Sennoside A alleviating cognitive impairment in APP/PS1 mice via balancing microbiome metabolism

肠道菌群 失调 肠-脑轴 粪便细菌疗法 医学 微生物群 神经炎症 认知 疾病 病态的 代谢组学 机制(生物学) 生物 代谢途径 生物信息学 粪便 肠道微生物群 肠易激综合征 神经化学 帕金森病 治疗方法 治疗效果 认知功能衰退 免疫学 新陈代谢 神经科学 生理学
作者
Yulian Shi,HaiRong Ma,Huajinzi Li,Yingyue Wang,Chaofan Wang,Nengchong Zhang,Gan Luo,Ying Wang,Xiaoyan Gao
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:108 (4): 1659-1676 被引量:1
标识
DOI:10.1177/13872877251389922
摘要

Background The progression of Alzheimer's disease (AD) is associated with constipation, potentially mediated by gut microbiota. Laxatives have shown potential in improving the cognitive function of AD, but the specific mechanism remains underexplored. Sennoside A (SA), a well-established laxative, is commonly used for treating constipation. Objective This work used SA as a probe to explore the therapeutic effects and potential mechanisms of laxatives on AD via the gut-brain axis. Methods Following a two-month treatment, behavioral experiments were used to assess the cognitive function. The central pathologies and neuroinflammation were evaluated by histopathology and ELISA. 16S rRNA sequencing, fecal microbiota transplantation and antibiotic treatment were conducted to verify whether SA exerts anti-AD effects via gut microbiota. Further, non-targeted metabolomics coupled with Spearman correlation analysis was employed to elucidate the underlying mechanisms. Results SA significantly countered cognitive dysfunction and central pathological damage in APP/PS1 mice. Besides, SA ameliorated gut dysbiosis and affected the metabolic functions of the flora. Furthermore, the therapeutic effects of SA decrease with the depletion of gut microbes and could be transferred with the microbiota. Intriguingly, amino acid metabolism and aminoacyl-tRNA biosynthesis were the main metabolic pathways regulated by SA, consistent with the predicted functions of gut bacteria. Finally, correlation analysis revealed a strong correlation between gut microbes, fecal metabolites, and cognitive ability affected by SA. Conclusions The study investigated the efficacy and mechanisms of laxatives represented by SA for AD from the perspective of the gut-brain axis.
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