Methyl p-hydroxycinnamate exerts anti-inflammatory effects in mouse models of lipopolysaccharide-induced ARDS = 급성호흡부전 마우스 모델에서 Methyl p-hydroxycinnamate의 보호 효과

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dc.contributor.authorSeong Man Kim-
dc.contributor.authorJae-Hong Min-
dc.contributor.authorJung Hee Kim-
dc.contributor.authorJinseon Choi-
dc.contributor.authorJin-Mi Park-
dc.contributor.authorJuhyun Lee-
dc.contributor.authorSoo Hyeon Goo-
dc.contributor.authorJae Hoon Oh-
dc.contributor.authorSeung-Ho Kim-
dc.contributor.authorW Chun-
dc.contributor.authorKyung-Seop Ahn-
dc.contributor.authorS Kang-
dc.contributor.authorJae-Won Lee-
dc.date.accessioned2021-12-03T15:30:14Z-
dc.date.available2021-12-03T15:30:14Z-
dc.date.issued2022-
dc.identifier.issn1791-2997-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/25075-
dc.description.abstractMethyl p-hydroxycinnamate (MH), an esterified derivative of p-Coumaric acid exerts anti-inflammatory effects on lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. Based on these effects, the present study investigated the protective role of MH in a mouse model of LPS-induced acute respiratory distress syndrome (ARDS). The results demonstrated that administration of LPS (5 mg/kg intranasally) markedly increased the neutrophil/macrophage numbers and levels of inflammatory molecules (TNF-α, IL-6, IL-1β and reactive oxygen species) in the bronchoalveolar lavage fluid (BALF) of mice. On histological examination, the presence of inflammatory cells was observed in the lungs of mice administered LPS. LPS also notably upregulated the secretion of monocyte chemoattractant protein-1 and protein content in BALF as well as expression of inducible nitric oxide synthase in the lungs of mice; it also caused activation of p38 mitogen-activated protein kinase (MAPK) and NF-κB signaling. However, MH treatment significantly suppressed LPS-induced upregulation of inflammatory cell recruitment, inflammatory molecule levels and p38MAPK/NF-κB activation, and also led to upregulation of heme oxygenase-1 (HO-1) expression in the lungs of mice. In addition, the ability of MH to induce HO-1 expression was confirmed in RAW264.7 macrophages. Taken together, the findings of the present study indicated that MH may exert protective effects against airway inflammation in ARDS mice by inhibiting inflammatory cell recruitment and the production of inflammatory molecules.-
dc.publisherSpandidos Publ Ltd-
dc.titleMethyl p-hydroxycinnamate exerts anti-inflammatory effects in mouse models of lipopolysaccharide-induced ARDS = 급성호흡부전 마우스 모델에서 Methyl p-hydroxycinnamate의 보호 효과-
dc.title.alternativeMethyl p-hydroxycinnamate exerts anti-inflammatory effects in mouse models of lipopolysaccharide-induced ARDS-
dc.typeArticle-
dc.citation.titleMolecular Medicine Reports-
dc.citation.number1-
dc.citation.endPage37-
dc.citation.startPage37-
dc.citation.volume25-
dc.contributor.affiliatedAuthorSeong Man Kim-
dc.contributor.affiliatedAuthorJae-Hong Min-
dc.contributor.affiliatedAuthorJung Hee Kim-
dc.contributor.affiliatedAuthorJinseon Choi-
dc.contributor.affiliatedAuthorJin-Mi Park-
dc.contributor.affiliatedAuthorJuhyun Lee-
dc.contributor.affiliatedAuthorSoo Hyeon Goo-
dc.contributor.affiliatedAuthorJae Hoon Oh-
dc.contributor.affiliatedAuthorSeung-Ho Kim-
dc.contributor.affiliatedAuthorKyung-Seop Ahn-
dc.contributor.affiliatedAuthorJae-Won Lee-
dc.contributor.alternativeName김성만-
dc.contributor.alternativeName민재홍-
dc.contributor.alternativeName김정희-
dc.contributor.alternativeName최진선-
dc.contributor.alternativeName박진미-
dc.contributor.alternativeName이주현-
dc.contributor.alternativeName구수현-
dc.contributor.alternativeName오재훈-
dc.contributor.alternativeName김승호-
dc.contributor.alternativeName전완주-
dc.contributor.alternativeName안경섭-
dc.contributor.alternativeName강석모-
dc.contributor.alternativeName이재원-
dc.identifier.bibliographicCitationMolecular Medicine Reports, vol. 25, no. 1, pp. 37-37-
dc.identifier.doi10.3892/mmr.2021.12553-
dc.subject.keywordAcute respiratory distress syndrome-
dc.subject.keywordMethyl p-hydroxycinnamate-
dc.subject.keywordInflammatory cell-
dc.subject.keywordNF-κB-
dc.subject.keywordHeme oxygenase-1-
dc.subject.localAcute respiratory distress syndrome-
dc.subject.localMethyl p-hydroxycinnamate-
dc.subject.localInflammatory cells-
dc.subject.localInflammatory cell-
dc.subject.localNuclear factor-kappa B-
dc.subject.localnuclear factor κB-
dc.subject.localNf-κb-
dc.subject.localNF-kB-
dc.subject.localnuclear factor kappa B-
dc.subject.localNF-κB (nuclear factor kappa-B)-
dc.subject.localNF-kappaB-
dc.subject.localNuclear factor-κb-
dc.subject.localNF-κ B-
dc.subject.localNF-κB-
dc.subject.localNF-kappa B-
dc.subject.localNuclear factor κB (NF-κB)-
dc.subject.localNuclear factor κB-
dc.subject.localNFκB-
dc.subject.localNf-κB-
dc.subject.localNuclear factor-κB-
dc.subject.localnuclear factorκB-
dc.subject.localNuclear factor (NF)-κB-
dc.subject.localNuclear factor kappa B-
dc.subject.localnuclear factor-κB-
dc.subject.localNF-ΚB-
dc.subject.localNuclear factor-kappa B (NF-κB)-
dc.subject.localNuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB (NF-κB)-
dc.subject.localNFkappaB-
dc.subject.localNuclear factor kappaB-
dc.subject.localHeme oxygenase-1-
dc.subject.localHeme-oxygenase 1-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Bio-Resource Central Bank > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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