神经炎症
肠道菌群
真细菌
代谢组学
疾病
生物
痴呆
梭菌目
梭菌
医学
生物信息学
免疫学
病理
细菌
遗传学
作者
Huifen Ma,Zhiyang Yu,Qiong Qiao,Wenpan Wang,Zhonghua Li,Pan Wang,Junying Song,Xiaowei Zhang,Yunfang Su,Yiran Sun,Zhishen Xie,Zhenqiang Zhang
出处
期刊:iScience
[Cell Press]
日期:2025-06-03
卷期号:28 (7): 112817-112817
被引量:1
标识
DOI:10.1016/j.isci.2025.112817
摘要
There has been increasing interest in the connection between AD, gut microbiota, and metabolites. Kai-Xin-San (KXS) has been commonly employed in ancient and modern Chinese clinical trials for the treatment of dementia; however, whether the protective effect of KXS in AD is related to the gut microbiota remains elusive. APP/PS1 mice were used as the model of AD. 43 key metabolites influenced by KXS were screened using untargeted metabolomics. At the genus level, Clostridium_IV, Eubacterium, Acetatifactor, etc., were identified to be impacted by KXS using 16S rRNA sequencing. Additionally, we identified 9 distinct intestinal floras at the genus level that were correlated with 13 pivotal differential metabolites related to cognitive impairment. KXS also inhibited the neuroinflammation, mostly via regulating the key metabolites. A potential relationship between gut microbiota, metabolites, and neuroinflammation is suggested as a protective mechanism of KXS in AD. These findings provide support for further development of KXS.
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