Heterogeneity of tremor mechanisms assessed by tremor-related cortical potential in mice

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dc.contributor.authorPark, Young-Gyunko
dc.contributor.authorChoi, Jee Hyunko
dc.contributor.authorLee, Chungkiko
dc.contributor.authorKim, Sehyunko
dc.contributor.authorKim, Young Sooko
dc.contributor.authorChang, Ki-Youngko
dc.contributor.authorPaek, Sun Hako
dc.contributor.authorKim, Daesooko
dc.date.accessioned2015-04-07T05:16:51Z-
dc.date.available2015-04-07T05:16:51Z-
dc.date.created2015-02-26-
dc.date.created2015-02-26-
dc.date.created2015-02-26-
dc.date.issued2015-01-
dc.identifier.citationMOLECULAR BRAIN, v.8-
dc.identifier.issn1756-6606-
dc.identifier.urihttp://hdl.handle.net/10203/195325-
dc.description.abstractBackground: Identifying a neural circuit mechanism that is differentially involved in tremor would aid in the diagnosis and cure of such cases. Here, we demonstrate that tremor-related cortical potential (TRCP) is differentially expressed in two different mouse models of tremor. Results: Hybrid tremor analysis of harmaline-induced and genetic tremor in mice revealed that two authentic tremor frequencies for each type of tremor were conserved and showed an opposite dependence on CaV3.1 T-type Ca2+ channels. Electroencephalogram recordings revealed that a1(-/-); a1G(-/-) mice double-null for the GABA receptor a1 subunit (Gabra1) and CaV3.1 T-type Ca2+ channels (Cacna1g), in which the tremor caused by the absence of Gabra1 is potentiated by the absence of Cacna1g, showed a coherent TRCP that exhibited an onset that preceded the initiation of behavioral tremor by 3 ms. However, harmaline-induced tremor, which is known to be abolished by a1G(-/-), showed no TRCP. Conclusions: Our results demonstrate that the a1(-/-); a1G(-/-) double-knockout tremor model is useful for studying cortical mechanisms of tremor.-
dc.languageEnglish-
dc.publisherBIOMED CENTRAL LTD-
dc.titleHeterogeneity of tremor mechanisms assessed by tremor-related cortical potential in mice-
dc.typeArticle-
dc.identifier.wosid000348233900001-
dc.identifier.scopusid2-s2.0-85017331046-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.publicationnameMOLECULAR BRAIN-
dc.identifier.doi10.1186/s13041-015-0093-2-
dc.contributor.localauthorPark, Young-Gyun-
dc.contributor.localauthorKim, Daesoo-
dc.contributor.nonIdAuthorChoi, Jee Hyun-
dc.contributor.nonIdAuthorLee, Chungki-
dc.contributor.nonIdAuthorPaek, Sun Ha-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorTremor mechanism-
dc.subject.keywordAuthorCortical rhythm-
dc.subject.keywordAuthorHarmaline-
dc.subject.keywordAuthorT-type Ca2+ channels-
dc.subject.keywordPlusHARMALINE-INDUCED TREMOR-
dc.subject.keywordPlusMOTOR COORDINATION-
dc.subject.keywordPlusINFERIOR OLIVE-
dc.subject.keywordPlusCA2+ CHANNELS-
dc.subject.keywordPlusPATHOPHYSIOLOGY-
dc.subject.keywordPlusDISORDER-
dc.subject.keywordPlusCA(V)3.1-
dc.subject.keywordPlusNEURONS-
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