Discovery of dibenzylbutane lignan LCA derivatives as potent anti-inflammatory agents†

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics MedChemComm Pub Date : 2024-04-23 DOI:10.1039/D4MD00053F
Zhen Wang, Juan Zhang, Conghao Gai, Jing Wang, Xiaobin Zhuo, Yan Song, Yan Zou, Peichao Zhang, Guige Hou, Qingguo Meng, Qingjie Zhao and Xiaoyun Chai
{"title":"Discovery of dibenzylbutane lignan LCA derivatives as potent anti-inflammatory agents†","authors":"Zhen Wang, Juan Zhang, Conghao Gai, Jing Wang, Xiaobin Zhuo, Yan Song, Yan Zou, Peichao Zhang, Guige Hou, Qingguo Meng, Qingjie Zhao and Xiaoyun Chai","doi":"10.1039/D4MD00053F","DOIUrl":null,"url":null,"abstract":"<p >Inflammation is the body's response to defence against infection or injury, and is associated with the progression of many diseases, such as inflammatory bowel disease (IBD) and rheumatoid arthritis (RA). LCA, a dibenzylbutane lignan extracted from the roots of traditional medicinal plant <em>Litsea cubeba</em> (Lour.) Pers., has demonstrated promising anti-inflammatory activity. In this study, a series of novel LCA derivatives were designed, synthesized, and evaluated for anti-inflammatory activity. Lipopolysaccharide (LPS)-induced RAW 264.7 cell model experiments showed that compound <strong>10h</strong> (at 20 μM of concentration) had the strongest inhibitory effect on NO release, and inhibited the secretion and gene expression levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α <em>in vitro.</em> In addition, western blot, immunofluorescence, and molecular docking showed that the anti-inflammatory mechanism of compound <strong>10h</strong> may be related to the nuclear factor (NF)-κB signalling pathway. <em>In vivo</em> studies based on a carrageenan-induced mouse paw edema model have shown significant anti-inflammatory activity of compound <strong>10h</strong> at 20 mg kg<small><sup>−1</sup></small>. Preliminary <em>in vitro</em> and <em>in vivo</em> studies indicate that compound <strong>10h</strong> has the potential to be developed as a novel anti-inflammatory agent.</p>","PeriodicalId":88,"journal":{"name":"MedChemComm","volume":" 6","pages":" 2114-2126"},"PeriodicalIF":3.5970,"publicationDate":"2024-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MedChemComm","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/md/d4md00053f","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

Abstract

Inflammation is the body's response to defence against infection or injury, and is associated with the progression of many diseases, such as inflammatory bowel disease (IBD) and rheumatoid arthritis (RA). LCA, a dibenzylbutane lignan extracted from the roots of traditional medicinal plant Litsea cubeba (Lour.) Pers., has demonstrated promising anti-inflammatory activity. In this study, a series of novel LCA derivatives were designed, synthesized, and evaluated for anti-inflammatory activity. Lipopolysaccharide (LPS)-induced RAW 264.7 cell model experiments showed that compound 10h (at 20 μM of concentration) had the strongest inhibitory effect on NO release, and inhibited the secretion and gene expression levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α in vitro. In addition, western blot, immunofluorescence, and molecular docking showed that the anti-inflammatory mechanism of compound 10h may be related to the nuclear factor (NF)-κB signalling pathway. In vivo studies based on a carrageenan-induced mouse paw edema model have shown significant anti-inflammatory activity of compound 10h at 20 mg kg−1. Preliminary in vitro and in vivo studies indicate that compound 10h has the potential to be developed as a novel anti-inflammatory agent.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
发现作为强效抗炎剂的二苄基丁烷木质素 LCA 衍生物
炎症是机体抵御感染或损伤的反应,与许多疾病的发展有关,如炎症性肠病(IBD)和类风湿性关节炎(RA)。LCA 是一种二苄基丁烷木质素,从传统药用植物 Litsea cubeba (Lour.) Pers.的根中提取,具有良好的抗炎活性。本研究设计、合成了一系列新型 LCA 衍生物,并对其抗炎活性进行了评估。脂多糖(LPS)诱导的 RAW 264.7 细胞模型实验表明,化合物 10h (浓度为 20 μM)对 NO 释放的抑制作用最强,并能抑制体外白细胞介素(IL)-1β、IL-6 和肿瘤坏死因子(TNF)-α 的分泌和基因表达水平。此外,Western 印迹、免疫荧光和分子对接表明,化合物 10h 的抗炎机制可能与核因子(NF)-κB 信号通路有关。基于卡拉胶诱导的小鼠爪水肿模型的体内研究表明,20 毫克/千克的化合物 10h 具有显著的抗炎活性。初步的体外和体内研究表明,化合物 10h 有潜力开发成一种新型抗炎药物。
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 去求助
来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
期刊最新文献
Back cover Introduction to the themed collection in honour of Professor Christian Leumann Back cover Correction: computational design, synthesis, and assessment of 3-(4-(4-(1,3,4-oxadiazol-2-yl)-1H-imidazol-2-yl)phenyl)-1,2,4-oxadiazole derivatives as effective epidermal growth factor receptor inhibitors: a prospective strategy for anticancer therapy Introduction to the themed collection on ‘AI in Medicinal Chemistry’
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1