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DC FieldValueLanguage
dc.contributor.author이상경-
dc.date.accessioned2019-12-09T18:19:54Z-
dc.date.available2019-12-09T18:19:54Z-
dc.date.issued2018-10-
dc.identifier.citationSCIENTIFIC REPORTS, v. 8, Article no. 15041en_US
dc.identifier.issn2045-2322-
dc.identifier.urihttps://www.nature.com/articles/s41598-018-33296-z-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/120338-
dc.description.abstractIschemic stroke-induced neuronal cell death results in the permanent disabling of brain function. Apoptotic mechanisms are thought to play a prominent role in neuronal injury and ample evidence implicates Fas signaling in mediating cell death. In this study, we describe the neuroprotective effects of a Fas-blocking peptide (FBP) that by obstructing Fas signaling in cerebral ischemia inhibits apoptosis. Using an intranasal administration route in a rat model of focal cerebral ischemia, we demonstrate that nose-to-brain delivery of FBP after middle cerebral artery occlusion (MCAO) surgery results in the delivery and retention of FBP in Fas-expressing ischemic areas of the brain. A single intranasal administration of 2 mg/kg FBP resulted in significantly reduced neuronal cell death by inhibiting Fas-mediated apoptosis leading to decreased infarct volumes, reduced neurologic deficit scores and recovery from cerebral ischemia. Intranasally delivered FBP might be a promising strategy for the treatment of cerebral ischemic stroke.en_US
dc.description.sponsorshipThis work was supported by NIH grant R01AI112443 to P.K. and the Korea National Research. Foundation grant 2017R1D1A1B03029636 and 2018R1D1A1B07050464 to S.K.L.en_US
dc.language.isoen_USen_US
dc.publisherNATURE PUBLISHING GROUPen_US
dc.subjectNASAL DRUG-DELIVERYen_US
dc.subjectGLUCOSE-TRANSPORTERen_US
dc.subjectSTROKEen_US
dc.subjectMECHANISMSen_US
dc.subjectBARRIERen_US
dc.subjectTARGETen_US
dc.subjectSIRNAen_US
dc.subjectCELLen_US
dc.subjectMEMBRANESen_US
dc.subjectNECROSISen_US
dc.titleIntranasal delivery of a Fas-blocking peptide attenuates Fas-mediated apoptosis in brain ischemiaen_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume8-
dc.identifier.doi10.1038/s41598-018-33296-z-
dc.relation.page1-10-
dc.relation.journalSCIENTIFIC REPORTS-
dc.contributor.googleauthorUllah, Irfan-
dc.contributor.googleauthorChung, Kunho-
dc.contributor.googleauthorOh, Jungju-
dc.contributor.googleauthorBeloor, Jagadish-
dc.contributor.googleauthorBae, Sumin-
dc.contributor.googleauthorLee, Sangah Clara-
dc.contributor.googleauthorLee, Minhyung-
dc.contributor.googleauthorKumar, Priti-
dc.contributor.googleauthorLee, Sang-Kyung-
dc.relation.code2018003596-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF BIOENGINEERING-
dc.identifier.pidsangkyunglee-


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