Department of Epigenetic Epidemiology/Molecular Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.
Animal Research Center, Tokyo Medical University, 6-1-1, Shinjyuku, Shinjyuku-ku, Tokyo, 160-0022, Japan.
Sci Rep. 2017 Aug 29;7(1):9812. doi: 10.1038/s41598-017-10380-4.
Maternal low-protein (MLP) diet can lead to hepatic steatosis, which only develops with ageing. It is still unclear whether the young offspring show any signs of past exposure to prenatal adverse conditions. We hypothesized that early nutritional insult would first affect the dynamic responsiveness to nutritional challenges rather than the static state. We analyzed the transcriptome and metabolome profiles of the hepatic response to fasting/refeeding in young male mice offspring to identify changes induced by early gestational MLP diet. Restricted MLP exposure strictly to early gestation was achieved by the embryo transfer method. As a result, the fasting-induced upregulation of genes related to long-chain fatty acid metabolism and of stress response genes related to protein folding were significantly diminished in MLP pups. Lipid profiling after fasting showed that the hepatic signature of triacylglycerols was shifted to longer acyl-chains and higher saturation by the MLP diet. Bioinformatic analyses suggested that these phenomenological changes may be partially linked to the peroxisome proliferator activated receptor α (PPARα) pathway. Taken together, early gestational MLP diet affected the hepatic dynamic response to nutritional stress in seemingly healthy young offspring, accompanied with partial deterioration of PPARα action.
母体低蛋白(MLP)饮食可导致肝脂肪变性,且仅在衰老时发生。目前尚不清楚年轻后代是否有过去暴露于产前不良环境的迹象。我们假设早期营养损伤首先会影响对营养挑战的动态反应能力,而不是静态状态。我们分析了年轻雄性小鼠后代肝脏对禁食/再喂养反应的转录组和代谢组谱,以鉴定早期妊娠 MLP 饮食诱导的变化。通过胚胎移植方法严格限制 MLP 仅在早期妊娠暴露。结果,MLP 幼鼠中与长链脂肪酸代谢相关的基因以及与蛋白质折叠相关的应激反应基因的禁食诱导上调显著减少。禁食后的脂质分析表明,MLP 饮食使肝脏三酰甘油的特征向更长的酰链和更高的饱和度转移。生物信息学分析表明,这些现象学变化可能部分与过氧化物酶体增殖物激活受体α(PPARα)途径有关。总之,早期妊娠 MLP 饮食影响了看似健康的年轻后代对营养应激的肝脏动态反应能力,同时伴有 PPARα 作用的部分恶化。