• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于肠道微生物信息学和肝脏代谢组学深入探究紫锥菊多糖减轻小鼠酒精性肝损伤的机制

In-depth investigation of the mechanisms of Echinacea purpurea polysaccharide mitigating alcoholic liver injury in mice via gut microbiota informatics and liver metabolomics.

作者信息

Jiang Wenhao, Zhu Hongkang, Liu Chang, Hu Bin, Guo Yahui, Cheng Yuliang, Qian He

机构信息

State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China; Synergetic Innovation Center for Food Safety and Nutrition, Jiangnan University, Wuxi 214122, China.

School of Biotechnology, Jiangnan University, Wuxi 214122, China.

出版信息

Int J Biol Macromol. 2022 Jun 1;209(Pt A):1327-1338. doi: 10.1016/j.ijbiomac.2022.04.131. Epub 2022 Apr 21.

DOI:10.1016/j.ijbiomac.2022.04.131
PMID:35461865
Abstract

Accumulating evidence suggests that the pathogenesis of alcoholic liver disease (ALD) is strongly correlated with abnormalities of the gut-liver axis. Echinacea purpurea polysaccharide (EPP) is a homogeneous polysaccharide, which has been shown to mitigate ALD. However, the effects of EPP on gut microbiome and consequently on hepatic metabolism have yet to be explored. In this study, the microbiome and metabolomics were combined to explore the effects of EPP on gut microbiota and hepatic metabolism, and the relationship between both was further revealed by Spearman correlation analysis. Results exhibited EPP reversed alcohol-induced disturbances in gut microbiota, evidenced by increased abundance of Muribaculaceae, Lactobacillus, and Bacteroides and decreased abundance of Escherichia_Shigella and Enterococcus. Besides, EPP promoted the production of n-butyric acid, a short-chain fatty acid that maintains the integrity of the intestinal barrier. Moreover, EPP improved alterations in hepatic metabolites, and characteristic metabolites such as Berberine and Ponasterone as well as key metabolic pathways, particularly Nitrogen metabolism, were identified. Furthermore, correlation analysis suggested significant associations between gut microbes and hepatic metabolites, which in turn confirmed EPP alleviated ALD via the gut-liver axis. Therefore, these findings elucidated in-depth mechanisms of EPP against ALD and provided a new target for intervention in alcohol-related diseases.

摘要

越来越多的证据表明,酒精性肝病(ALD)的发病机制与肠-肝轴异常密切相关。紫锥菊多糖(EPP)是一种均质多糖,已被证明可减轻ALD。然而,EPP对肠道微生物群以及由此对肝脏代谢的影响尚未得到探索。在本研究中,将微生物组学和代谢组学相结合,以探索EPP对肠道微生物群和肝脏代谢的影响,并通过Spearman相关性分析进一步揭示两者之间的关系。结果显示,EPP逆转了酒精引起的肠道微生物群紊乱,表现为毛螺菌科、乳酸杆菌属和拟杆菌属丰度增加,而埃希氏菌属-志贺氏菌属和肠球菌属丰度降低。此外,EPP促进了短链脂肪酸正丁酸的产生,正丁酸可维持肠道屏障的完整性。此外,EPP改善了肝脏代谢物的变化,并鉴定出了小檗碱和蜕皮甾酮等特征性代谢物以及关键代谢途径,尤其是氮代谢。此外,相关性分析表明肠道微生物与肝脏代谢物之间存在显著关联,这反过来证实了EPP通过肠-肝轴减轻了ALD。因此,这些发现阐明了EPP对抗ALD的深入机制,并为酒精相关疾病的干预提供了新的靶点。

相似文献

1
In-depth investigation of the mechanisms of Echinacea purpurea polysaccharide mitigating alcoholic liver injury in mice via gut microbiota informatics and liver metabolomics.基于肠道微生物信息学和肝脏代谢组学深入探究紫锥菊多糖减轻小鼠酒精性肝损伤的机制
Int J Biol Macromol. 2022 Jun 1;209(Pt A):1327-1338. doi: 10.1016/j.ijbiomac.2022.04.131. Epub 2022 Apr 21.
2
The combination of microbiome and metabolome to analyze the cross-cooperation mechanism of polysaccharide with the gut microbiota and .从宏基因组和代谢组学角度分析多糖与肠道微生物群互作的协同机制。
Food Funct. 2022 Oct 3;13(19):10069-10082. doi: 10.1039/d2fo02336a.
3
Echinacea purpurea polysaccharide intervene in hepatocellular carcinoma via modulation of gut microbiota to inhibit TLR4/NF-κB pathway.紫锥菊多糖通过调节肠道微生物群抑制 TLR4/NF-κB 通路干预肝细胞癌。
Int J Biol Macromol. 2024 Mar;261(Pt 2):129917. doi: 10.1016/j.ijbiomac.2024.129917. Epub 2024 Feb 2.
4
Ameliorative effects of chlorogenic acid on alcoholic liver injury in mice via gut microbiota informatics.通过肠道微生物组信息学研究绿原酸对酒精性肝损伤小鼠的改善作用。
Eur J Pharmacol. 2022 Aug 5;928:175096. doi: 10.1016/j.ejphar.2022.175096. Epub 2022 Jun 10.
5
Echinacea purpurea polysaccharide prepared by fractional precipitation prevents alcoholic liver injury in mice by protecting the intestinal barrier and regulating liver-related pathways.紫锥菊多糖通过保护肠道屏障和调节肝脏相关途径预防小鼠酒精性肝损伤。
Int J Biol Macromol. 2021 Sep 30;187:143-156. doi: 10.1016/j.ijbiomac.2021.07.095. Epub 2021 Jul 20.
6
Bifidobacterium longum subsp. longum BL21 ameliorates alcoholic liver disease in mice through enhancement of the hepatic antioxidant capacity and modulation of the gut microbiota.长双歧杆菌亚种 longum BL21 通过增强肝脏抗氧化能力和调节肠道微生物群来改善小鼠的酒精性肝病。
J Appl Microbiol. 2023 Nov 1;134(11). doi: 10.1093/jambio/lxad251.
7
Cyanidin-3-O-Glucoside Alleviates Alcoholic Liver Injury via Modulating Gut Microbiota and Metabolites in Mice.矢车菊素 - 3 - O - 葡萄糖苷通过调节小鼠肠道微生物群和代谢产物减轻酒精性肝损伤。
Nutrients. 2024 Feb 29;16(5):694. doi: 10.3390/nu16050694.
8
MUP1 mediates urolithin A alleviation of chronic alcohol-related liver disease via gut-microbiota-liver axis.MUP1 通过肠道微生物群-肝脏轴介导尿石素 A 缓解慢性酒精性肝病。
Gut Microbes. 2024 Jan-Dec;16(1):2367342. doi: 10.1080/19490976.2024.2367342. Epub 2024 Jun 18.
9
Crosstalk between gut microbiota and host lipid metabolism in a mouse model of alcoholic liver injury by chronic baijiu or ethanol feeding.慢性白酒或乙醇喂养致酒精性肝损伤小鼠模型中肠道微生物群与宿主脂质代谢的相互作用。
Food Funct. 2022 Jan 24;13(2):596-608. doi: 10.1039/d1fo02892h.
10
Fucoidan from Apostichopus japonicus ameliorates alcoholic liver disease by regulating gut-liver axis homeostasis.来自刺参的岩藻聚糖通过调节肠-肝轴稳态改善酒精性肝病。
Int J Biol Macromol. 2024 Jun;270(Pt 1):132093. doi: 10.1016/j.ijbiomac.2024.132093. Epub 2024 May 4.

