虫草素和冬虫夏草水提取物通过调节肠道微生物群和恢复代谢状况改善小鼠的高尿酸血症

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
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引用次数: 0

摘要

在这项研究中,我们首先筛选并评估了七种药用真菌对高尿酸血症(HUA)等疾病的抑制作用。然后,利用代谢组学和肠道微生物组学方法,重点分析和评估了冬虫夏草水提取物(CME)和虫草素对羟嗪酸钾诱导的高尿酸血症小鼠的影响。研究发现,冬虫夏草水提取物在体内和体外实验中都具有良好的降尿酸活性。它可以通过抑制黄嘌呤氧化酶的活性、减少黄嘌呤前体的产生和抑制胰岛素抵抗来缓解高尿酸血症。虫草素在体内的降尿酸功效与 CME 相当。经CME和虫草素治疗后,Oscillibacter、Alistipes、Prevotellaaceae_NK3B31、Lachnospiraceae_NK4A136的物种丰度下降。盲肠内容物和粪便样本的代谢组学分析从不同角度阐明了CME对高尿酸血症的干预机制。这提示我们在选择样本时应慎重考虑。目前的研究为军事医学研究和维护人类健康提供了科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amelioration of hyperuricemia by cordycepin and Cordyceps militaris aqueous extract in mice via modulating gut microbiota and restoring metabolic profile

In this study, we first screened and evaluated the inhibitory effects of seven medicinal fungi on diseases such as hyperuricemia (HUA). Then, using metabolomics and gut microbiome methods, the focus was on analyzing and evaluating the effects of the aqueous extract of Cordyceps. militaris (CME) and cordycepin on potassium oxyzinate induced HUA mice. It was found that CME exhibits good uric acid lowering activity in both in vivo and in vitro experiments. It can relieve hyperuricemia by inhibiting xanthine oxidase enzyme activity, reducing the production of xanthine precursors, and inhibiting insulin resistance. The uric acid-lowering efficacy of cordycepin in vivo is comparable to that of CME. The species abundance of Oscillibacter, Alistipes, Prevotellaaceae_NK3B31, Lachnospiraceae_NK4A136 were decreased after treatment with CME and cordycepin. The metabolomics analysis of cecal contents and fecal samples elucidated the mechanism of intervention of CME on hyperuricemia from different perspectives. This suggests that we should consider carefully when selecting samples. This current research provides the scientific foundation for the medicinal research of C. militaris and the maintenance of human health.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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