神经炎症
芳香烃受体
化学
芳基
小胶质细胞
代谢物
碳氢化合物
受体
生物化学
药理学
炎症
生物
医学
内科学
有机化学
基因
转录因子
烷基
作者
Jing Sun,Yuhe Zhang,Yu Kong,Tao Ye,Qingxia Yu,Senthil Kumaran Satyanarayanan,Kuan‐Pin Su,Jiaming Liu
标识
DOI:10.1016/j.bbi.2022.08.003
摘要
Gut microbiota alterations might affect the development of Alzheimer's disease (AD) through microbiota-derived metabolites. For example, microbiota-derived Indoles via tryptophan metabolism prevented Aβ accumulation and Tau hyperphosphorylation, restored synaptic plasticity, and then promoted the cognitive and behavioral ability of APP/PS1 mice. The imbalanced compositions of Indoles-producing bacteria with tryptophan deficiency were found in male APP/PS1 mice, but the molecular mechanisms remained unclear. Our current study revealed that Indoles (including indole, indole-3-acetic acid and indole-3-propionic acid) upregulated the production of aryl hydrocarbon receptor (AhR), inhibited the activation of the NF-κB signal pathway as well as the formation of the NLRP3 inflammasome, reduced the release of inflammatory cytokines, including TNF-α, IL-6, IL-1β and IL-18, alleviating the inflammatory response of APP/PS1 mice. These findings demonstrated the roles of Indoles-producing bacteria in activating the AhR pathway to regulate neuroinflammation of AD through gut microbiota-derived Indoles, which implied a novel way for AD treatment.
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