Feibing Huang, Muhammad Aamer, Jara Muhdin Aliye, Yong Yang, Yu Mao, Qingling Xie, Hanwen Yuan, Yuqing Jian, Wei Wang
{"title":"penananum根中黄酮类化合物的抗炎活性。","authors":"Feibing Huang, Muhammad Aamer, Jara Muhdin Aliye, Yong Yang, Yu Mao, Qingling Xie, Hanwen Yuan, Yuqing Jian, Wei Wang","doi":"10.1016/j.jep.2025.120360","DOIUrl":null,"url":null,"abstract":"<p><strong>Ethnopharmacological relevance: </strong>Pronephrium penangianum, a traditional Chinese Tujia Ethnomedicine, is commonly used to treat various inflammatory conditions, including strains, dysentery, and traumatic injuries.</p><p><strong>Aim of the study: </strong>The study aimed to examine the anti-inflammatory activity of flavanones isolated from the roots of P. penangianum.</p><p><strong>Material and methods: </strong>Extensive spectrometric and spectroscopic techniques, including HRESI-MS, 1D and 2D-NMR spectra, and CD experiments, were used to elucidate the structures of the compounds. RAW264.7 cells were used for the anti-inflammatory assay. Griess reagent method, CCK-8 cell viability assay, Enzyme-linked immunosorbent assay (ELISA), molecular docking, and Western blot experiments to assess the related mechanism.</p><p><strong>Results: </strong>Five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12), were purified from the roots of P. penangianum. Activity screening of these compounds indicated that 6 significantly inhibited the release of NO, TNF-α, and IL-6. The in-silico study of 6, examining its interactions with IL-6 and p65.</p><p><strong>Conclusion: </strong>The phytochemical analysis of P. penangianum's roots resulted in five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12). The structures of the compounds were elucidated using spectroscopic and spectrometric analysis. Compound 6 exhibited potent anti-inflammatory effects associated with NF-κB activation by inhibiting IKBα phosphorylation and p65 degradation. To predict key interactions, compound 6 was also examined using molecular docking studies.</p>","PeriodicalId":15761,"journal":{"name":"Journal of ethnopharmacology","volume":" ","pages":"120360"},"PeriodicalIF":5.4000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-inflammatory activity of flavanones isolated from the roots of Pronephrium penangianum.\",\"authors\":\"Feibing Huang, Muhammad Aamer, Jara Muhdin Aliye, Yong Yang, Yu Mao, Qingling Xie, Hanwen Yuan, Yuqing Jian, Wei Wang\",\"doi\":\"10.1016/j.jep.2025.120360\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Ethnopharmacological relevance: </strong>Pronephrium penangianum, a traditional Chinese Tujia Ethnomedicine, is commonly used to treat various inflammatory conditions, including strains, dysentery, and traumatic injuries.</p><p><strong>Aim of the study: </strong>The study aimed to examine the anti-inflammatory activity of flavanones isolated from the roots of P. penangianum.</p><p><strong>Material and methods: </strong>Extensive spectrometric and spectroscopic techniques, including HRESI-MS, 1D and 2D-NMR spectra, and CD experiments, were used to elucidate the structures of the compounds. RAW264.7 cells were used for the anti-inflammatory assay. Griess reagent method, CCK-8 cell viability assay, Enzyme-linked immunosorbent assay (ELISA), molecular docking, and Western blot experiments to assess the related mechanism.</p><p><strong>Results: </strong>Five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12), were purified from the roots of P. penangianum. Activity screening of these compounds indicated that 6 significantly inhibited the release of NO, TNF-α, and IL-6. The in-silico study of 6, examining its interactions with IL-6 and p65.</p><p><strong>Conclusion: </strong>The phytochemical analysis of P. penangianum's roots resulted in five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12). The structures of the compounds were elucidated using spectroscopic and spectrometric analysis. Compound 6 exhibited potent anti-inflammatory effects associated with NF-κB activation by inhibiting IKBα phosphorylation and p65 degradation. To predict key interactions, compound 6 was also examined using molecular docking studies.</p>\",\"PeriodicalId\":15761,\"journal\":{\"name\":\"Journal of ethnopharmacology\",\"volume\":\" \",\"pages\":\"120360\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of ethnopharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jep.2025.120360\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of ethnopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jep.2025.120360","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Anti-inflammatory activity of flavanones isolated from the roots of Pronephrium penangianum.
Ethnopharmacological relevance: Pronephrium penangianum, a traditional Chinese Tujia Ethnomedicine, is commonly used to treat various inflammatory conditions, including strains, dysentery, and traumatic injuries.
Aim of the study: The study aimed to examine the anti-inflammatory activity of flavanones isolated from the roots of P. penangianum.
Material and methods: Extensive spectrometric and spectroscopic techniques, including HRESI-MS, 1D and 2D-NMR spectra, and CD experiments, were used to elucidate the structures of the compounds. RAW264.7 cells were used for the anti-inflammatory assay. Griess reagent method, CCK-8 cell viability assay, Enzyme-linked immunosorbent assay (ELISA), molecular docking, and Western blot experiments to assess the related mechanism.
Results: Five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12), were purified from the roots of P. penangianum. Activity screening of these compounds indicated that 6 significantly inhibited the release of NO, TNF-α, and IL-6. The in-silico study of 6, examining its interactions with IL-6 and p65.
Conclusion: The phytochemical analysis of P. penangianum's roots resulted in five new flavanone glycosides, jixueqisus G-K (1-5), and seven known flavonoid derivatives (6-12). The structures of the compounds were elucidated using spectroscopic and spectrometric analysis. Compound 6 exhibited potent anti-inflammatory effects associated with NF-κB activation by inhibiting IKBα phosphorylation and p65 degradation. To predict key interactions, compound 6 was also examined using molecular docking studies.
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.