非诺贝特能改善高脂饮食仓鼠肠道微生物群的组成和代谢途径

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Qifeng Liu
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引用次数: 0

摘要

非诺贝特是一种具有多种生物特性的化合物,可用于降低血脂。了解肠道微生物群对高脂血症的影响对于控制全身炎症和改善血清脂质控制至关重要。然而,非诺贝特对常驻肠道细菌表型和基因表达的具体影响,以及对微生物代谢转化为功能网络的影响仍不清楚。在本研究中,我们的目的是研究喂食高脂饮食(HFD)并服用非诺贝特的仓鼠肠道微生物群的基因和代谢途径。在这项研究中,我们对使用非诺贝特治疗的高脂饮食仓鼠样本进行了元基因组分析。结果表明,非诺贝特能显著降低高脂血症仓鼠的血清脂质水平。与高脂血症仓鼠组相比,使用非诺贝特治疗的仓鼠组表现出更高水平的与健康相关的有益细菌,包括卵形乳杆菌(Bacteroides ovatus)、动物双歧杆菌(Bifidobacterium animalis)、肠道乳杆菌(Bacteroides intestinalis)、嗜盐乳杆菌(Allobaculum stercoricanis)、纽特乳杆菌(Lactobacillus reuteri)和酸性乳杆菌(Bacteroides acidifaciens)。此外,代谢途径分析表明,膳食非诺贝特能显著促进不饱和脂肪酸的生物合成、甘油磷脂代谢和嘧啶代谢,同时降低乙醛酸盐和二羧酸盐代谢、酪氨酸代谢、色氨酸代谢和非核糖体肽结构。此外,这些代谢途径的变化与京都基因和基因组百科全书(KEGG)数据库中基因丰度的相对变化有关,即 K01667、K11358、K13953、K04072、K06131、K00655、K04567、K02864、K06409、K05366、K01867、K21071 和 K13292。此外,还观察到与碳水化合物和抗生素抗性有关的重要变化,如糖基转移酶家族 51(GT51)以及 adeC、carA 和 MexT。膳食非诺贝特对肠道菌群以及与脂质、能量和氨基酸代谢相关的基因有显著影响,最终促进宿主获得更健康的结肠环境。这些发现有助于更好地理解非诺贝特的作用机制,并为未来的实验和临床研究提供了宝贵的基础,旨在探索其实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fenofibrate alleviates the composition and metabolic pathways of gut microbiota in high-fat diet treated hamsters
Fenofibrate is a compound with diverse biological properties that can be utilized to lower blood lipids. Understanding the impact of the gut microbiota in hyperlipidemia is vital for controlling systemic inflammation and improving serum lipid control. Nevertheless, the specific effects of fenofibrate on the phenotype and gene expression of resident gut bacteria, as well as its influence on the transformation of microbial metabolism into functional networks, remain unclear. In this study, our aimed to examine the gene and metabolic pathways of the gut microbiota in a hamster fed a high-fat diet (HFD) and administered fenofibrate. In this study, we conducted metagenomic analyses on samples from HFD hamsters treated with fenofibrate. The results indicated that fenofibrate treatments significantly reduce the serum lipid levels in hyperlipidemia hamsters. And the group treated with fenofibrate exhibited higher levels of beneficial bacterial species associated with health, including Bacteroides ovatus, Bifidobacterium animalis, Bacteroides intestinalis, Allobaculum stercoricanis, Lactobacillus reuteri, and Bacteroides acidifaciens, in comparison to the HFD group. Additionally, analysis of metabolic pathways demonstrated that dietary fenofibrate significantly enhanced the biosynthesis of unsaturated fatty acids, glycerophospholipid metabolism, and pyrimidine metabolism, while reducing glyoxylate and dicarboxylate metabolism, tyrosine metabolism, tryptophan metabolism, and nonribosomal peptide structures. Furthermore, these metabolic pathway changes were associated with relative alterations in the abundance of genes from the Kyoto Encyclopedia of Genes and Genomes (KEGG) database, namely K01667, K11358, K13953, K04072, K06131, K00655, K04567, K02864, K06409, K05366, K01867, K21071, and K13292. Moreover, significant changes were observed in related to carbohydrate and antibiotic resistance, such as glycosyltransferase family 51 (GT51) as well as adeC, carA, and MexT. Dietary fenofibrate exerted significant effects on intestinal flora and genes related to lipid, energy, and amino acid metabolism, ultimately promoting a healthier colonic environment for the host. And these findings contribute to a better understanding of the mechanism of action of fenofibrate and provide a valuable foundation for future experimental and clinical studies, aiming to explore its practical applications.
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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