• 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

倍半萜内酯:对抗炎症的有前景的天然化合物。

Sesquiterpene Lactones: Promising Natural Compounds to Fight Inflammation.

作者信息

Matos Melanie S, Anastácio José D, Nunes Dos Santos Cláudia

机构信息

Instituto de Biologia Experimental e Tecnológica (iBET), Apartado 12, 2781-901 Oeiras, Portugal.

Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.

出版信息

Pharmaceutics. 2021 Jun 30;13(7):991. doi: 10.3390/pharmaceutics13070991.

DOI:10.3390/pharmaceutics13070991
PMID:34208907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8309091/
Abstract

Inflammation is a crucial and complex process that reestablishes the physiological state after a noxious stimulus. In pathological conditions the inflammatory state may persist, leading to chronic inflammation and causing tissue damage. Sesquiterpene lactones (SLs) are composed of a large and diverse group of highly bioactive plant secondary metabolites, characterized by a 15-carbon backbone structure. In recent years, the interest in SLs has risen due to their vast array of biological activities beneficial for human health. The anti-inflammatory potential of these compounds results from their ability to target and inhibit various key pro-inflammatory molecules enrolled in diverse inflammatory pathways, and prevent or reduce the inflammatory damage on tissues. Research on the anti-inflammatory mechanisms of SLs has thrived over the last years, and numerous compounds from diverse plants have been studied, using in silico, in vitro, and in vivo assays. Besides their anti-inflammatory potential, their cytotoxicity, structure-activity relationships, and pharmacokinetics have been investigated. This review aims to gather the most relevant results and insights concerning the anti-inflammatory potential of SL-rich extracts and pure SLs, focusing on their effects in different inflammatory pathways and on different molecular players.

摘要

炎症是一个关键且复杂的过程,它能在有害刺激后重新建立生理状态。在病理状态下,炎症状态可能持续存在,导致慢性炎症并造成组织损伤。倍半萜内酯(SLs)是由一大类高度生物活性的植物次生代谢产物组成,其特征是具有15碳骨架结构。近年来,由于SLs对人类健康具有广泛的有益生物活性,人们对其兴趣日益增加。这些化合物的抗炎潜力源于它们能够靶向和抑制参与多种炎症途径的各种关键促炎分子,并预防或减少对组织的炎症损伤。过去几年,关于SLs抗炎机制的研究蓬勃发展,使用计算机模拟、体外和体内试验对来自不同植物的众多化合物进行了研究。除了它们的抗炎潜力外,还对它们的细胞毒性、构效关系和药代动力学进行了研究。本综述旨在收集有关富含SL的提取物和纯SLs抗炎潜力的最相关结果和见解,重点关注它们在不同炎症途径和不同分子参与者中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/78547b463266/pharmaceutics-13-00991-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/44174c15658f/pharmaceutics-13-00991-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/93f7a0cc0690/pharmaceutics-13-00991-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/8628771fb0e8/pharmaceutics-13-00991-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/3cf76cdb9c1a/pharmaceutics-13-00991-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/5ba9c4200863/pharmaceutics-13-00991-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/30f9235c668f/pharmaceutics-13-00991-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/3462b4ef6251/pharmaceutics-13-00991-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/44f589af6289/pharmaceutics-13-00991-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/a5b9a5ceab7c/pharmaceutics-13-00991-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/9f7bf5c5ff18/pharmaceutics-13-00991-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/78547b463266/pharmaceutics-13-00991-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/44174c15658f/pharmaceutics-13-00991-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/93f7a0cc0690/pharmaceutics-13-00991-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/8628771fb0e8/pharmaceutics-13-00991-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/3cf76cdb9c1a/pharmaceutics-13-00991-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/5ba9c4200863/pharmaceutics-13-00991-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/30f9235c668f/pharmaceutics-13-00991-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/3462b4ef6251/pharmaceutics-13-00991-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/44f589af6289/pharmaceutics-13-00991-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/a5b9a5ceab7c/pharmaceutics-13-00991-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/9f7bf5c5ff18/pharmaceutics-13-00991-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5f6/8309091/78547b463266/pharmaceutics-13-00991-g011.jpg

