PT  - JOURNAL ARTICLE
AU  - Maki Koike-Tani
AU  - Naoto Saitoh
AU  - Tomoyuki Takahashi
TI  - Mechanisms Underlying Developmental Speeding in AMPA-EPSC Decay Time at the Calyx of Held
AID  - 10.1523/JNEUROSCI.3861-04.2005
DP  - 2005 Jan 05
TA  - The Journal of Neuroscience
PG  - 199--207
VI  - 25
IP  - 1
4099  - http://www.jneurosci.org/content/25/1/199.short
4100  - http://www.jneurosci.org/content/25/1/199.full
SO  - J. Neurosci.2005 Jan 05; 25
AB  - The time course of synaptic conductance is important in temporal precision of information processing in the neuronal network. The AMPA receptor (AMPAR)-mediated EPSCs at the calyx of Held become faster in decay time as animals mature. To clarify how desensitization and deactivation of AMPARs contribute to developmental speeding of EPSCs, we compared the decay time of quantal EPSCs (qEPSCs) with the deactivation and desensitization times of AMPAR currents induced in excised patches by fast glutamate application (AMPA patch currents). Both the deactivation and desensitization times of AMPA patch currents became markedly faster from postnatal day 7 (P7) to P14 and changed little thereafter. In individual neurons, throughout development (P7-P21), the time constants of deactivation and fast desensitization in AMPA patch currents were similar to each other and close to the qEPSC decay time constant. Cyclothiazide (CTZ) abolished the fast desensitization, prolonged deactivation of AMPA patch currents, and slowed the decay time of EPSCs. The effects of CTZ on AMPA patch currents were unchanged throughout development, whereas its effect on EPSCs became weaker as animals matured. In single-cell reverse transcription-PCR analysis, glutamate receptor subunit 4 (GluR4) flop increased from P7 to P14 and changed little thereafter. At P7, the GluR4 flop abundance had an inverse correlation with the qEPSC decay time. These results together suggest that both desensitization and deactivation of AMPARs are involved in the EPSC decay time, but the contribution of desensitization decreases during postnatal development at the calyx of Held.