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Callerya atropurpurea suppresses inflammation in vitro and ameliorates gastric injury as well as septic shock in vivo via TLR4/MyD88-dependent cascade

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dc.contributor.authorYou, Long-
dc.contributor.authorHuang, Lei-
dc.contributor.authorJang, Jiwon-
dc.contributor.authorHong, Yo Han-
dc.contributor.authorKim, Han Gyung-
dc.contributor.authorChen, Hongxi-
dc.contributor.authorShin, Chae Yun-
dc.contributor.authorYoon, Ji Hye-
dc.contributor.authorManilack, Philaxay-
dc.contributor.authorSounyvong, Bounthan-
dc.contributor.authorLee, Woo-Shin-
dc.contributor.authorJeon, Mi-Jeong-
dc.contributor.authorLee, Sarah-
dc.contributor.authorLee, Byoung-Hee-
dc.contributor.authorCho, Jae Youl-
dc.date.accessioned2022-10-11T00:27:52Z-
dc.date.available2022-10-11T00:27:52Z-
dc.date.created2022-09-29-
dc.date.issued2022-10-
dc.identifier.citationPhytomedicine, Vol.105, p. 154338-
dc.identifier.issn0944-7113-
dc.identifier.urihttps://hdl.handle.net/10371/185651-
dc.description.abstract© 2022Background: Callerya atropurpurea is a traditional plant in a tropical zone discovered to have anti-inflammatory functions. Purpose: we want to investigate the mechanism related to anti-inflammation of C. atropurpurea ethanol extract (Ca-EE) both in vitro and in vivo. Study design: Murine macrophage cells and mouse models for gastritis and septic shock were conducted to evaluate the abilities of Ca-EE in anti-inflammation. Methods: Ca-EE was tested by HPLC and LC-MS/MS. NO outcome was checked by Griess reagent test. Cell viabilities were evaluated using MTT assay. Inflammatory cytokines were determined via RT-PCR and ELISA. The mechanism of Ca-EE in anti-inflammation was investigated by luciferase reporter gene assay and immunoblot in transcription level and protein level respectively. Gastric injury and septic shock administrated with Ca-EE were studied by H&E, PCR, and immunoblot. Results: Ca-EE significantly decreased LPS-induced NO production, but hardly stimulated the expression of NO itself. It not only showed no cytotoxicity, but also protected cells from LPS damage. Moreover, Ca-EE decreased TLR4 expression, altered MyD88 recruitment and TRAF6, and suppressed the phospho-Src/PI3K/AKT. Ca-EE inhibited downstream signaling P38, JNK and NF-κB. Finally, Ca-EE alleviated HCl/EtOH-induced gastritis and LPS/poly (I:C)-induced septic shock through the previously mentioned signaling cascades. Conclusion: Ca-EE exhibited an integrated and promising mechanism against TLR4-related inflammation, which shows potential for treating gastritis, septic shock, and other inflammatory diseases.-
dc.language영어-
dc.publisherElsevier GmbH-
dc.titleCallerya atropurpurea suppresses inflammation in vitro and ameliorates gastric injury as well as septic shock in vivo via TLR4/MyD88-dependent cascade-
dc.typeArticle-
dc.identifier.doi10.1016/j.phymed.2022.154338-
dc.citation.journaltitlePhytomedicine-
dc.identifier.scopusid2-s2.0-85135507548-
dc.citation.startpage154338-
dc.citation.volume105-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorLee, Woo-Shin-
dc.type.docTypeArticle-
dc.description.journalClass1-
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