发现作为强效抗炎剂的二苄基丁烷木质素 LCA 衍生物

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
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引用次数: 0

摘要

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。

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

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.

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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.
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