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dc.contributor.authorIshikawa, T-
dc.contributor.authorKaneko, M-
dc.contributor.authorShin, HS-
dc.contributor.authorTakahashi, T-
dc.date.accessioned2024-01-21T04:10:35Z-
dc.date.available2024-01-21T04:10:35Z-
dc.date.created2021-09-03-
dc.date.issued2005-10-01-
dc.identifier.issn0022-3751-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136061-
dc.description.abstractAt the nerve terminal, both N- and P/Q-type Ca2+ channels mediate synaptic transmission, with their relative contribution varying between synapses and with postnatal age. To clarify functional significance of different presynaptic Ca2+ channel subtypes, we recorded N-type and P/Q-type Ca2+ currents directly from calyces of Held nerve terminals in alpha(1A)-subunit-deficient mice and wild-type (WT) mice, respectively. The most prominent feature of P/Q-type Ca2+ currents was activity-dependent facilitation, which was absent for N-type Ca2+ currents. EPSCs mediated by P/Q-type Ca2+ currents showed less depression during high-frequency stimulation compared with those mediated by N-type Ca2+ currents. In addition, the maximal inhibition by the GABA(B) receptor agonist baclofen was greater for EPSCs mediated by N-type channels than for those mediated by P/0-type channels. These results suggest that the developmental switch of presynaptic Ca2+ channels from N- to P/Q-type may serve to increase synaptic efficacy at high frequencies of activity, securing high-fidelity synaptic transmission.-
dc.languageEnglish-
dc.publisherWILEY-
dc.subjectSHORT-TERM DEPRESSION-
dc.subjectGTP-BINDING PROTEIN-
dc.subjectCALCIUM-CHANNELS-
dc.subjectTRANSMITTER RELEASE-
dc.subjectDEVELOPMENTAL-CHANGES-
dc.subjectADENOSINE A(1)-
dc.subjectCURRENTS-
dc.subjectFACILITATION-
dc.subjectINHIBITION-
dc.subjectMODULATION-
dc.titlePresynaptic N-type and P/Q-type Ca2+ channels mediating synaptic transmission at the calyx of held of mice-
dc.typeArticle-
dc.identifier.doi10.1113/jphysiol.2005.089912-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF PHYSIOLOGY-LONDON, v.568, no.1, pp.199 - 209-
dc.citation.titleJOURNAL OF PHYSIOLOGY-LONDON-
dc.citation.volume568-
dc.citation.number1-
dc.citation.startPage199-
dc.citation.endPage209-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000232474900018-
dc.identifier.scopusid2-s2.0-26844476796-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPhysiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusSHORT-TERM DEPRESSION-
dc.subject.keywordPlusGTP-BINDING PROTEIN-
dc.subject.keywordPlusCALCIUM-CHANNELS-
dc.subject.keywordPlusTRANSMITTER RELEASE-
dc.subject.keywordPlusDEVELOPMENTAL-CHANGES-
dc.subject.keywordPlusADENOSINE A(1)-
dc.subject.keywordPlusCURRENTS-
dc.subject.keywordPlusFACILITATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusMODULATION-
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