Presynaptic N-type and P/Q-type Ca2+ channels mediating synaptic transmission at the calyx of held of mice
- Authors
- Ishikawa, T; Kaneko, M; Shin, HS; Takahashi, 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
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