Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Min-Seon | - |
dc.contributor.author | Park, Jin-Soo | - |
dc.contributor.author | Chung, You Chul | - |
dc.contributor.author | Jang, Sungchan | - |
dc.contributor.author | Hyun, Chang-Gu | - |
dc.contributor.author | Kim, Seung-Young | - |
dc.date.accessioned | 2024-01-19T19:00:44Z | - |
dc.date.available | 2024-01-19T19:00:44Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2019-11 | - |
dc.identifier.issn | 1420-3049 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/119362 | - |
dc.description.abstract | Biorenovation is a microbial enzyme-catalyzed structural modification of organic compounds with the potential benefits of reduced toxicity and improved biological properties relative to their precursor compounds. In this study, we synthesized a novel compound verified as formononetin 7-O-phosphate (FMP) from formononetin (FM) using microbial biotransformation. We further compared the anti-inflammatory properties of FMP to FM in lipopolysaccharide (LPS)-treated RAW264.7 macrophage cells. We observed that cell viabilities and inhibitory effects on LPS-induced nitric oxide (NO) production were greater in FMP-treated RAW 264.7 cells than in their FM-treated counterparts. In addition, FMP treatment suppressed the production of proinflammatory cytokines such as prostaglandin-E-2 (PGE(2)), interleukin-6 (IL-6), and interleukin-1 beta (IL-1 beta) in a dose-dependent manner and concomitantly decreased the mRNA expression of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2). We also found that FMP exerted its anti-inflammatory effects through the downregulation of the extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and nuclear factor kappa B (NF-kappa B) signaling pathways. In conclusion, we generated a novel anti-inflammatory compound using biorenovation and demonstrated its efficacy in cell-based in vitro assays. | - |
dc.language | English | - |
dc.publisher | MDPI | - |
dc.subject | KAPPA-B ACTIVATION | - |
dc.subject | NITRIC-OXIDE | - |
dc.subject | INDUCED INOS | - |
dc.subject | SIGNALING PATHWAYS | - |
dc.subject | INHIBITION | - |
dc.subject | EXPRESSION | - |
dc.subject | PHOSPHORYLATION | - |
dc.subject | INFLAMMATION | - |
dc.subject | COMPOUND | - |
dc.subject | VITRO | - |
dc.title | Anti-Inflammatory Effects of Formononetin 7-O-phosphate, a Novel Biorenovation Product, on LPS-Stimulated RAW 264.7 Macrophage Cells | - |
dc.type | Article | - |
dc.identifier.doi | 10.3390/molecules24213910 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | MOLECULES, v.24, no.21 | - |
dc.citation.title | MOLECULES | - |
dc.citation.volume | 24 | - |
dc.citation.number | 21 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000498055500099 | - |
dc.identifier.scopusid | 2-s2.0-85074404703 | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | KAPPA-B ACTIVATION | - |
dc.subject.keywordPlus | NITRIC-OXIDE | - |
dc.subject.keywordPlus | INDUCED INOS | - |
dc.subject.keywordPlus | SIGNALING PATHWAYS | - |
dc.subject.keywordPlus | INHIBITION | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | PHOSPHORYLATION | - |
dc.subject.keywordPlus | INFLAMMATION | - |
dc.subject.keywordPlus | COMPOUND | - |
dc.subject.keywordPlus | VITRO | - |
dc.subject.keywordAuthor | biorenovation | - |
dc.subject.keywordAuthor | formononetin 7-O-phosphate | - |
dc.subject.keywordAuthor | anti-inflammatory | - |
dc.subject.keywordAuthor | MAPK pathway | - |
dc.subject.keywordAuthor | NF-kappa B pathway | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.