Alismol purified from the tuber of Alisma orientale relieves acute lung injury in mice via Nrf2 activation

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dc.contributor.authorK H Kim-
dc.contributor.authorS Kim-
dc.contributor.authorM J Kwun-
dc.contributor.authorJ Y Lee-
dc.contributor.authorSei-Ryang Oh-
dc.contributor.authorJ Y Choi-
dc.contributor.authorM Joo-
dc.date.accessioned2023-11-15T16:32:34Z-
dc.date.available2023-11-15T16:32:34Z-
dc.date.issued2023-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32976-
dc.description.abstractSince the ethanol extract of Alisma orientale Juzepzuk (EEAO) suppresses lung inflammation by suppressing Nuclear Factor-kappa B (NF-κB) and activating Nuclear Factor Erythroid 2-related Factor 2 (Nrf2), we set out to identify chemicals constituting EEAO that suppress lung inflammation. Here, we provide evidence that among the five most abundant chemical constituents identified by Ultra Performance Liquid Chromatography (UPLC) and Nuclear Magnetic Resonance (NMR), alismol is one of the candidate constituents that suppresses lung inflammation in a lipopolysaccharide (LPS)-induced acute lung injury (ALI) mouse model and protects mice from ALI-like symptoms. Alismol did not induce cytotoxicity or reactive oxygen species (ROS). When administered to the lung of LPS-induced ALI mice (n = 5/group), alismol decreased the level of neutrophils and of the pro-inflammatory molecules, including Tumor Necrosis Factor-alpha (TNF-α), Interleukin-1 beta (IL-1β), Interleukin-6 (IL-6), Monocyte Chemoattractant Protein-1 (MCP-1), Interferon-gamma (IFN-γ), and Cyclooxygenase-2 (COX-2), suggesting an anti-inflammatory activity of alismol. Consistent with these findings, alismol ameliorated the key features of the inflamed lung of ALI, such as high cellularity due to infiltrated inflammatory cells, the development of hyaline membrane structure, and capillary destruction. Unlike EEAO, alismol did not suppress NF-κB activity but rather activated Nrf2. Consequently, alismol induced the expression of prototypic genes regulated by Nrf2, including Heme Oxygenase-1 (HO-1), NAD(P)H: quinine oxidoreductase-1 (NQO-1), and glutamyl cysteine ligase catalytic units (GCLC). Alismol activating Nrf2 appears to be associated with a decrease in the ubiquitination of Nrf2, a key suppressive mechanism for Nrf2 activity. Together, our results suggest that alismol is a chemical constituent of EEAO that contributes at least in part to suppressing some of the key features of ALI by activating Nrf2.-
dc.publisherMDPI-
dc.titleAlismol purified from the tuber of Alisma orientale relieves acute lung injury in mice via Nrf2 activation-
dc.title.alternativeAlismol purified from the tuber of Alisma orientale relieves acute lung injury in mice via Nrf2 activation-
dc.typeArticle-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.number21-
dc.citation.endPage15573-
dc.citation.startPage15573-
dc.citation.volume24-
dc.contributor.affiliatedAuthorSei-Ryang Oh-
dc.contributor.alternativeName김균하-
dc.contributor.alternativeName김소연-
dc.contributor.alternativeName권민정-
dc.contributor.alternativeName이지연-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName최준용-
dc.contributor.alternativeName주명수-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, vol. 24, no. 21, pp. 15573-15573-
dc.identifier.doi10.3390/ijms242115573-
dc.subject.keywordAcute lung injury-
dc.subject.keywordAlismol-
dc.subject.keywordAlisma orientale Juzepzuk-
dc.subject.keywordMouse model-
dc.subject.keywordNeutrophilic lung inflammation-
dc.subject.keywordNF-κB-
dc.subject.keywordNrf2-
dc.subject.localAcute Lung Injury-
dc.subject.localAcute lung injury-
dc.subject.localacute lung injury-
dc.subject.localacute lung injury (ALI)-
dc.subject.localMouse model-
dc.subject.localmouse model-
dc.subject.localNeutrophilic lung inflammation-
dc.subject.localNFkappaB-
dc.subject.localNFκB-
dc.subject.localNf-κB-
dc.subject.localNf-κb-
dc.subject.localNuclear factor (NF)-κB-
dc.subject.localNuclear factor kappa B-
dc.subject.localNuclear factor kappaB-
dc.subject.localNuclear factor κB-
dc.subject.localNuclear factor κB (NF-κB)-
dc.subject.localNuclear factor-kappa B-
dc.subject.localNuclear factor-kappa B (NF-κB)-
dc.subject.localNuclear factor-kappaB-
dc.subject.localNuclear factor-κB-
dc.subject.localNuclear factor-κb-
dc.subject.localNF-kB-
dc.subject.localNF-kappa B-
dc.subject.localNF-kappaB-
dc.subject.localNF-ΚB-
dc.subject.localNF-κ B-
dc.subject.localNF-κB-
dc.subject.localNF-κB (nuclear factor kappa-B)-
dc.subject.localnuclear factor kappa B-
dc.subject.localnuclear factor κB-
dc.subject.localnuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB (NF-κB)-
dc.subject.localnuclear factor-κB-
dc.subject.localnuclear factorκB-
dc.subject.localNRF2-
dc.subject.localNrf-2-
dc.subject.localNrf2-
dc.description.journalClassY-
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Ochang Branch Institute > 1. Journal Articles
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