Liupao Tea Ameliorates High-Fat Diet-Induced Non-Alcoholic Fatty Liver Disease via Arginine Metabolism: Insights From Metabolomics and Network Pharmacology

IF 1.8 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Shuyun Wei, Shuiping Zhang, Jiahui Luo, Wenxin Yu, Xing Zeng, Lunli Lan, Cuiping Yu, Yu Zeng, Yi Feng
{"title":"Liupao Tea Ameliorates High-Fat Diet-Induced Non-Alcoholic Fatty Liver Disease via Arginine Metabolism: Insights From Metabolomics and Network Pharmacology","authors":"Shuyun Wei,&nbsp;Shuiping Zhang,&nbsp;Jiahui Luo,&nbsp;Wenxin Yu,&nbsp;Xing Zeng,&nbsp;Lunli Lan,&nbsp;Cuiping Yu,&nbsp;Yu Zeng,&nbsp;Yi Feng","doi":"10.1002/bmc.70166","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Non-alcoholic fatty liver disease (NAFLD) has become a prominent public health concern, closely linked to metabolic syndromes. Liupao tea (LT), a traditional Chinese dark tea, has demonstrated hepatoprotective effects by regulating metabolism. This study investigated the protective effects of LT on HFD-induced NAFLD using metabolomics and network pharmacology approaches. We found that LT significantly reduced energy intake in HFD-fed rats, attenuated abnormal visceral fat accumulation, and prevented hyperlipidemia, abnormal liver lipid deposition, and liver steatosis. Serum untargeted metabolomic analysis identified 46 differential metabolites as potential biomarkers associated with 10 metabolic pathways, including arginine and proline metabolism. Network pharmacology suggested that LT exerts its hepatoprotective effects by regulating arginine metabolism and inflammatory factors; key components, such as caffeine and epigallocatechin gallate, showed direct relevance to NAFLD. Following the intervention, targeted metabolomic analysis revealed a significant change in the levels of 18 relevant amino acids, confirming LT's impact on arginine metabolism. Immunohistochemical results demonstrated reduced expression of inflammatory factors (TNF-α, IL-6, IL-1β) in the liver, suggesting improved liver health. Collectively, these findings indicate that LT mitigates HFD-induced NAFLD through regulation of amino acid metabolism and reduction of inflammatory factors, thereby alleviating liver injury.</p>\n </div>","PeriodicalId":8861,"journal":{"name":"Biomedical Chromatography","volume":"39 9","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedical Chromatography","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bmc.70166","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Non-alcoholic fatty liver disease (NAFLD) has become a prominent public health concern, closely linked to metabolic syndromes. Liupao tea (LT), a traditional Chinese dark tea, has demonstrated hepatoprotective effects by regulating metabolism. This study investigated the protective effects of LT on HFD-induced NAFLD using metabolomics and network pharmacology approaches. We found that LT significantly reduced energy intake in HFD-fed rats, attenuated abnormal visceral fat accumulation, and prevented hyperlipidemia, abnormal liver lipid deposition, and liver steatosis. Serum untargeted metabolomic analysis identified 46 differential metabolites as potential biomarkers associated with 10 metabolic pathways, including arginine and proline metabolism. Network pharmacology suggested that LT exerts its hepatoprotective effects by regulating arginine metabolism and inflammatory factors; key components, such as caffeine and epigallocatechin gallate, showed direct relevance to NAFLD. Following the intervention, targeted metabolomic analysis revealed a significant change in the levels of 18 relevant amino acids, confirming LT's impact on arginine metabolism. Immunohistochemical results demonstrated reduced expression of inflammatory factors (TNF-α, IL-6, IL-1β) in the liver, suggesting improved liver health. Collectively, these findings indicate that LT mitigates HFD-induced NAFLD through regulation of amino acid metabolism and reduction of inflammatory factors, thereby alleviating liver injury.

六保茶通过精氨酸代谢改善高脂肪饮食诱导的非酒精性脂肪肝:来自代谢组学和网络药理学的见解
非酒精性脂肪性肝病(NAFLD)已成为一个突出的公共卫生问题,与代谢综合征密切相关。六保茶(LT)是一种传统的中国黑茶,通过调节新陈代谢而具有保护肝脏的作用。本研究采用代谢组学和网络药理学方法研究了肝移植对hfd诱导的NAFLD的保护作用。我们发现,肝移植显著降低了饲喂hfd大鼠的能量摄入,减轻了内脏脂肪的异常堆积,并预防了高脂血症、肝脏脂质异常沉积和肝脏脂肪变性。血清非靶向代谢组学分析确定了46种差异代谢物作为与10种代谢途径相关的潜在生物标志物,包括精氨酸和脯氨酸代谢。网络药理学提示,LT通过调节精氨酸代谢和炎症因子发挥保肝作用;关键成分,如咖啡因和表没食子儿茶素没食子酸酯,显示与NAFLD直接相关。干预后,靶向代谢组学分析显示18种相关氨基酸水平发生显著变化,证实了LT对精氨酸代谢的影响。免疫组化结果显示肝脏炎症因子(TNF-α、IL-6、IL-1β)表达降低,提示肝脏健康状况改善。综上所述,这些发现表明,LT通过调节氨基酸代谢和减少炎症因子来减轻hfd诱导的NAFLD,从而减轻肝损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biomedical Chromatography
Biomedical Chromatography 生物-分析化学
CiteScore
3.60
自引率
5.60%
发文量
268
审稿时长
2.3 months
期刊介绍: Biomedical Chromatography is devoted to the publication of original papers on the applications of chromatography and allied techniques in the biological and medical sciences. Research papers and review articles cover the methods and techniques relevant to the separation, identification and determination of substances in biochemistry, biotechnology, molecular biology, cell biology, clinical chemistry, pharmacology and related disciplines. These include the analysis of body fluids, cells and tissues, purification of biologically important compounds, pharmaco-kinetics and sequencing methods using HPLC, GC, HPLC-MS, TLC, paper chromatography, affinity chromatography, gel filtration, electrophoresis and related techniques.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信