Laboratoire de Biochimie et Nutrition Humaine, INRA USC 1378, Agrocampus Ouest, Rennes, France.
Institut NuMeCan INRA, INSERM, Univ Rennes, Rennes, France.
J Nutr Biochem. 2020 Jan;75:108241. doi: 10.1016/j.jnutbio.2019.108241. Epub 2019 Oct 26.
Non-alcoholic fatty liver disease (NAFLD) has been described as a hepatic manifestation of the metabolic syndrome. When several studies correlated maternal linoleic acid (LA) intake with the development of obesity, only few links have been made between n-6 fatty acid (FA) and NAFLD. Herein, we investigated the influence of both maternal and weaning high LA intake on lipid metabolism and susceptibility to develop later metabolic diseases in offspring. Pregnant rats were fed a control-diet (2% LA) or a LA-rich diet (12% LA) during gestation and lactation. At weaning, offspring was assigned to one of the two diets, i.e., either maintained on the same maternal diet or fed the other diet for 6 months. Physiological, biochemical parameters and hepatic FA metabolism were analyzed. We demonstrated that the interaction between the maternal and weaning LA intake altered metabolism in offspring and could lead to hepatic steatosis. This phenotype was associated with altered hepatic FA content and lipid metabolism. Interaction between maternal and weaning LA intake led to a specific pattern of n-6 and n-3 oxylipins that could participate to the development of hepatic steatosis in offspring. Our findings highlight the significant interaction between maternal and weaning high LA intake to predispose offspring to later metabolic disease and support the predictive adaptive response hypothesis.
非酒精性脂肪性肝病 (NAFLD) 被描述为代谢综合征的肝脏表现。当几项研究将母体亚油酸 (LA) 的摄入量与肥胖的发展相关联时,只有少数 n-6 脂肪酸 (FA) 与 NAFLD 之间存在联系。在此,我们研究了母体和断奶期高 LA 摄入对后代脂质代谢和易患后期代谢性疾病的影响。在妊娠和哺乳期,怀孕的大鼠分别喂食对照饮食(2%LA)或富含 LA 的饮食(12%LA)。在断奶时,后代被分配到两种饮食中的一种,即继续喂食相同的母体饮食或喂食另一种饮食 6 个月。分析生理、生化参数和肝脏 FA 代谢。我们证明,母体和断奶期 LA 摄入的相互作用改变了后代的代谢,可能导致肝脂肪变性。这种表型与肝 FA 含量和脂质代谢的改变有关。母体和断奶期 LA 摄入的相互作用导致特定的 n-6 和 n-3 氧化脂类,这可能参与后代肝脂肪变性的发展。我们的研究结果强调了母体和断奶期高 LA 摄入之间的显著相互作用,使后代易患后期代谢性疾病,并支持预测性适应反应假说。