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Novel benzofuran derivative DK-1014 attenuates lung inflammation via blocking of MAPK/AP-1 and AKT/mTOR signaling in vitro and in vivo

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dc.contributor.authorXu, Xuezhen-
dc.contributor.authorKwon, Ok-Kyoung-
dc.contributor.authorShin, In-Sik-
dc.contributor.authorMali, Jyotirling R.-
dc.contributor.authorHarmalkar, Dipesh S.-
dc.contributor.authorLim, Yourim-
dc.contributor.authorLee, Gilhye-
dc.contributor.authorLu, Qili-
dc.contributor.authorOh, Sei-Ryang-
dc.contributor.authorAhn, Kyung-Seop-
dc.contributor.authorJeong, Hye-Gwang-
dc.contributor.authorLee, Kyeong-
dc.date.accessioned2023-04-28T05:41:19Z-
dc.date.available2023-04-28T05:41:19Z-
dc.date.issued2019-01-29-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/8475-
dc.description.abstractBenzofuran derivatives have wide range of biological activities as anti-oxidant, anti-inflammatory and anticonvulsant agent. In this study, we investigated whether the novel benzofuran derivative, DK-1014 has the anti-inflammatory effects on macrophage and lung epithelial cells and anti-asthmatic effects on ovalbumin-treated mice. A series of 2-arylbenzofuran analogues were synthesized and evaluated for NO and interleukin-6 (IL-6) inhibition in LPS-stimulated Raw264.7 cells. Of these analogues, compounds 8, 22a, 22d, and 22 f (DK-1014) exhibited notable inhibitory activity with respect to IL-6 and NO production. In particular, compound DK-1014 strongly reduced IL-6, IL-8, and MMP-9 mRNA expression and IL-6, IL-8, and MCP-1 production in phorbol myristate acetate stimulated A549 cells, reduced MAPKs phosphorylation and c-fos translocation, and attenuated AKT, p70S6K and GSK phosphorylation. In vivo experiments were also performed on ovalbumin-sensitized and challenged BALB/c mice. DK-1014 reduced the airway hyperresponsiveness, inflammatory cell counts and cytokine levels (IL-4, 5, 13) in bronchial alveolar lavage fluid (BALF) and immunoglobulin E in serum, and attenuated inflammatory cell infiltration and mucus hypersecretion in lung tissue. These findings indicate that DK-1014 can protect against allergic airway inflammation through the AP-1 and AKT/ mTOR pathways and could be useful source for the development of a therapeutic agent for asthma.-
dc.language영어-
dc.language.isoENG-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleNovel benzofuran derivative DK-1014 attenuates lung inflammation via blocking of MAPK/AP-1 and AKT/mTOR signaling in vitro and in vivo-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1038/s41598-018-36925-9-
dc.identifier.scopusid2-s2.0-85060785919-
dc.identifier.wosid000456955500042-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.9, no.1-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume9-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusAIRWAY INFLAMMATION-
dc.subject.keywordPlusREGULATED KINASE-
dc.subject.keywordPlusLIPOPOLYSACCHARIDE-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusAP-1-
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