Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Ishikawa, T | - |
dc.contributor.author | Kaneko, M | - |
dc.contributor.author | Shin, HS | - |
dc.contributor.author | Takahashi, T | - |
dc.date.accessioned | 2024-01-21T04:10:35Z | - |
dc.date.available | 2024-01-21T04:10:35Z | - |
dc.date.created | 2021-09-03 | - |
dc.date.issued | 2005-10-01 | - |
dc.identifier.issn | 0022-3751 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/136061 | - |
dc.description.abstract | At 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.language | English | - |
dc.publisher | WILEY | - |
dc.subject | SHORT-TERM DEPRESSION | - |
dc.subject | GTP-BINDING PROTEIN | - |
dc.subject | CALCIUM-CHANNELS | - |
dc.subject | TRANSMITTER RELEASE | - |
dc.subject | DEVELOPMENTAL-CHANGES | - |
dc.subject | ADENOSINE A(1) | - |
dc.subject | CURRENTS | - |
dc.subject | FACILITATION | - |
dc.subject | INHIBITION | - |
dc.subject | MODULATION | - |
dc.title | Presynaptic N-type and P/Q-type Ca2+ channels mediating synaptic transmission at the calyx of held of mice | - |
dc.type | Article | - |
dc.identifier.doi | 10.1113/jphysiol.2005.089912 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF PHYSIOLOGY-LONDON, v.568, no.1, pp.199 - 209 | - |
dc.citation.title | JOURNAL OF PHYSIOLOGY-LONDON | - |
dc.citation.volume | 568 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 199 | - |
dc.citation.endPage | 209 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000232474900018 | - |
dc.identifier.scopusid | 2-s2.0-26844476796 | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.relation.journalWebOfScienceCategory | Physiology | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalResearchArea | Physiology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SHORT-TERM DEPRESSION | - |
dc.subject.keywordPlus | GTP-BINDING PROTEIN | - |
dc.subject.keywordPlus | CALCIUM-CHANNELS | - |
dc.subject.keywordPlus | TRANSMITTER RELEASE | - |
dc.subject.keywordPlus | DEVELOPMENTAL-CHANGES | - |
dc.subject.keywordPlus | ADENOSINE A(1) | - |
dc.subject.keywordPlus | CURRENTS | - |
dc.subject.keywordPlus | FACILITATION | - |
dc.subject.keywordPlus | INHIBITION | - |
dc.subject.keywordPlus | MODULATION | - |
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