Article(id=1322927796032504049, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.08.024, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793340165384, onlineDateStr=2026-10-30, pubDate=1754755200000, pubDateStr=2025-08-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793340165384, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793340165384, creator=13701087609, updateTime=1793340165384, updator=13701087609, issue=Issue{id=1322926217711726961, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='8', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1754755200000', pubDateStr='2025-08-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339789083, creator='13701087609', updateTime=1793340517761, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322929274071679978, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322929274071679979, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=116, endPage=118, ext={EN=ArticleExt(id=1322927796326105330, articleId=1322927796032504049, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Arctigenin Plays an Anti-inflammatory Role in Inhibiting Pyroptosis Mediated by NLRP3 Inflammasome, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the protective effect and intervention mechanism of arctigenin on lipopolysaccharide(LPS)combined with adenosine triphosphate(ATP)-stimulated pyroptosis in RAW264.7 cells.
Methods CCK8 assay was used to detect the effects of different concentrations of arctigenin on the viability of RAW264.7 cells;CCK8 assay was used to detect the effects of intervention of arctigenin(20,40,80μmol/L)on the viability of RAW264.7 cells induced by LPS+ATP;LDH release was used to detect the cellular membrane damage;ELISA was used to detect tumour necrosis factor-α(TNF-α),interleukin-6(IL-6)and IL-1βin cell supernatant;Western blotting was used to detect intracellular NLRP3,Caspase-1 p20,Caspase-1 p45,GSDMD-N and GSDMD-FL protein expression;the number of positive cells stained with propidium iodide(PI)was observed by forward and inverted fluorescence microscopy.
Results Arctigenin concentration less than 160μmol/L had little effect on cell viability;arctigenin(20,40,80μmol/L)intervention reversed the LPS+ATP-induced decrease in cell viability;arctigenin reduced LPS+ATP-induced release of LDH from pyroptosis cells as well as the number of PI-positive cells;arctigenin reduced LPS+ATP-induced LDH release from pyroptosis cells as well as the number of PI-positive cells;arctigenin inhibited the secretion of pro-inflammatory cytokines TNF-α,IL-6 and IL-1βby pyroptosis cells;arctigenin inhibited the expression of NLRP3,Caspase-1 p20,Caspase-1 p45,GSDMD-N and GSDMD-FL proteins in pyroptosis cells that inhibited the activation of NLRP3 inflammasome.
Conclusion Arctigenin inhibits NLRP3 inflammasome activation to improve pyroptosis and alleviate inflammatory responses.
, authors=Yuhui MA, Jialei MENG, Luyao QI, Yuan LIU, Xiaoxiao LI, Ming LEI, authorsList=Yuhui MA, Jialei MENG, Luyao QI, Yuan LIU, Xiaoxiao LI, Ming LEI, authorCompany=null, correspAuthors=Ming LEI, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322927801006948610, articleId=1322927796032504049, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=牛蒡子苷元抑制NLRP3炎症小体介导的细胞焦亡发挥抗炎作用, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 探讨牛蒡子苷元对脂多糖(LPS)联合三磷酸腺苷(ATP)刺激的RAW264.7细胞焦亡的保护作用及干预机制。
方法 CCK8法检测不同浓度的牛蒡子苷元对RAW264.7细胞活力的影响;CCK8法检测牛蒡子苷元(20、40、80 μmol/L)干预对LPS+ATP诱导的RAW264.7细胞活力的影响;乳酸脱氢酶(LDH)释放检测细胞膜损伤;ELISA法检测细胞上清液中肿瘤坏死因子-α(Tumor necrosis factor-α,TNF-α)、白细胞介素(Interleukin,IL)-6和IL-1β的含量;蛋白免疫印迹法(Western blotting)检测细胞内寡聚化结构域样受体蛋白3(NOD-like receptor thermal protein domain associated protein 3,NLRP3)、半胱天冬酶-1(Caspase-1)p20、Caspase-1 p45、GSDMD-N和GSDMD-FL蛋白的表达;正倒置荧光显微镜观察碘化丙啶(PI)染色阳性细胞数量。
结果 牛蒡子苷元浓度小于160μmol/L时对细胞活性影响较小;牛蒡子苷元(20、40、80μmol/L)干预逆转了LPS+ATP诱导的细胞活力降低;牛蒡子苷元减少了LPS+ATP诱导的焦亡细胞LDH的释放以及PI阳性细胞数量;牛蒡子苷元抑制焦亡细胞分泌促炎细胞因子TNF-α、IL-6和IL-1β;牛蒡子苷元抑制焦亡细胞NLRP3、Caspase-1 p20、Caspase-1 p45、GSDMD-N和GSDMD-FL蛋白的表达,抑制NLRP3炎症小体的激活。
结论 牛蒡子苷元抑制NLRP3炎症小体激活改善细胞焦亡,缓解炎症反应。
, authors=马宇慧, 孟佳磊, 齐璐瑶, 刘愿, 李笑笑, 雷鸣, authorsList=马宇慧, 孟佳磊, 齐璐瑶, 刘愿, 李笑笑, 雷鸣, authorCompany=null, correspAuthors=雷鸣, authorNote=
马宇慧(1996-),女,安徽阜阳人,博士在读,研究方向:中西医结合急危重症。
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马宇慧(1996-),女,安徽阜阳人,博士在读,研究方向:中西医结合急危重症。
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马宇慧(1996-),女,安徽阜阳人,博士在读,研究方向:中西医结合急危重症。
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不同浓度牛蒡子苷元对RAW264.7细胞活力的影响, figureFileSmall=NJLcciYNNYK3fSJ20goJ9w==, figureFileBig=0Nqxey3cQfMPh/ajsst3Ig==, tableContent=null), ArticleFig(id=1322927805364830510, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322927796032504049, language=EN, label=null, caption=null, figureFileSmall=OWJHRFLaV5iH7erOHhXepQ==, figureFileBig=VZsvASmfw3So6Zkp/xkdrw==, tableContent=null), ArticleFig(id=1322927805494853935, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322927796032504049, language=CN, label=图2, caption=
牛蒡子苷元对LPS联合ATP诱导的RAW264.7细胞活力的影响注:****与对照组相比,P<0.000 1;#与模型组相比,P<0.05;##与模型组相比,P<0.01;####与模型组相比,P<0.000 1。
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牛蒡子苷元对RAW264.7细胞焦亡模型LDH释放量的影响注:****与对照组相比,P<0.000 1;###与模型组相比,P<0.001;####与模型组相比,P<0.000 1。
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牛蒡子苷元对RAW264.7细胞焦亡模型TNF-α、IL-6、IL-1β释放量的影响注:****与对照组相比,P<0.000 1;####与模型组相比,P<0.000 1。
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牛蒡子苷元对RAW264.7细胞焦亡相关蛋白水平的影响注:****与对照组相比,P<0.000 1;#与模型组相比,P<0.05;##与模型组相比,P<0.01;####与模型组相比,P<0.000 1。
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牛蒡子苷元抑制LPS+ATP诱导的RAW264.7细胞焦亡(×20)注:****与对照组相比,P<0.000 1;###与模型组相比,P<0.001;####与模型组相比,P<0.000 1。
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