Yang Cong, Sun Jingxi, Li Ling, Zheng Jin, Wang Chuhan, Zhao Yu, Yun Duo, Jia Mengzhen, Wu Zhinan, Liang Hewei, Li Wenxi, Hu Tongyuan, Guo Rui, Xiao Liang, Zou Yuanqiang, Liu Zhigang
College of Food Science and Engineering, Northwest A&F University, Yangling, China.
BGI Research, Shenzhen, China.
Alzheimers Dement. 2025 Jul;21(7):e70406. doi: 10.1002/alz.70406.
Recent studies have found that gut microbial tryptophan metabolism is altered in Alzheimer's disease (AD) patients. However, the functional consequences of these changes and their therapeutic potential remain unclear.
The metagenomic data of 49 preclinical AD patients and 115 healthy controls were analyzed. A synbiotic with targeted metabolic functions was formulated based on in vitro testing, and its effect on AD was evaluated using female 5×FAD mice.
Indole lactic acid (ILA) synthesis was downregulated in AD patients. Synbiotic treatment combining Lactobacillus suilingensis and inulin outperformed probiotic treatment alone in enhancing tryptophan metabolism, and increasing ILA biosynthesis. Increased ILA could reduce Aβ accumulation and significantly alleviate cognitive impairment in female AD mice by inhibiting neuroinflammation through activation of the aryl hydrocarbon receptor (AhR) signaling pathway.
This study highlights the therapeutic potential of targeting gut microbial tryptophan metabolism in AD and provides a rationale for future precision strategies aimed at modulating microbiota-derived metabolic pathways.
Gut metagenomic analysis reveals reduced indole lactic acid (ILA) biosynthesis genes in preclinical AD patients. Screening and formulating ILA-producing synbiotic by using whole-genome analysis. Synbiotic treatment alleviates cognitive impairment and promotes ILA synthesis in female 5×FAD mice. ILA alleviates neuroinflammation in female 5×FAD mice by activating aryl hydrocarbon receptor (AhR) in the brain. Synbiotic targeting tryptophan metabolism provides a novel approach for Alzheimer's intervention.
最近的研究发现,阿尔茨海默病(AD)患者的肠道微生物色氨酸代谢发生了改变。然而,这些变化的功能后果及其治疗潜力仍不清楚。
分析了49例临床前AD患者和115例健康对照的宏基因组数据。基于体外测试配制了具有靶向代谢功能的合生元,并使用雌性5×FAD小鼠评估其对AD的影响。
AD患者中吲哚乳酸(ILA)合成下调。在增强色氨酸代谢和增加ILA生物合成方面,将猪源乳酸杆菌和菊粉联合使用的合生元治疗优于单独的益生菌治疗。增加的ILA可以通过激活芳烃受体(AhR)信号通路抑制神经炎症,从而减少Aβ积累并显著减轻雌性AD小鼠的认知障碍。
本研究突出了针对AD中肠道微生物色氨酸代谢的治疗潜力,并为未来旨在调节微生物群衍生代谢途径的精准策略提供了理论依据。
肠道宏基因组分析显示临床前AD患者中吲哚乳酸(ILA)生物合成基因减少。通过全基因组分析筛选和配制产生ILA的合生元。合生元治疗可减轻雌性5×FAD小鼠的认知障碍并促进ILA合成。ILA通过激活大脑中的芳烃受体(AhR)减轻雌性5×FAD小鼠的神经炎症。靶向色氨酸代谢的合生元为阿尔茨海默病的干预提供了一种新方法。