• 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

在预防酒精性肝病进展中的作用:全成分佛手精油及其主要成分D-柠檬烯的比较研究

Role in Preventing Alcoholic Liver Disease Progression: A Comparative Study of Whole-Component Finger Citron Essential Oil and Its Major Component D-Limonene.

作者信息

Chen Jingxin, Ou Genghua, Gu Wenting, Shi Jian, Lyu Ruiying, Wu Xueping, Wang Junming, Liu Chunhong

机构信息

College of Food Science, South China Agricultural University, Guangzhou 510642, China.

Guangdong Provincial Key Laboratory of Food Quality and Safety, Guangzhou 510642, China.

出版信息

Nutrients. 2025 Apr 3;17(7):1255. doi: 10.3390/nu17071255.

DOI:10.3390/nu17071255
PMID:40219012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11990129/
Abstract

: Chronic alcohol overconsumption triggers alcohol liver injury, and therapeutic strategies targeting alcohol-triggered oxidative stress and hepatic inflammatory responses represent potential approaches to ameliorating alcohol-related hepatotoxicity. This study aimed to determine the hepatoprotective activity of finger citron essential oil (FCEO) in alcoholic liver disease (ALD)-afflicted rats and explore its underlying mechanisms. In order to identify the effective components, we compared the effects of FCEO and D-limonene. : The regulatory effects of FCEO on metabolic enzymes were systematically evaluated through in vitro experiments. In vivo studies were conducted to investigate and compare the hepatoprotective effects of FCEO and D-limonene. Staining methods, assay kits, and Western Blot were used to determine the roles of FCEO and D-limonene in the ALD rats. : We found that FCEO downregulated phase I metabolic enzymes and upregulated phase II metabolic enzymes in Buffalo Rat Liver-3A (BRL-3A) cells. FCEO and/or D-limonene intervention reduced transaminase levels in ALD rats and effectively alleviated inflammatory cell infiltration and lipid droplet accumulation in their liver tissue. Additionally, FCEO and D-limonene played a regulatory role in oxidative stress and inflammation-related pathways such as the MAPK/Nrf2 and NF-κB/AMPK pathways. FCEO was superior to D-limonene as an antioxidant in alleviating alcoholic liver injury. : This study revealed the alleviative effects and mechanisms of FCEO on alcoholic liver injury, demonstrating better efficacy compared to its monomer, thus providing a strategy for the development and utilization of finger citron resources.

摘要

长期过量饮酒会引发酒精性肝损伤,针对酒精引发的氧化应激和肝脏炎症反应的治疗策略是改善酒精相关肝毒性的潜在方法。本研究旨在确定佛手柑精油(FCEO)对酒精性肝病(ALD)大鼠的肝保护活性,并探讨其潜在机制。为了确定有效成分,我们比较了FCEO和D-柠檬烯的效果。通过体外实验系统评估了FCEO对代谢酶的调节作用。进行体内研究以调查和比较FCEO和D-柠檬烯的肝保护作用。使用染色方法、检测试剂盒和蛋白质免疫印迹法来确定FCEO和D-柠檬烯在ALD大鼠中的作用。我们发现FCEO下调了水牛大鼠肝-3A(BRL-3A)细胞中的I相代谢酶,并上调了II相代谢酶。FCEO和/或D-柠檬烯干预降低了ALD大鼠的转氨酶水平,并有效减轻了其肝组织中的炎性细胞浸润和脂滴积累。此外,FCEO和D-柠檬烯在氧化应激和炎症相关途径(如MAPK/Nrf2和NF-κB/AMPK途径)中发挥调节作用。作为抗氧化剂,FCEO在减轻酒精性肝损伤方面优于D-柠檬烯。本研究揭示了FCEO对酒精性肝损伤的缓解作用及其机制,表明其疗效优于其单体,从而为佛手柑资源的开发利用提供了策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/46a120400011/nutrients-17-01255-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/344ff19af007/nutrients-17-01255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/ce8d513226f0/nutrients-17-01255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/ed60c02579fb/nutrients-17-01255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/d16073fbaaf2/nutrients-17-01255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/4c38e6b3b398/nutrients-17-01255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/e6ec92c4a1be/nutrients-17-01255-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/46a120400011/nutrients-17-01255-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/344ff19af007/nutrients-17-01255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/ce8d513226f0/nutrients-17-01255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/ed60c02579fb/nutrients-17-01255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/d16073fbaaf2/nutrients-17-01255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/4c38e6b3b398/nutrients-17-01255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/e6ec92c4a1be/nutrients-17-01255-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5650/11990129/46a120400011/nutrients-17-01255-g007.jpg

