[Abstract]Objectives : Inthisstudy,weinvestigatedtheanti-inflammatoryandanti-oxidativeeffectsof MOK,apharmacopuncturemedicine,inlipopolysaccharide(LPS)-stimulatedmouseperitoneal macrophages. Methods : PeritonealmacrophageswereisolatedfromICRmice.Primarymacrophageswere treatedwithMOKextract(1.25,2.5,5,10,and20mg/ml)for30minandthenstimulatedwith LPS(1μg/ml)fortheindicatedtimes.CytotoxicitywasmeasuredusingMTTandLDHassays. Nitricoxide(NO)productioninculturesupernatantswasmeasuredusingtheGriessassay. ThemRNAexpressionofiNOS,COX-2,proinflammatorycytokines(TNF-α,IL-1β,andIL-6) andantioxidantenzymes(HO-1andMnSOD)wasmeasuredbyRT-PCR. Results : TreatmentwithMOKextract(2.5,5,and10mg/ml)significantlydecreasedLPS-induced NOproductioninperitonealmacrophagesthroughinhibitionofiNOSexpression.Theexpression of COX-2, TNF-α, IL-1β, and IL-6 mRNA was also decreased in LPS-stimulated macrophagesupontreatmentwithMOKextract.MOKtreatmentalsoincreasedtheexpression ofHO-1andMnSODmRNAinmacrophages. Conclusion : TheseresultsindicatethatMOKexertsanti-inflammatoryandantioxidanteffects byregulatingthetranscriptionlevelsofinflammatorymediatorsandantioxidantproteinsin activatedmacrophages.※ ThisresearchwassupportedbytheKoreanHealthTechnologyR&DProjectthroughtheKorean HealthIndustryDevelopmentInstitute(KHIDI)fundedbytheMinistryofHealth&Welfare,Republic ofKorea(grantnumber:HI16C0622).