Department of Chemistry, University of California Davis, Davis, California 95616, United States.
School of Veterinary Medicine, University of California Davis, Davis, California 95616, United States.
Anal Chem. 2024 Feb 13;96(6):2415-2424. doi: 10.1021/acs.analchem.3c04352. Epub 2024 Jan 30.
Short-chain fatty acids (SCFAs) comprise the largest group of gut microbial fermentation products. While absorption of most nutrients occurs in the small intestine, indigestible dietary components, such as fiber, reach the colon and are processed by the gut microbiome to produce a wide array of metabolites that influence host physiology. Numerous studies have implicated SCFAs as key modulators of host health, such as in regulating irritable bowel syndrome (IBS). However, robust methods are still required for their detection and quantitation to meet the demands of biological studies probing the complex interplay of the gut-host-health paradigm. In this study, a sensitive, rapid-throughput, and readily expandible UHPLC-QqQ-MS platform using 2-PA derivatization was developed for the quantitation of gut-microbially derived SCFAs, related metabolites, and isotopically labeled homologues. The utility of this platform was then demonstrated by investigating the production of SCFAs in cecal contents from mice feeding studies, human fecal bioreactors, and fecal/bacterial fermentations of isotopically labeled dietary carbohydrates. Overall, the workflow proposed in this study serves as an invaluable tool for the rapidly expanding gut-microbiome and precision nutrition research field.
短链脂肪酸 (SCFAs) 是肠道微生物发酵产物中最大的一类。虽然大多数营养物质的吸收发生在小肠中,但不可消化的膳食纤维等成分会到达结肠,并被肠道微生物群处理,产生广泛的代谢物,影响宿主的生理机能。许多研究表明,SCFAs 是宿主健康的关键调节剂,例如在调节肠易激综合征 (IBS) 方面。然而,为了满足研究肠道-宿主-健康复杂相互作用的生物学研究的需求,仍然需要更灵敏、高通量和易于扩展的检测和定量方法来检测和定量 SCFAs。在这项研究中,我们开发了一种基于 2-PA 衍生化的灵敏、快速、高通量的 UHPLC-QqQ-MS 平台,用于定量检测肠道微生物衍生的 SCFAs、相关代谢物和同位素标记的同源物。然后,通过研究喂食研究、人体粪便生物反应器以及同位素标记膳食碳水化合物的粪便/细菌发酵中盲肠内容物中 SCFAs 的产生,证明了该平台的实用性。总的来说,本研究提出的工作流程为快速发展的肠道微生物组和精准营养研究领域提供了一个非常有价值的工具。