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Activation of melatonin receptor 1 by CRISPR-Cas9 activator ameliorates cognitive deficits in an Alzheimer's disease mouse model

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dc.contributor.authorPark, Hanseul-
dc.contributor.authorKim, Jongpil-
dc.date.accessioned2023-04-27T12:40:39Z-
dc.date.available2023-04-27T12:40:39Z-
dc.date.issued2022-04-
dc.identifier.issn0742-3098-
dc.identifier.issn1600-079X-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/3402-
dc.description.abstractAlzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the presence of neurotoxic beta-amyloid (A beta) in the brain. Melatonin receptors have been reported to associate with aging and AD, and their expression decreased with the progression of AD. As an alternative to AD treatment, overexpression of melatonin receptors may lead to melatonin-like effects to treat alleviate the symptoms of AD. Here, we successfully activated the type 1 melatonin receptor (Mt1) in vivo brain using a Cas9 activator as a novel AD therapeutic strategy. The Cas9 activator efficiently activated the endogenous Mt1 gene in the brain. Activation of Mt1 via Cas9 activators modulated anti-amyloidogenic and anti-inflammatory roles in 5xFAD AD mice brain. Moreover, activation of Mt1 with the CRISPR/Cas9 activator improved cognitive deficits in an AD model. These results demonstrated the therapeutic potential of melatonin receptor activation via CRISPR/Cas9 activator for AD.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleActivation of melatonin receptor 1 by CRISPR-Cas9 activator ameliorates cognitive deficits in an Alzheimer's disease mouse model-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/jpi.12787-
dc.identifier.scopusid2-s2.0-85126223681-
dc.identifier.wosid000768321000001-
dc.identifier.bibliographicCitationJournal of Pineal Research, v.72, no.3, pp 1 - 14-
dc.citation.titleJournal of Pineal Research-
dc.citation.volume72-
dc.citation.number3-
dc.citation.startPage1-
dc.citation.endPage14-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusTRAUMATIC BRAIN-INJURY-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusSUPRACHIASMATIC NUCLEUS-
dc.subject.keywordPlusTRANSCRIPTIONAL ACTIVATION-
dc.subject.keywordPlusCEREBROSPINAL-FLUID-
dc.subject.keywordPlusMEMORY IMPAIRMENT-
dc.subject.keywordPlusMT1 RECEPTOR-
dc.subject.keywordPlusDRUG-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordAuthorAlzheimer's disease-
dc.subject.keywordAuthorCas9 activator-
dc.subject.keywordAuthormelatonin receptor-
dc.subject.keywordAuthorMt1-
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