相似文献

1
Role in Preventing Alcoholic Liver Disease Progression: A Comparative Study of Whole-Component Finger Citron Essential Oil and Its Major Component D-Limonene.在预防酒精性肝病进展中的作用:全成分佛手精油及其主要成分D-柠檬烯的比较研究
Nutrients. 2025 Apr 3;17(7):1255. doi: 10.3390/nu17071255.
2
Anti-inflammatory effect of essential oil and its constituents from fingered citron (Citrus medica L. var. sarcodactylis) through blocking JNK, ERK and NF-κB signaling pathways in LPS-activated RAW 264.7 cells.佛手精油及其成分通过阻断 LPS 激活的 RAW 264.7 细胞中的 JNK、ERK 和 NF-κB 信号通路发挥抗炎作用。
Food Chem Toxicol. 2013 Jul;57:126-31. doi: 10.1016/j.fct.2013.03.017. Epub 2013 Mar 26.
3
Sedative-Hypnotic Effect and Mechanism of Carbon Nanofiber Loaded with Essential Oils of ( Hort.) and Finger Citron ( L. var. ) on Mice Models of Insomnia.载药碳纤维对失眠症模型小鼠的镇静催眠作用及机制研究。
Biomolecules. 2024 Sep 2;14(9):1102. doi: 10.3390/biom14091102.
4
Baicalin Attenuates Alcoholic Liver Injury through Modulation of Hepatic Oxidative Stress, Inflammation and Sonic Hedgehog Pathway in Rats.黄芩苷通过调节大鼠肝脏氧化应激、炎症和音猬因子信号通路减轻酒精性肝损伤。
Cell Physiol Biochem. 2016;39(3):1129-40. doi: 10.1159/000447820. Epub 2016 Aug 29.
5
Qiwei Jinggan Ling regulates oxidative stress and lipid metabolism in alcoholic liver disease by activating AMPK.芪味清肝灵通过激活 AMPK 调节酒精性肝病的氧化应激和脂质代谢。
Phytomedicine. 2024 Dec;135:156125. doi: 10.1016/j.phymed.2024.156125. Epub 2024 Oct 4.
6
The diabetes medication Canagliflozin attenuates alcoholic liver disease by reducing hepatic lipid accumulation via SIRT1-AMPK-mTORC1 signaling pathway.糖尿病药物卡格列净通过SIRT1-AMPK-mTORC1信号通路减少肝脏脂质积累,从而减轻酒精性肝病。
Eur J Pharmacol. 2025 Apr 5;992:177320. doi: 10.1016/j.ejphar.2025.177320. Epub 2025 Feb 8.
7
Ferulic acid from Angelica sinensis (Oliv.) Diels ameliorates lipid metabolism in alcoholic liver disease via AMPK/ACC and PI3K/AKT pathways.当归中的阿魏酸通过AMPK/ACC和PI3K/AKT途径改善酒精性肝病中的脂质代谢。
J Ethnopharmacol. 2025 Feb 10;338(Pt 3):119118. doi: 10.1016/j.jep.2024.119118. Epub 2024 Nov 17.
8
Chronic intermittent hypoxia alleviates alcohol-related liver injury via downregulation of hepatic hypoxia-inducible factor-2α.慢性间歇性低氧通过下调肝脏缺氧诱导因子-2α减轻酒精相关性肝损伤。
Am J Physiol Gastrointest Liver Physiol. 2025 May 1;328(5):G610-G623. doi: 10.1152/ajpgi.00283.2024. Epub 2025 Apr 17.
9
Antibacterial Activity and Mechanisms of Essential Oil from .香芹酚精油的抑菌活性及作用机制。
Molecules. 2019 Apr 22;24(8):1577. doi: 10.3390/molecules24081577.
10
An integrated network pharmacology approach reveals that Ampelopsis grossedentata improves alcoholic liver disease via TLR4/NF-κB/MLKL pathway.基于整合网络药理学的方法揭示,白首乌通过 TLR4/NF-κB/MLKL 通路改善酒精性肝病。
Phytomedicine. 2024 Sep;132:155658. doi: 10.1016/j.phymed.2024.155658. Epub 2024 May 4.

