Presynaptic N-type and P/Q-type Ca2+ channels mediating synaptic transmission at the calyx of held of mice

Authors
Ishikawa, TKaneko, MShin, HSTakahashi, T
Issue Date
2005-10-01
Publisher
WILEY
Citation
JOURNAL OF PHYSIOLOGY-LONDON, v.568, no.1, pp.199 - 209
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.
Keywords
SHORT-TERM DEPRESSION; GTP-BINDING PROTEIN; CALCIUM-CHANNELS; TRANSMITTER RELEASE; DEVELOPMENTAL-CHANGES; ADENOSINE A(1); CURRENTS; FACILITATION; INHIBITION; MODULATION; SHORT-TERM DEPRESSION; GTP-BINDING PROTEIN; CALCIUM-CHANNELS; TRANSMITTER RELEASE; DEVELOPMENTAL-CHANGES; ADENOSINE A(1); CURRENTS; FACILITATION; INHIBITION; MODULATION
ISSN
0022-3751
URI
https://pubs.kist.re.kr/handle/201004/136061
DOI
10.1113/jphysiol.2005.089912
Appears in Collections:
KIST Article > 2005
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE