Ponciri Fructus Immaturus ethanol extract attenuates septic shock through inhibition of the STAT1 signaling pathway

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dc.contributor.authorYo Sep Hwang-
dc.contributor.authorJun-Pil Jang-
dc.contributor.authorS H Park-
dc.contributor.authorA Kim-
dc.contributor.authorJae-Hyuk Jang-
dc.contributor.authorHyang Ran Yoon-
dc.contributor.authorSuk Ran Yoon-
dc.contributor.authorJ H Park-
dc.contributor.authorHee Jun Cho-
dc.contributor.authorHee Gu Lee-
dc.date.accessioned2022-09-29T16:32:38Z-
dc.date.available2022-09-29T16:32:38Z-
dc.date.issued2022-
dc.identifier.issn2296-861X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/30395-
dc.description.abstractSepsis is a systemic inflammatory disease to infections and results in tissue damage and multiple organ failure. Ponciri Fructus Immaturus (PFI) is widely used in traditional medicine for allergic inflammation and gastrointestinal disorders. However, the effect of PFI on sepsis is still unknown. This study investigated the anti-inflammatory and antiseptic effects of PFI ethanol extract (PFIE) in LPS-stimulated J774 macrophages and mice with CLP- or LPSinduced sepsis, respectively. PFIE attenuates the LPS-induced production of the proinflammatory mediator NO by inhibiting the expression of iNOS in J774 cells. Real-time RT-PCR data and ELISA showed that the mRNA and protein levels of TNF-a, IL-1b, and IL-6 increased in LPS-stimulated J774 cells. However, this induction was significantly suppressed in PFIE pre-treated J774 cells. We also found that PFIE administration increased the survival rate of mice with LPS- and CLP-induced sepsis. Decreased serum levels of AST, ALT, and CK were observed after administration of PFIE, which was associated with reduced production of proinflammatory factors, such as NO, TNF-a, IL-1b, and IL-6. Moreover, PFIE suppressed the phosphorylation and nuclear translocation of STAT1 in LPS-stimulated J774 cells, suggesting that PFIE can inhibit LPS- and CLP-induced septic shock by suppressing the STAT1 activation. These findings provide the potential therapeutic relevance of PFIE in treating acute inflammatory disease.-
dc.publisherFrontiers Media Sa-
dc.titlePonciri Fructus Immaturus ethanol extract attenuates septic shock through inhibition of the STAT1 signaling pathway-
dc.title.alternativePonciri Fructus Immaturus ethanol extract attenuates septic shock through inhibition of the STAT1 signaling pathway-
dc.typeArticle-
dc.citation.titleFrontiers in Nutrition-
dc.citation.number0-
dc.citation.endPage988309-
dc.citation.startPage988309-
dc.citation.volume9-
dc.contributor.affiliatedAuthorYo Sep Hwang-
dc.contributor.affiliatedAuthorJun-Pil Jang-
dc.contributor.affiliatedAuthorJae-Hyuk Jang-
dc.contributor.affiliatedAuthorHyang Ran Yoon-
dc.contributor.affiliatedAuthorSuk Ran Yoon-
dc.contributor.affiliatedAuthorHee Jun Cho-
dc.contributor.affiliatedAuthorHee Gu Lee-
dc.contributor.alternativeName황요셉-
dc.contributor.alternativeName장준필-
dc.contributor.alternativeName박성훈-
dc.contributor.alternativeName김애영-
dc.contributor.alternativeName장재혁-
dc.contributor.alternativeName윤향란-
dc.contributor.alternativeName윤석란-
dc.contributor.alternativeName박준홍-
dc.contributor.alternativeName조희준-
dc.contributor.alternativeName이희구-
dc.identifier.bibliographicCitationFrontiers in Nutrition, vol. 9, pp. 988309-988309-
dc.identifier.doi10.3389/fnut.2022.988309-
dc.subject.keywordPonciri Fructus Immaturus-
dc.subject.keywordSepsis-
dc.subject.keywordInflammation-
dc.subject.keywordPro-inflammatory cytokines-
dc.subject.keywordSTAT1-
dc.subject.localsepsis-
dc.subject.localSepsis-
dc.subject.localInflammation-
dc.subject.localinflammation-
dc.subject.localPro-inflammatory cytokine-
dc.subject.localPro-inflammatory cytokines-
dc.subject.localProinflammatory cytokine-
dc.subject.localProinflammatory cytokines-
dc.subject.localpro-inflammatory cytokine-
dc.subject.localproinflammatory cytokine-
dc.subject.localSTAT-1-
dc.subject.localSTAT1-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
Division of Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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