Sesquiterpene lactones from Cichorium intybus exhibit potent anti-inflammatory and hepatoprotective effects by repression of NF-κB and enhancement of NRF2

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-03-13 Epub Date: 2025-02-02 DOI:10.1016/j.jep.2025.119439
Yan Zhou , Tian Wen , Shan Yang , Binru Meng , Jing Wei , Jing Zhang , Lun Wang , Xiaofei Shen
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Abstract

Ethnopharmacological relevance

Cichorium intybus is a traditional medicinal herb for hepatitis treatment in China and Europe. Sesquiterpene lactones are the main active ingredients in C. intybus. However, their structure-activity relationship (SAR) and molecular mechanisms of anti-inflammatory and hepatoprotective effects require further elucidation.

Aim of the study

To identify new sesquiterpene lactones from C. intybus, and further evaluate their anti-inflammatory effects, SAR, and mechanisms of anti-inflammatory and hepatoprotective properties.

Methods

Identification of sesquiterpene lactones from C. intybus using chromatographic fractionation, NMR, and mass spectrometry. The repression of inflammation was evaluated in RAW264.7 macrophages incubated with LPS. Western blotting was employed to investigate the anti-inflammatory mechanisms. The hepatoprotective effect was measured in LPS/D-galactosamine (D-GalN)-induced acute hepatitis in mice.

Results

We identified 3 new sesquiterpene lactones and 15 known analogues from C. intybus. SAR analysis showed that the α-methylene-γ-lactone moiety was essential for their anti-inflammatory properties. Furthermore, 8-deoxylactucin was identified as the most potent anti-inflammatory component in LPS-induced RAW264.7 macrophages by reduction of nitric oxide production via inhibiting iNOS expression, and suppression of IL-1β, IL-6, and TNF-α expression. Mechanistically, 8-deoxylactucin not only blocked LPS-induced IKKα/β phosphorylation, IκBα phosphorylation and degradation, and NF-κB nuclear accumulation, but also enhanced NRF2 expression and nuclear translocation, HO-1 and NQO1 expression, and reduced ROS generation in vitro. In vivo, 8-deoxylactucin mitigated LPS/D-GalN-induced acute hepatitis, which manifested as reduction in inflammatory infiltration, live injury, serum levels of AST and ALT, and production of pro-inflammatory cytokines and 4-hydroxynonenal.

Conclusion

8-Deoxylactucin, the sesquiterpene lactone isolated from C. intybus, exerted anti-inflammatory and hepatoprotective effects by blocking NF-κB activation and enhancing NRF2 activation.

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菊苣倍半萜内酯通过抑制NF-κB和增强NRF2而具有有效的抗炎和保肝作用。
民族药理学相关性:菊苣是中国和欧洲治疗肝炎的传统草药。倍半萜内酯是鸡胸草的主要有效成分。然而,它们的构效关系(SAR)以及抗炎和保肝作用的分子机制有待进一步阐明。目的:鉴定新的倍半萜内酯类化合物,进一步评价其抗炎作用、合成孔径(SAR)及其抗炎和保肝作用机制。方法:采用色谱分离、核磁共振、质谱等方法对滇菊中倍半萜内酯进行鉴定。在LPS孵育的RAW264.7巨噬细胞中评估炎症抑制作用。采用免疫印迹法研究其抗炎机制。在LPS/ d -半乳糖胺(D-GalN)诱导的急性肝炎中检测其肝保护作用。结果:鉴定出3个新的倍半萜内酯和15个已知的类似物。SAR分析表明,α-亚甲基-γ-内酯部分对其抗炎性能至关重要。此外,8-deoxylactucin被鉴定为lps诱导的RAW264.7巨噬细胞中最有效的抗炎成分,通过抑制iNOS表达和抑制IL-1β、IL-6和TNF-α表达来减少一氧化氮的产生。在机制上,8-脱氧肌动蛋白不仅阻断lps诱导的IKKα/β磷酸化、i -κB α磷酸化降解和NF-κB核积累,还能增强NRF2表达和核易位、HO-1和NQO1表达,减少体外ROS生成。在体内,8-脱氧肌动蛋白减轻了LPS/ d - galn诱导的急性肝炎,表现为炎症浸润、活损伤、血清AST和ALT水平降低,促炎细胞因子和4-羟基壬烯醛的产生减少。结论:8-Deoxylactucin是牛蒡子的倍半萜内酯,其作用机制是阻断NF-κB活化,增强NRF2活化,具有抗炎和保肝作用。
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D-GalN
来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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