Multiple types of high-voltage-activated Ca2+ channels trigger neurotransmi
tter release at the mammalian central synapse. Among them, the omega-conoto
xin GVIA-sensitive N-type channels and the omega-Aga-IVA-sensitive P/Q-type
channels mediate fast synaptic transmission. However, at most central syna
pses, it is not known whether the contributions of different Ca2+ channel t
ypes to synaptic transmission remain stable throughout postnatal developmen
t. We have addressed this question by testing type-specific Ca2+ channel bl
ockers at developing central synapses. Our results indicate that N-type cha
nnels contribute to thalamic and cerebellar IPSCs only transiently during e
arly postnatal period and P/Q-type channels predominantly mediate mature sy
naptic transmission, as we reported previously at the brainstem auditory sy
napse formed by the calyx of Held. In fact, Ca2+ currents directly recorded
from the auditory calyceal presynaptic terminal were identified as N-, P/Q
-, and R-types at postnatal day 7 (P7) to P10 but became predominantly P/Q-
type at P13. In contrast to thalamic and cerebellar IPSCs and brainstem aud
itory EPSCs, N- type Ca2+ channels persistently contribute to cerebral cort
ical EPSCs and spinal IPSCs throughout postnatal months. Thus, in adult ani
mals, synaptic transmission is predominantly mediated by P/Q-type channels
at a subset of synapses and mediated synergistically by multiple types of C
a2+ channels at other synapses.