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Please use this identifier to cite or link to this item: https://scholars.tari.gov.tw/handle/123456789/19392
DC FieldValueLanguage
dc.contributor.authorHou-I Leeen_US
dc.contributor.authorJia-Hsin Guoen_US
dc.contributor.authorChih-Chung Wuen_US
dc.contributor.authorMao-Chang Tien_US
dc.contributor.authorKuang-Ping Lanen_US
dc.contributor.authorChun-Yi Huen_US
dc.contributor.authorChih-Yong Loen_US
dc.contributor.authorChi-Ching Yangen_US
dc.contributor.authorYaw-Feng Linen_US
dc.contributor.authorTzu-Ching Wangen_US
dc.date.accessioned2023-04-07T07:28:32Z-
dc.date.available2023-04-07T07:28:32Z-
dc.date.issued2011-04-
dc.identifier.issn1388-0209-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.3109/13880209.2010.517538-
dc.identifier.urihttps://scholars.tari.gov.tw/handle/123456789/19392-
dc.description.abstractObjective: In the present study, we investigated the anti-inflammatory effect of C. taiwanianum T. Yamaza rhizome aqueous extract (CTAE). Materials and methods: The present study investigated the anti-inflammatory effect of CTAE using IL-1 beta beta-induced NRK-52E cells. Production of NO and PGE(2) by ELISA, the mRNA and protein expression of iNOS and COX-2, phosphorylation of I kappa kappa B alpha alpha, and activation of NF-kappa kappa B by RT-PCR and western blotting were determined. Results: The CTAE significantly (P < 0.05) inhibited NO and PGE(2) production (decreased by 46.1% and 51%, respectively), and also significantly (P < 0.05) attenuated protein and mRNA expression of iNOS and COX-2 (decreased by 90% and 55% for iNOS and by 72% and 74%% for COX-2, respectively) in IL-1 beta beta-induced NRK-52E cells, in a dose-dependent manner, without obvious cytotoxic effects. Furthermore, the CTAE suppressed the NF-kappa kappa B nuclear translocation, in terms of inhibition of I kappa kappa B alpha alpha phosphorylation. Discussion and conclusion: Our results provided evidence for its folkloric uses and suggest that the anti-inflammatory activities of CTAE may result from the inhibition of inflammatory mediators, such as NO and PGE(2), and an upstream suppression of a NF-kappa kappa B-dependent mechanism, might be involved.en_US
dc.language.isoen_USen_US
dc.publisherTylor & Francis Ltd.en_US
dc.relation.ispartofPharmaceutical Biologyen_US
dc.subjectCynanchum taiwanianum T. Yamazaen_US
dc.subjectanti-inflammatory effecten_US
dc.subjectcyclooxygenase-2en_US
dc.subjectnitric oxide synthaseen_US
dc.subjectnuclear factor-kappa Ben_US
dc.titleAnti-inflammatory effects of Cynanchum taiwanianum rhizome aqueous extract in IL-1 beta beta-induced NRK-52E cellsen_US
dc.typejournal articleen_US
dc.identifier.doi10.3109/13880209.2010.517538-
dc.identifier.pmid21388234-
dc.identifier.isi000288758100016-
dc.relation.journalvolume49en_US
dc.relation.journalissue4en_US
dc.relation.pages437-444en_US
item.openairetypejournal article-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.languageiso639-1en_US-
item.fulltextno fulltext-
item.grantfulltextnone-
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