Radford-Smith Daniel E, Probert Fay, Burnet Philip W J, Anthony Daniel C
Department of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.
Department of Chemistry, University of Oxford, Oxford OX1 3TA, United Kingdom.
Proc Natl Acad Sci U S A. 2022 Mar 1;119(9). doi: 10.1073/pnas.2108581119.
Maternal obesity disturbs brain-gut-microbiota interactions and induces negative affect in the offspring, but its impact on gut and brain metabolism in the offspring (F1) are unknown. Here, we tested whether perinatal intake of a multispecies probiotic could mitigate the abnormal emotional behavior in the juvenile and adult offspring of obese dams. Untargeted NMR-based metabolomic profiling and gene-expression analysis throughout the gut-brain axis were then used to investigate the biology underpinning behavioral changes in the dams and their offspring. Prolonged high-fat diet feeding reduced maternal gut short-chain fatty acid abundance, increased markers of peripheral inflammation, and decreased the abundance of neuroactive metabolites in maternal milk during nursing. Both juvenile (postnatal day [PND] 21) and adult (PND112) offspring of obese dams exhibited increased anxiety-like behavior, which were prevented by perinatal probiotic exposure. Maternal probiotic treatment increased gut butyrate and brain lactate in the juvenile and adult offspring and increased the expression of prefrontal cortex , a marker of glycolytic metabolism in astrocytes. expression correlated with the increase in gut butyrate in the juvenile and adult offspring. Maternal obesity reduced synaptophysin expression in the adult offspring, while perinatal probiotic exposure increased expression of brain-derived neurotrophic factor. Finally, we showed that the resilience of juvenile and adult offspring to anxiety-like behavior was most prominently associated with increased brain lactate abundance, independent of maternal group. Taken together, we show that maternal probiotic supplementation exerts a long-lasting effect on offspring neuroplasticity and the offspring gut-liver-brain metabolome, increasing resilience to emotional dysfunction induced by maternal obesity.
母体肥胖会扰乱脑-肠-微生物群的相互作用,并在后代中诱发负面影响,但其对后代(F1)肠道和大脑代谢的影响尚不清楚。在这里,我们测试了围产期摄入多种益生菌是否可以减轻肥胖母鼠的幼年和成年后代的异常情绪行为。然后,我们使用基于非靶向核磁共振的代谢组学分析和贯穿脑-肠轴的基因表达分析,来研究母鼠及其后代行为变化背后的生物学机制。长期高脂饮食会降低母体肠道短链脂肪酸的丰度,增加外周炎症标志物,并降低哺乳期母鼠乳汁中神经活性代谢物的丰度。肥胖母鼠的幼年(出生后第21天[PND])和成年(PND112)后代均表现出焦虑样行为增加,而围产期暴露于益生菌可预防这种情况。母体益生菌治疗可增加幼年和成年后代肠道中的丁酸盐和大脑中的乳酸盐,并增加前额叶皮层的表达,这是星形胶质细胞糖酵解代谢的标志物。该表达与幼年和成年后代肠道丁酸盐的增加相关。母体肥胖会降低成年后代中突触素的表达,而围产期暴露于益生菌则会增加脑源性神经营养因子的表达。最后,我们表明,幼年和成年后代对焦虑样行为的恢复力最显著地与大脑乳酸盐丰度的增加有关,与母体组无关。综上所述,我们表明母体补充益生菌对后代神经可塑性和后代肠道-肝脏-大脑代谢组具有持久影响,可增强对母体肥胖诱导的情绪功能障碍的恢复力。