相似文献

1
Sesquiterpene Lactones: Promising Natural Compounds to Fight Inflammation.倍半萜内酯:对抗炎症的有前景的天然化合物。
Pharmaceutics. 2021 Jun 30;13(7):991. doi: 10.3390/pharmaceutics13070991.
2
Biological Activities of Sesquiterpene Lactones Isolated from the Genus Centaurea L. (Asteraceae).从菊科植物矢车菊属中分离得到的倍半萜内酯的生物活性。
Curr Pharm Des. 2017;23(19):2767-2786. doi: 10.2174/1381612823666170215113927.
3
Quantitative structure-activity relationship of sesquiterpene lactones as inhibitors of the transcription factor NF-kappaB.倍半萜内酯作为转录因子NF-κB抑制剂的定量构效关系
J Med Chem. 2004 Nov 18;47(24):6042-54. doi: 10.1021/jm049937r.
4
Anti-cancer potential of sesquiterpene lactones: bioactivity and molecular mechanisms.倍半萜内酯的抗癌潜力:生物活性与分子机制
Curr Med Chem Anticancer Agents. 2005 May;5(3):239-49. doi: 10.2174/1568011053765976.
5
Sesquiterpene lactones as drugs with multiple targets in cancer treatment: focus on parthenolide.倍半萜内酯类化合物作为癌症治疗多靶点药物的研究进展:以小白菊内酯为例。
Anticancer Drugs. 2012 Oct;23(9):883-96. doi: 10.1097/CAD.0b013e328356cad9.
6
Sesquiterpene Lactones from Artemisia Genus: Biological Activities and Methods of Analysis.蒿属植物中的倍半萜内酯:生物活性及分析方法
J Anal Methods Chem. 2015;2015:247685. doi: 10.1155/2015/247685. Epub 2015 Oct 1.
7
The genus Inula and their metabolites: from ethnopharmacological to medicinal uses.旋覆花属植物及其代谢产物:从民族药理学用途到药用价值。
J Ethnopharmacol. 2014 Jun 11;154(2):286-310. doi: 10.1016/j.jep.2014.04.010. Epub 2014 Apr 19.
8
Perspectives on sesquiterpene lactones in inflammation and cancer.倍半萜内酯类化合物在炎症和癌症中的作用。
Curr Drug Targets. 2011 Oct;12(11):1560-73. doi: 10.2174/138945011798109437.
9
Inhibition of transcription factor NF-kappaB by sesquiterpene lactones: a proposed molecular mechanism of action.倍半萜内酯对转录因子NF-κB的抑制作用:一种可能的分子作用机制。
Bioorg Med Chem. 1999 Nov;7(11):2343-52. doi: 10.1016/s0968-0896(99)00195-9.
10
Helenalin - A Sesquiterpene Lactone with Multidirectional Activity.**标题**:**Helenalin-一种具有多向活性的倍半萜内酯** **摘要**:Helenalin 是一种从菊科植物中分离得到的倍半萜内酯,其在各种细胞模型中表现出广泛的生物活性。本综述总结了 Helenalin 的生物学作用,包括抗增殖、抗炎、抗氧化、抗微生物和抗血管生成活性。此外,还讨论了 Helenalin 在体内模型中的作用,包括抗肿瘤、抗炎和抗纤维化作用。尽管 Helenalin 已在临床前研究中进行了广泛研究,但尚未在临床试验中进行评估。本综述强调了 Helenalin 在医学研究中的潜力,并强调了需要进行更多的临床前和临床试验来评估其作为治疗剂的潜力。
Curr Drug Targets. 2019;20(4):444-452. doi: 10.2174/1389450119666181012125230.

引用本文的文献

1
Biological and Medicinal Properties of Makino and Its Bioactive Products.牧野及其生物活性产物的生物学和药用特性。
Int J Mol Sci. 2025 Jun 20;26(13):5956. doi: 10.3390/ijms26135956.
2
Advancements in the therapeutic potential of sesquiterpenoids for the treatment of hepatocellular carcinoma (Review).倍半萜类化合物治疗肝细胞癌的治疗潜力进展(综述)
Int J Oncol. 2025 Jul;67(1). doi: 10.3892/ijo.2025.5766. Epub 2025 Jun 20.
3
The novel role of Aiton extracts as antidiabetic and anti-inflammatory functions in pancreatic Β cells exposed to hyperglycaemia.

