Chlorophyllin suppression of lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells

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dc.contributor.authorCho, KJko
dc.contributor.authorHan, SHko
dc.contributor.authorKim, BYko
dc.contributor.authorHwang, SGko
dc.contributor.authorPark, KKko
dc.contributor.authorYang, KHko
dc.contributor.authorChung, An Sikko
dc.date.accessioned2013-02-27T13:27:37Z-
dc.date.available2013-02-27T13:27:37Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2000-07-
dc.identifier.citationTOXICOLOGY AND APPLIED PHARMACOLOGY, v.166, no.2, pp.120 - 127-
dc.identifier.issn0041-008X-
dc.identifier.urihttp://hdl.handle.net/10203/68841-
dc.description.abstractChlorophyllin (CHL), a water-soluble derivative of chlorophyll, functions as an anticarcinogen and antioxidant. In the present study, we investigated the effect of CHL on nitric oxide production in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Treatment with CHL inhibited nitric oxide production in the LPS-stimulated RAW 264.7 cells in a dose-related manner. Competitive RT-PCR analysis, using a DNA competitor as an internal standard, demonstrated that the treatment with 1, 10, and 50 mu M CHL decreased LPS-induced iNOS mRNA expression in a concentration-dependent manner. Since the expression of the iNOS gene is mainly regulated by NF-kappa B, we then examined the effects of CHL on the NF-kappa B DNA binding activity, using an electrophoretic mobility shift assay. CHL down-regulated the NF-kappa B DNA binding on its cognate recognition site at the concentrations just noted. Employing a transfection and reporter gene expression system with p(NF-kappa B)(3)-chloramphenicol acetyl transferase (CAT), the treatment of CHL produced a dose-dependent inhibition of CAT activity in RAW 264.7 cells. Furthermore, CHL partially restored LPS-decreased I kappa B alpha, an inhibitory protein against NF-kappa B activation, in the cytosolic extract from the LPS-treated cells determined by immunoblot analysis. CHL also protected the hydroxyl radical-induced cytotoxicity in RAW 264.7 cells, indicating its antioxidant effect. These results suggest that CHL suppresses the nitric oxide production and iNOS mRNA expression mediated by the inhibition of NF-kappa B activation, and its action mechanism may be based on its antioxidant effect. (C) 2000 Academic Press.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC Elsevier Science-
dc.subjectNF-KAPPA-B-
dc.subjectPERITONEAL-MACROPHAGES-
dc.subjectINHIBITS INDUCTION-
dc.subjectSYNTHASE GENE-
dc.subjectIN-VIVO-
dc.subjectTRANSCRIPTION FACTOR-
dc.subjectPEROXYNITRITE CAUSES-
dc.subjectOXIDATIVE STRESS-
dc.subjectINTERFERON-GAMMA-
dc.subjectDNA-BINDING-
dc.titleChlorophyllin suppression of lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells-
dc.typeArticle-
dc.identifier.wosid000088525700006-
dc.type.rimsART-
dc.citation.volume166-
dc.citation.issue2-
dc.citation.beginningpage120-
dc.citation.endingpage127-
dc.citation.publicationnameTOXICOLOGY AND APPLIED PHARMACOLOGY-
dc.identifier.doi10.1006/taap.2000.8958-
dc.contributor.nonIdAuthorCho, KJ-
dc.contributor.nonIdAuthorHan, SH-
dc.contributor.nonIdAuthorKim, BY-
dc.contributor.nonIdAuthorHwang, SG-
dc.contributor.nonIdAuthorPark, KK-
dc.contributor.nonIdAuthorYang, KH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorchlorophyllin-
dc.subject.keywordAuthornitric oxide-
dc.subject.keywordAuthorlipopolysaccharide-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusPERITONEAL-MACROPHAGES-
dc.subject.keywordPlusINHIBITS INDUCTION-
dc.subject.keywordPlusSYNTHASE GENE-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusPEROXYNITRITE CAUSES-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusINTERFERON-GAMMA-
dc.subject.keywordPlusDNA-BINDING-
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