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青钱柳叶多糖通过调节短链脂肪酸和肠道微生物组成改善肠道微生物群的代谢功能。

Cyclocarya paliurus polysaccharide improves metabolic function of gut microbiota by regulating short-chain fatty acids and gut microbiota composition.

机构信息

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China.

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China.

出版信息

Food Res Int. 2021 Mar;141:110119. doi: 10.1016/j.foodres.2021.110119. Epub 2021 Jan 11.

Abstract

The purpose of this paper was to investigate the effects of Cyclocarya paliurus polysaccharide (CP) on gut microbiota composition and predict metabolic function in healthy mice. Healthy Kunming mice were continuously gavaged with CP for 20 days, and mouse feces were collected for analysis. The results showed that CP could remarkably increase the short-chain fatty acids (SCFAs; acetic acid, propionic acid, butyric acid, and valeric acid) in the feces of healthy mice in a dose-dependent matter. 16S rRNA showed that 200 mg/kg body weight CP was effective in increasing diversity of the gut microbiota in healthy mice and affected the relative abundance of specific bacteria. Lachnospiraceae, Clostridiales, and Clostridia were identified as the phenotypic biomarkers of the CP-H group compared with the normal control group. In addition, PICRUSt2 showed that starch and sucrose metabolism, amino acid metabolism, glycerolipid metabolism, pantothenate and CoA biosynthesis, biosynthesis of unsaturated fatty acids, and C5-branched dibasic acid metabolism are the primary enriched phenotypic KEGG pathways in the CP-H group. These findings suggested that early CP intervention could enhance the metabolic function of gut microbiota by increasing the release of SCFAs and altering the composition of gut microbiota.

摘要

本文旨在研究青钱柳多糖(CP)对健康小鼠肠道微生物组成的影响,并预测其代谢功能。将健康昆明小鼠连续灌胃 CP 20 天,收集小鼠粪便进行分析。结果表明,CP 可显著增加健康小鼠粪便中短链脂肪酸(SCFAs;乙酸、丙酸、丁酸和戊酸)的含量,呈剂量依赖性。16S rRNA 显示,200mg/kg 体重 CP 可有效增加健康小鼠肠道微生物群的多样性,并影响特定细菌的相对丰度。与正常对照组相比,lachnospiraceae、Clostridiales 和 Clostridia 被鉴定为 CP-H 组的表型生物标志物。此外,PICRUSt2 显示,淀粉和蔗糖代谢、氨基酸代谢、甘油脂质代谢、泛酸和辅酶 A 生物合成、不饱和脂肪酸生物合成和 C5-支链二羧酸代谢是 CP-H 组中主要富集的表型 KEGG 途径。这些发现表明,早期 CP 干预可以通过增加 SCFAs 的释放和改变肠道微生物群的组成来增强肠道微生物群的代谢功能。

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