Pan Miaomiao, Qian Chenglang, Huo Shaoye, Wu Yuchen, Zhao Xinyi, Ying Yueming, Wang Boyu, Yang Hao, Yeerken Anaguli, Wang Tongyao, Fu Mengwei, Wang Lihong, Wei Yuhuan, Zhao Yunhua, Shao Chunhai, Wang Huijing, Zhao Chao
MOE/NHC/CAMS Key Lab of Medical Molecular Virology, School of Basic Medical Sciences, & National Clinical Research Center for Aging and Medicine, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Department of Clinical Nutrition, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Gut Microbes. 2025 Dec;17(1):2447834. doi: 10.1080/19490976.2024.2447834. Epub 2025 Jan 9.
The gut microbiota plays a pivotal role in anxiety regulation through pathways involving neurotransmitter production, immune signaling, and metabolic interactions. Among these, gut-derived serotonin (5-hydroxytryptamine, 5-HT), synthesized from tryptophan metabolism, has been identified as a key mediator. However, it remains unclear whether specific microbial factors regulate tryptophan metabolism to influence 5-HT production and anxiety regulation. In this study, we analyzed 110 athletes undergoing closed training and found that fecal lactate levels were significantly associated with anxiety indicators. We observed a significant negative correlation between abundance and anxiety levels in athletes. Co-supplementation with lactate and () modulated tryptophan metabolism by increasing key enzyme TPH1 and reducing IDO1, thus shifting metabolism from kynurenine (Kyn) to 5-HT. In addition, lactate enhanced the propionate production capacity of , potentially contributing to anxiety reduction in mice. Taken together, these findings suggest that enteric lactate and collaboratively restore the imbalance in tryptophan metabolism, leading to increased 5-HT activity and alleviating anxiety phenotypes. This study highlights the intricate interplay between gut metabolites and anxiety regulation, offering potential avenues for microbiota-targeted therapeutic strategies for anxiety.
肠道微生物群通过涉及神经递质产生、免疫信号传导和代谢相互作用的途径在焦虑调节中发挥关键作用。其中,由色氨酸代谢合成的肠道源性血清素(5-羟色胺,5-HT)已被确定为关键介质。然而,尚不清楚特定的微生物因素是否调节色氨酸代谢以影响5-HT的产生和焦虑调节。在本研究中,我们分析了110名接受封闭式训练的运动员,发现粪便乳酸水平与焦虑指标显著相关。我们观察到运动员体内丰度与焦虑水平之间存在显著负相关。乳酸与()共同补充通过增加关键酶TPH1和降低IDO1来调节色氨酸代谢,从而使代谢从犬尿氨酸(Kyn)转向5-HT。此外,乳酸增强了的丙酸产生能力,可能有助于减轻小鼠的焦虑。综上所述,这些发现表明肠道乳酸和共同恢复色氨酸代谢的失衡,导致5-HT活性增加并减轻焦虑表型。本研究突出了肠道代谢物与焦虑调节之间的复杂相互作用,为焦虑的微生物群靶向治疗策略提供了潜在途径。