本文引用的文献

1
Guaianolide Sesquiterpene Lactones from .从 中分离得到的愈创木烷型倍半萜内酯。
Molecules. 2021 Apr 3;26(7):2055. doi: 10.3390/molecules26072055.
2
Low Oral Bioavailability and Partial Gut Microbiotic and Phase II Metabolism of Brussels/Witloof Chicory Sesquiterpene Lactones in Healthy Humans.布鲁塞尔菊苣/菊苣苣苣烯类倍半萜在健康人体中的低口服生物利用度和部分肠道微生物和 II 相代谢。
Nutrients. 2020 Nov 28;12(12):3675. doi: 10.3390/nu12123675.
3
Assessing the Intestinal Permeability and Anti-Inflammatory Potential of Sesquiterpene Lactones from Chicory.
艾顿提取物在暴露于高血糖环境的胰腺β细胞中作为具有抗糖尿病和抗炎功能的新作用。
J Diabetes Metab Disord. 2025 Jun 2;24(1):136. doi: 10.1007/s40200-025-01654-0. eCollection 2025 Jun.
4
Xanthatin nanocrystals exert anti-inflammatory properties against TNFα-primed 2D monolayers and in 3D spheroids of human HT29 colorectal cancer cells.山苍子油精纳米晶体对经肿瘤坏死因子α预处理的人HT29结肠癌细胞二维单层和三维球体具有抗炎特性。
Discov Nano. 2025 May 19;20(1):83. doi: 10.1186/s11671-025-04257-z.
5
Natural sesquiterpene lactones in prostate cancer therapy: mechanisms and sources.前列腺癌治疗中的天然倍半萜内酯:作用机制与来源
Med Oncol. 2025 May 15;42(6):212. doi: 10.1007/s12032-025-02740-2.
6
Protective Effect of Artemisinin Against Luperox Induced Oxidative Stress and Insulin Resistance via Pi3k/Akt Pathway in Zebrafish Larvae.青蒿素通过PI3K/Akt通路对鲁珀罗克斯诱导的斑马鱼幼体氧化应激和胰岛素抵抗的保护作用
Cell Biochem Biophys. 2025 Apr 12. doi: 10.1007/s12013-025-01747-w.
7
Erioflorin and Erioflorin Acetate Induce Cell Death in Advanced Prostate Cancer Through ROS Increase and NF-κB Inhibition.毛花洋地黄苷元和毛花洋地黄苷元醋酸酯通过增加活性氧和抑制核因子κB诱导晚期前列腺癌细胞死亡。
J Xenobiot. 2025 Mar 18;15(2):45. doi: 10.3390/jox15020045.
8
Sesquiterpene Lactones as Promising Phytochemicals to Cease Metastatic Propagation of Cancer.倍半萜内酯作为有望阻止癌症转移扩散的植物化学物质。
Biomolecules. 2025 Feb 12;15(2):268. doi: 10.3390/biom15020268.
9
Sesquiterpene Lactones as Promising Anti-Glioblastoma Drug Candidates Exerting Complex Effects on Glioblastoma Cell Viability and Proneural-Mesenchymal Transition.倍半萜内酯作为有前景的抗胶质母细胞瘤候选药物,对胶质母细胞瘤细胞活力和神经前体-间充质转化产生复杂影响。
Biomedicines. 2025 Jan 8;13(1):133. doi: 10.3390/biomedicines13010133.
10
Exploring sesquiterpene lactones: structural diversity and antiviral therapeutic insights.探索倍半萜内酯:结构多样性与抗病毒治疗见解。
RSC Adv. 2025 Jan 22;15(3):1970-1988. doi: 10.1039/d4ra08125k. eCollection 2025 Jan 16.
评估菊苣倍半萜内酯对肠道通透性和抗炎潜力的影响。
Nutrients. 2020 Nov 19;12(11):3547. doi: 10.3390/nu12113547.
4
Human Gut Microbiota Metabolism of Dietary Sesquiterpene Lactones: Untargeted Metabolomics Study of Lactucopicrin and Lactucin Conversion In Vitro and In Vivo.膳食倍半萜烯内酯的人类肠道微生物群代谢:菊苣酸和菊苣内酯在体外和体内转化的非靶向代谢组学研究。
Mol Nutr Food Res. 2020 Nov;64(21):e2000619. doi: 10.1002/mnfr.202000619. Epub 2020 Oct 7.
5
Derivatisation of parthenolide to address chemoresistant chronic lymphocytic leukaemia.用于治疗化疗耐药性慢性淋巴细胞白血病的小白菊内酯衍生物
Medchemcomm. 2019 Aug 1;10(8):1379-1390. doi: 10.1039/c9md00297a.
6
Sesquiterpene fractions of plants as potent inhibitors of inducible nitric oxide synthase and cyclooxygenase-2 expression.植物中的倍半萜馏分作为诱导型一氧化氮合酶和环氧化酶-2表达的有效抑制剂。
Iran J Basic Med Sci. 2019 Jul;22(7):774-780. doi: 10.22038/ijbms.2019.34792.8249.
7
The Possible Anti-Inflammatory Effect of Dehydrocostus Lactone on DSS-Induced Colitis in Mice.脱氢木香内酯对葡聚糖硫酸钠诱导的小鼠结肠炎的可能抗炎作用
Evid Based Complement Alternat Med. 2020 Jan 30;2020:5659738. doi: 10.1155/2020/5659738. eCollection 2020.
8
Deoxyelephantopin decreases the release of inflammatory cytokines in macrophage associated with attenuation of aerobic glycolysis via modulation of PKM2.脱氧土大黄素通过调节 PKM2 减少与有氧糖酵解衰减相关的巨噬细胞中炎症细胞因子的释放。
Int Immunopharmacol. 2020 Feb;79:106048. doi: 10.1016/j.intimp.2019.106048. Epub 2019 Dec 18.
9
Suppressive effects of dehydrocostus lactone on the toll-like receptor signaling pathways.去氢木香内酯对 toll 样受体信号通路的抑制作用。
Int Immunopharmacol. 2020 Jan;78:106075. doi: 10.1016/j.intimp.2019.106075. Epub 2019 Dec 5.
10
Advances in chemistry and bioactivity of parthenolide.紫萍内酯的化学和生物活性研究进展。
Nat Prod Rep. 2020 Apr 1;37(4):541-565. doi: 10.1039/c9np00049f. Epub 2019 Nov 25.