Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Department of Pediatric Gastroenterology, Emma Children's Hospital Amsterdam, The Netherlands.
Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam The Netherlands.
Curr Opin Clin Nutr Metab Care. 2024 May 1;27(3):297-303. doi: 10.1097/MCO.0000000000001028. Epub 2024 Mar 12.
Emerging evidence suggests that the gut microbiota and its metabolites regulate neurodevelopment and cognitive functioning via a bi-directional communication system known as the microbiota-gut-brain axis (MGBA).
The MGBA influences brain development and function via the hypothalamic-pituitary axis, the vagal nerve, immune signaling, bacterial production of neurotransmitters, and microbial metabolites like short-chain fatty acids, tryptophan derivatives, and bile acids. Animal studies show fetal neurodevelopment is mediated by maternal microbiota derivatives, immune activation, and diet. Furthermore, manipulation of the microbiota during critical windows of development, like antibiotic exposure and fecal microbiota transplantation, can affect cognitive functioning and behavior in mice. Evidence from human studies, particularly in preterm infants, also suggests that a disrupted gut microbiota colonization may negatively affect neurodevelopment. Early microbial signatures were linked to favorable and adverse neurodevelopmental outcomes.
The link between the gut microbiota and the brain is evident. Future studies, including experimental studies, larger participant cohort studies with longitudinal analyses of microbes, their metabolites, and neurotransmitters, and randomized controlled trials are warranted to further elucidate the mechanisms of the MGBA. Identification of early, predictive microbial markers could pave the way for the development of novel early microbiota-based intervention strategies, such as targeted probiotics, and vaginal or fecal microbiota transplantation, aimed at improving infant neurodevelopment.
新出现的证据表明,肠道微生物群及其代谢物通过一种被称为微生物群-肠-脑轴(MGBA)的双向通讯系统来调节神经发育和认知功能。
MGBA 通过下丘脑-垂体轴、迷走神经、免疫信号、细菌产生神经递质以及微生物代谢物(如短链脂肪酸、色氨酸衍生物和胆汁酸)来影响大脑发育和功能。动物研究表明,胎儿神经发育受母体微生物群衍生物、免疫激活和饮食的影响。此外,在发育的关键窗口期(如抗生素暴露和粪便微生物群移植)对微生物群进行操作,可影响小鼠的认知功能和行为。来自人类研究的证据,特别是在早产儿中,也表明肠道微生物群定植的破坏可能对神经发育产生负面影响。早期微生物特征与有利和不利的神经发育结局有关。
肠道微生物群与大脑之间的联系是明显的。需要进一步的研究,包括实验研究、更大的参与者队列研究,对微生物及其代谢物和神经递质进行纵向分析,以及随机对照试验,以进一步阐明 MGBA 的机制。识别早期的、有预测性的微生物标志物可能为开发新的基于早期微生物群的干预策略铺平道路,例如靶向益生菌、阴道或粪便微生物群移植,以改善婴儿的神经发育。