引用本文的文献

1
Lignans-rich extract of prevent alcohol-associated liver disease by regulating the gut microbiota and tryptophan metabolism.富含木脂素的提取物通过调节肠道微生物群和色氨酸代谢来预防酒精相关性肝病。
Curr Res Food Sci. 2025 Aug 19;11:101172. doi: 10.1016/j.crfs.2025.101172. eCollection 2025.
2
Therapeutic Potential of Kelp Fucoidan in Rebiosis of Gut Microflora and Immune Homeostasis in Cyclophosphamide-Induced Immunosuppressed Mice.海带岩藻聚糖对环磷酰胺诱导的免疫抑制小鼠肠道微生物群再生及免疫稳态的治疗潜力
Foods. 2025 Jul 29;14(15):2662. doi: 10.3390/foods14152662.
3
Exploring the Prevention of Lipid Deposition Caused by High-Fat Diet and Its Mechanism of Action of Fermented Juice Based on Liver Metabolomics and Gut Microbiota.
基于肝脏代谢组学和肠道微生物群探究发酵汁对高脂饮食引起的脂质沉积的预防作用及其作用机制
Food Sci Nutr. 2025 Jul 28;13(8):e70449. doi: 10.1002/fsn3.70449. eCollection 2025 Aug.
4
Food plants as adjuvant medicines: a review of protective effects and clinical potential in alcoholic liver disease.作为辅助药物的食用植物:对酒精性肝病保护作用及临床潜力的综述
Front Pharmacol. 2025 May 22;16:1586238. doi: 10.3389/fphar.2025.1586238. eCollection 2025.
5
A Butyrate-Yielding Dietary Supplement Prevents Acute Alcoholic Liver Injury by Modulating Nrf2-Mediated Hepatic Oxidative Stress and Gut Microbiota.丁酸产生膳食补充剂通过调节 Nrf2 介导的肝氧化应激和肠道微生物群预防急性酒精性肝损伤。
Int J Mol Sci. 2024 Aug 30;25(17):9420. doi: 10.3390/ijms25179420.
6
The role of gut microbiota, exosomes, and their interaction in the pathogenesis of ALD.肠道微生物群、外泌体及其相互作用在酒精性肝病发病机制中的作用。
J Adv Res. 2025 Jun;72:353-367. doi: 10.1016/j.jare.2024.07.002. Epub 2024 Jul 3.
7
The roles and potential mechanisms of plant polysaccharides in liver diseases: a review.植物多糖在肝脏疾病中的作用及潜在机制:综述
Front Pharmacol. 2024 Jun 20;15:1400958. doi: 10.3389/fphar.2024.1400958. eCollection 2024.
8
The gut-liver axis in fatty liver disease: role played by natural products.脂肪肝疾病中的肠-肝轴:天然产物所起的作用。
Front Pharmacol. 2024 Apr 15;15:1365294. doi: 10.3389/fphar.2024.1365294. eCollection 2024.
9
Hepatoprotective effects of peach gum polysaccharides against alcoholic liver injury: moderation of oxidative stress and promotion of lipid metabolism.桃胶多糖对酒精性肝损伤的保肝作用:减轻氧化应激和促进脂质代谢
Front Nutr. 2024 Jan 11;10:1325450. doi: 10.3389/fnut.2023.1325450. eCollection 2023.
10
Anti-Bordetella bronchiseptica effects of targeted bacteriophages via microbiome and metabolic mediated mechanisms.靶向噬菌体通过微生物组和代谢介导机制对支气管败血波氏杆菌的拮抗作用。
Sci Rep. 2023 Dec 8;13(1):21755. doi: 10.1038/s41598-023-49248-1.