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肠道微生物群代谢物的新兴化学生理多样性。

Emerging chemophysiological diversity of gut microbiota metabolites.

机构信息

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, Zhejiang, China.

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, Zhejiang, China; Jinhua Institute of Zhejiang University, Jinhua 321299, Zhejiang, China; State Key Laboratory of Advanced Drug Delivery and Release Systems, Zhejiang University, Hangzhou 310058, Zhejiang, China.

出版信息

Trends Pharmacol Sci. 2024 Sep;45(9):824-838. doi: 10.1016/j.tips.2024.07.006. Epub 2024 Aug 10.

Abstract

Human physiology is profoundly influenced by the gut microbiota, which generates a wide array of metabolites. These microbiota-derived compounds serve as signaling molecules, interacting with various cellular targets in the gastrointestinal tract and distant organs, thereby impacting our immune, metabolic, and neurobehavioral systems. Recent advancements have unveiled unique physiological functions of diverse metabolites derived from tryptophan (Trp) and bile acids (BAs). This review highlights the emerging chemophysiological diversity of these metabolites and discusses the role of chemical and biological tools in analyzing and therapeutically manipulating microbial metabolism and host targets, with the aim of bridging the chemical diversity with physiological complexity in host-microbe molecular interactions.

摘要

人体生理学深受肠道微生物群的影响,这些微生物群产生了广泛的代谢物。这些源自微生物群的化合物作为信号分子,与胃肠道和远处器官中的各种细胞靶标相互作用,从而影响我们的免疫、代谢和神经行为系统。最近的研究揭示了色氨酸(Trp)和胆汁酸(BAs)衍生的多种代谢物的独特生理功能。本综述强调了这些代谢物化学生理学多样性的出现,并讨论了化学和生物学工具在分析和治疗性操纵微生物代谢和宿主靶标中的作用,旨在将宿主-微生物分子相互作用中的化学多样性与生理复杂性联系起来。

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