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Anti-inflammatory, antinociceptive and anti-angiogenic activities of a phospholipid mixture purified from porcine lung tissues

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dc.contributor.authorJung, Hyun-Joo-
dc.contributor.authorMoon, Jeong-Su-
dc.contributor.authorPark, A. Rum-
dc.contributor.authorChoi, Hojin-
dc.contributor.authorLee, Jong Eun-
dc.contributor.authorChoi, Seong-Hyun-
dc.contributor.authorLim, Chang-Jin-
dc.date.accessioned2022-07-16T15:06:17Z-
dc.date.available2022-07-16T15:06:17Z-
dc.date.issued2012-06-
dc.identifier.issn0892-3973-
dc.identifier.issn1532-2513-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/165395-
dc.description.abstractThis work aimed to assess anti-inflammatory and related properties of a phospholipid mixture purified from porcine lung tissues, named KT&G101, which is being developed as a novel topical remedy for atopic dermatitis. KT&G101 consists of pure phospholipids, mainly phosphatidylcholine (PC) and other phospholipids such as phosphatidylinositol (PI) and phosphatidylserine (PS). Its predominant PC species is 1,2-dipalmitoylphosphatidylcholine (DPPC). KT&G101 exhibited an anti-angiogenic activity in the chick chorioallantoic membrane (CAM) assay. Oral administration of KT&G101 at the dosages of 100, 200 and 400 mg/kg body weight gave rise to an inhibition of 15.4%, 25.3% and 30.1% in the vascular permeability assay, respectively. In the carrageenan-induced inflammation in the air pouches, KT&G101 significantly diminished the volume of exudates in the pouches, the number of polymorphonuclear leukocytes and nitrite content in exudates. In the acetic acid-induced writhing response, oral administration of KT&G101 at the dosages of 50, 100 and 200 mg/kg body weight showed the reduction of 21.6%, 51.6% and 60.8% in the pain response of mice, respectively. It was also able to diminish the nitric oxide (NO) and reactive oxygen species (ROS) levels in the lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells. KT&G101 displayed a significant suppression on the induction of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in the stimulated RAW264.7 cells. However, the free radical scavenging activity of KT&G101 was detected to be very weak in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Taken together, KT&G101 possesses anti-inflammatory and related antinociceptive and anti-angiogenic activities, which indirectly supports its use as an anti-atopic therapy.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherMarcel Dekker Inc.-
dc.titleAnti-inflammatory, antinociceptive and anti-angiogenic activities of a phospholipid mixture purified from porcine lung tissues-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.3109/08923973.2011.611137-
dc.identifier.scopusid2-s2.0-84860718255-
dc.identifier.wosid000303830400007-
dc.identifier.bibliographicCitationImmunopharmacology and Immunotoxicology, v.34, no.3, pp 398 - 407-
dc.citation.titleImmunopharmacology and Immunotoxicology-
dc.citation.volume34-
dc.citation.number3-
dc.citation.startPage398-
dc.citation.endPage407-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusATOPIC-DERMATITIS-
dc.subject.keywordPlusNC/NGA MICE-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusPULMONARY SURFACTANT-
dc.subject.keywordPlusROSMARINIC ACID-
dc.subject.keywordPlusSKIN-LESIONS-
dc.subject.keywordPlusPHOSPHATIDYLCHOLINE-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorPhospholipid-
dc.subject.keywordAuthoranti-inflammatory-
dc.subject.keywordAuthorantinociceptive-
dc.subject.keywordAuthoranti-angiogenic-
dc.subject.keywordAuthorcyclooxygenase-2-
dc.subject.keywordAuthorinducible nitric oxide synthase-
dc.subject.keywordAuthornitric oxide-
dc.subject.keywordAuthorreactive oxygen species-
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.3109/08923973.2011.611137-
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