引用本文的文献

1
Chemical Profiling and Assessment of Analgesic and Anti-Inflammatory Activity of Essential Oil: In Vitro, In Vivo, and In Silico Studies.精油的化学剖析及其镇痛和抗炎活性评估:体外、体内和计算机模拟研究
Pharmaceuticals (Basel). 2025 Apr 27;18(5):635. doi: 10.3390/ph18050635.

本文引用的文献

1
Thirty years of NRF2: advances and therapeutic challenges.NRF2的三十年:进展与治疗挑战
Nat Rev Drug Discov. 2025 Mar 4. doi: 10.1038/s41573-025-01145-0.
2
New insights in the pathogenesis of alcohol-related liver disease: The metabolic, immunologic, and neurologic pathways.酒精性肝病发病机制的新见解:代谢、免疫和神经途径。
Liver Res. 2022 Oct 3;7(1):1-8. doi: 10.1016/j.livres.2022.09.004. eCollection 2023 Mar.
3
Involvement of p38 MAPK and MAPKAPK2 in promoting cell death and the inflammatory response to ischemic stress associated with necrotic glioblastoma.
p38丝裂原活化蛋白激酶(p38 MAPK)和丝裂原活化蛋白激酶激活的蛋白激酶2(MAPKAPK2)参与促进细胞死亡以及对与坏死性胶质母细胞瘤相关的缺血应激的炎症反应。
Cell Death Dis. 2025 Jan 14;16(1):12. doi: 10.1038/s41419-025-07335-3.
4
Mechanism of action of Nrf2 and its related natural regulators in rheumatoid arthritis.Nrf2 及其相关天然调节剂在类风湿关节炎中的作用机制。
J Orthop Surg Res. 2024 Nov 14;19(1):759. doi: 10.1186/s13018-024-05221-w.
5
Schisandra chinensis polysaccharide prevents alcohol-associated liver disease in mice by modulating the gut microbiota-tryptophan metabolism-AHR pathway axis.五味子多糖通过调节肠道微生物群-色氨酸代谢-AHR途径轴预防小鼠酒精性肝病。
Int J Biol Macromol. 2024 Dec;282(Pt 2):136843. doi: 10.1016/j.ijbiomac.2024.136843. Epub 2024 Oct 24.
6
Mitochondrial quality control in alcohol-associated liver disease.酒精相关性肝病中的线粒体质量控制。
Hepatol Commun. 2024 Oct 24;8(11). doi: 10.1097/HC9.0000000000000534. eCollection 2024 Nov 1.
7
Pursh extract ameliorates alcohol-related fatty liver disease in mice via the SIRT1/AMPK signaling axis.朴尔提取物通过SIRT1/AMPK信号轴改善小鼠酒精性脂肪肝疾病。
Heliyon. 2024 May 16;10(11):e31195. doi: 10.1016/j.heliyon.2024.e31195. eCollection 2024 Jun 15.
8
ELMO1 ameliorates intestinal epithelial cellular senescence via SIRT1/p65 signaling in inflammatory bowel disease-related fibrosis.ELMO1通过SIRT1/p65信号通路改善炎症性肠病相关纤维化中的肠上皮细胞衰老。
Gastroenterol Rep (Oxf). 2024 May 14;12:goae045. doi: 10.1093/gastro/goae045. eCollection 2024.
9
Role of inflammasomes and cytokines in immune dysfunction of liver cirrhosis.炎症小体和细胞因子在肝硬化免疫功能障碍中的作用。
Cytokine. 2023 Oct;170:156347. doi: 10.1016/j.cyto.2023.156347. Epub 2023 Aug 26.
10
Nutritional Support for Alcoholic Liver Disease.酒精性肝病的营养支持。
Nutrients. 2023 Mar 10;15(6):1360. doi: 10.3390/nu15061360.