接触 CPF 或 HFD 相比,同时接触两者并没有增加观察到的效果。