Isorhamnetin Protects Human Keratinocytes against Ultraviolet B-Induced Cell Damage

Cited 7 time in webofscience Cited 5 time in scopus
  • Hit : 393
  • Download : 0
DC FieldValueLanguage
dc.contributor.authorHan, Xiako
dc.contributor.authorPiao, Mei Jingko
dc.contributor.authorKim, Ki Cheonko
dc.contributor.authorHewage, Susara Ruwan Kumara Maddumako
dc.contributor.authorYoo, Eun Sookko
dc.contributor.authorKoh, Young Sangko
dc.contributor.authorKang, Hee Kyoungko
dc.contributor.authorShin, Jennifer Hyunjongko
dc.contributor.authorPark, Yeunsooko
dc.contributor.authorYoo, Suk Jaeko
dc.contributor.authorChae, Sko
dc.contributor.authorHyun, Jin Wonko
dc.date.accessioned2015-11-20T07:29:02Z-
dc.date.available2015-11-20T07:29:02Z-
dc.date.created2015-08-03-
dc.date.created2015-08-03-
dc.date.created2015-08-03-
dc.date.issued2015-07-
dc.identifier.citationBIOMOLECULES & THERAPEUTICS, v.23, no.4, pp.357 - 366-
dc.identifier.issn1976-9148-
dc.identifier.urihttp://hdl.handle.net/10203/200695-
dc.description.abstractIsorhamnetin (3-methylquercetin) is a flavonoid derived from the fruits of certain medicinal plants. This study investigated the photoprotective properties of isorhamnetin against cell damage and apoptosis resulting from excessive ultraviolet (UV) B exposure in human HaCaT keratinocytes. Isorhamnetin eliminated UVB-induced intracellular reactive oxygen species (ROS) and attenuated the oxidative modification of DNA, lipids, and proteins in response to UVB radiation. Moreover, isorhamnetin repressed UVB-facilitated programmed cell death in the keratinocytes, as evidenced by a reduction in apoptotic body formation, and nuclear fragmentation. Additionally, isorhamnetin suppressed the ability of UVB light to trigger mitochondrial dysfunction. Taken together, these results indicate that isorhamnetin has the potential to protect human keratinocytes against UVB-induced cell damage and death.-
dc.languageEnglish-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.titleIsorhamnetin Protects Human Keratinocytes against Ultraviolet B-Induced Cell Damage-
dc.typeArticle-
dc.identifier.wosid000357441700009-
dc.identifier.scopusid2-s2.0-84934278437-
dc.type.rimsART-
dc.citation.volume23-
dc.citation.issue4-
dc.citation.beginningpage357-
dc.citation.endingpage366-
dc.citation.publicationnameBIOMOLECULES & THERAPEUTICS-
dc.identifier.doi10.4062/biomolther.2015.005-
dc.contributor.localauthorShin, Jennifer Hyunjong-
dc.contributor.nonIdAuthorHan, Xia-
dc.contributor.nonIdAuthorPiao, Mei Jing-
dc.contributor.nonIdAuthorKim, Ki Cheon-
dc.contributor.nonIdAuthorHewage, Susara Ruwan Kumara Madduma-
dc.contributor.nonIdAuthorYoo, Eun Sook-
dc.contributor.nonIdAuthorKoh, Young Sang-
dc.contributor.nonIdAuthorKang, Hee Kyoung-
dc.contributor.nonIdAuthorPark, Yeunsoo-
dc.contributor.nonIdAuthorYoo, Suk Jae-
dc.contributor.nonIdAuthorChae, S-
dc.contributor.nonIdAuthorHyun, Jin Won-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorIsorhamnetin-
dc.subject.keywordAuthorUltraviolet B-
dc.subject.keywordAuthorReactive oxygen species-
dc.subject.keywordAuthorHuman keratinocyte-
dc.subject.keywordAuthorProgrammed cell death-
dc.subject.keywordPlusINDUCED OXIDATIVE STRESS-
dc.subject.keywordPlusHUMAN DERMAL FIBROBLAST-
dc.subject.keywordPlusINDUCED DNA-DAMAGE-
dc.subject.keywordPlusSCAVENGING ACTIVITY-
dc.subject.keywordPlusINDUCED-APOPTOSIS-
dc.subject.keywordPlusUVB IRRADIATION-
dc.subject.keywordPlusMITOCHONDRIAL-FUNCTION-
dc.subject.keywordPlusSTRAND BREAKS-
dc.subject.keywordPlusRADIATION-
dc.subject.keywordPlusSKIN-
Appears in Collection
ME-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 7 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0