Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China; Canada - China -New Zealand Joint Laboratory of Maternal and Fetal Medicine, Chongqing Medical University, Chongqing 400016, People's Republic of China; Department of Obstetrics and Gynecology, Xin Qiao Hospital, The Second Medical College of Army Medical University, Chongqing, China.
Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China; Canada - China -New Zealand Joint Laboratory of Maternal and Fetal Medicine, Chongqing Medical University, Chongqing 400016, People's Republic of China; Liggins Institute, University of Auckland, Auckland, New Zealand.
Exp Cell Res. 2018 Jul 15;368(2):159-166. doi: 10.1016/j.yexcr.2018.04.019. Epub 2018 Apr 23.
Cognitive impairment is a brain dysfunction characterized by neuropsychological deficits in attention, working memory, and executive function. Maternal obesity and consumption of a high-fat diet (HFD) in the offspring has been suggested to have detrimental consequences for offspring cognitive function through its effect on the hippocampus and prefrontal cortex. Therefore, our study aimed to investigate the effects of maternal obesity and offspring HFD exposure on the brain metabolome of the offspring.
In our pilot study, a LepRdb/+ mouse model was used to model pre-pregnancy maternal obesity and the c57bl/6 wildtype was used as a control group. Offspring were fed either a HFD or a low-fat control diet (LFD) after weaning (between 8 and 10 weeks). The Mirrors water maze was performed between 28 and 30 weeks to measure cognitive function. Fatty acid metabolomic profiles of the prefrontal cortex and hippocampus from the offspring at 30-32 weeks were analyzed using gas chromatography-mass spectrometry.
The memory of male offspring from obese maternal mice, consuming a HFD post-weaning, was significantly impaired when compared to the control offspring mice. No significant differences were observed in female offspring. In male mice, the fatty acid metabolites in the prefrontal cortex were most affected by maternal obesity, whereas, the fatty acid metabolites in the hippocampus were most affected by the offspring's diet. Hexadecanoic acid and octadecanoic acid were significantly affected in both the hippocampus and pre-frontal cortex, as a result of maternal obesity and a HFD in the offspring.
Our findings suggest that the combination of maternal obesity and HFD in the offspring can result in spatial cognitive deficiency in the male offspring, by influencing the fatty acid metabolite profiles in the prefrontal cortex and hippocampus. Further research is needed to validate the results of our pilot study.
认知障碍是一种以注意力、工作记忆和执行功能等神经心理缺陷为特征的大脑功能障碍。母体肥胖和后代高脂肪饮食(HFD)的摄入已被认为通过对海马体和前额叶皮层的影响对后代的认知功能产生不利影响。因此,我们的研究旨在探讨母体肥胖和后代 HFD 暴露对后代大脑代谢组的影响。
在我们的初步研究中,使用 LepRdb/+ 小鼠模型来模拟妊娠前母体肥胖,并用 c57bl/6 野生型作为对照组。后代在断奶后(8-10 周之间)分别喂食 HFD 或低脂对照饮食(LFD)。在 28 至 30 周之间进行 Mirrors 水迷宫实验以测量认知功能。在 30-32 周时,使用气相色谱-质谱法分析后代前额叶皮层和海马体的脂肪酸代谢组谱。
与对照后代相比,从肥胖母体母鼠中喂养 HFD 的雄性后代的记忆明显受损。在雌性后代中未观察到显著差异。在雄性小鼠中,母体肥胖对前额叶皮层的脂肪酸代谢物影响最大,而后代饮食对海马体的脂肪酸代谢物影响最大。十六烷酸和十八烷酸在前额叶皮层和海马体中均受到母体肥胖和后代 HFD 的显著影响。
我们的研究结果表明,母体肥胖和后代 HFD 的结合会导致雄性后代出现空间认知缺陷,这是通过影响前额叶皮层和海马体中的脂肪酸代谢物谱而产生的。需要进一步的研究来验证我们的初步研究结果。