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Age-related shifts in gut microbiota contribute to cognitive decline in aged rats

机译:年龄相关的肠道菌群变化导致老年大鼠认知能力下降

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摘要

Cognitive function declines during the aging process, meanwhile, gut microbiota of the elderly changed significantly. Although previous studies have reported the effect of gut microbiota on learning and memory, all the reports were based on various artificial interventions to change the gut microbiota without involvement of aging biological characteristics. Here, we investigated the effect of aged gut microbiota on cognitive function by using fecal microbiota transplantation (FMT) from aged to young rats. Results showed that FMT impaired cognitive behavior in young recipient rats; decreased the regional homogeneity in medial prefrontal cortex and hippocampus; changed synaptic structures and decreased dendritic spines; reduced expression of brain-derived neurotrophic factor (BDNF), N-methyl-D-aspartate receptor NR1 subunit, and synaptophysin; increased expression of advanced glycation end products (AGEs) and receptor for AGEs (RAGE). All these behavioral, brain structural and functional alterations induced by FMT reflected cognitive decline. In addition, FMT increased levels of pro-inflammatory cytokines and oxidative stress in young rats, indicating that inflammation and oxidative stress may underlie gut-related cognitive decline in aging. This study provides direct evidence for the contribution of gut microbiota to the cognitive decline during normal aging and suggests that restoring microbiota homeostasis in the elderly may improve cognitive function.
机译:衰老过程中认知功能下降,同时老年人肠道菌群发生明显变化。尽管以前的研究已经报道了肠道菌群对学习和记忆的影响,但是所有报告都是基于各种人工干预来改变肠道菌群而没有老化生物特征的。在这里,我们通过使用从老年到幼年大鼠的粪便微生物菌群移植(FMT),研究了老年肠道菌群对认知功能的影响。结果表明,FMT损害了幼鼠的认知行为。降低内侧前额叶皮层和海马的区域同质性;改变突触结构并减少树突棘;降低脑源性神经营养因子(BDNF),N-甲基-D-天冬氨酸受体NR1亚基和突触素的表达;晚期糖基化终产物(AGEs)和AGEs受体(RAGE)的表达增加。 FMT引起的所有这些行为,大脑结构和功能改变均反映了认知能力下降。此外,FMT增加了幼鼠促炎性细胞因子和氧化应激的水平,表明炎症和氧化应激可能是与肠道相关的衰老认知下降的基础。这项研究提供了正常衰老过程中肠道菌群对认知能力下降的贡献的直接证据,并表明恢复老年人的菌群稳态可以改善认知功能。

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