Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection

Citation
Mc. Angulo et al., Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection, J NEUROSC, 19(5), 1999, pp. 1566-1576
Citations number
38
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROSCIENCE
ISSN journal
02706474 → ACNP
Volume
19
Issue
5
Year of publication
1999
Pages
1566 - 1576
Database
ISI
SICI code
0270-6474(19990301)19:5<1566:DSCITR>2.0.ZU;2-A
Abstract
Excitatory synaptic transmission between pyramidal cells and fast-spiking ( FS) interneurons of layer V of the motor cortex was investigated in acute s lices by using paired recordings at 30 degrees C combined with morphologica l analysis. The presynaptic and postsynaptic properties at these identified central synapses were compared between 3- and 5-week-old rats. At these tw o postnatal developmental stages, unitary EPSCs were mediated by the activa tion of AMPA receptors with fast kinetics at a holding potential of -72 mV. The amplitude distribution analysis of the EPSCs indicates that, at both s tages, pyramidal-FS connections consisted of multiple functional release si tes. The apparent quantal size obtained by decreasing the external calcium ([Ca2+](e)) varied from 11 to 29 pA near resting membrane potential, In you ng rats, pairs of presynaptic action potentials elicited unitary synaptic r esponses that displayed paired-pulse depression at all tested frequencies. In older animals, inputs from different pyramidal cells onto the same FS in terneuron had different paired-pulse response characteristics and, at most of these connections, a switch from depression to facilitation occurred whe n decreasing the rate of presynaptic stimulation. The balance between facil itation and depression endows pyramidal-FS connections from 5-week-old anim als with wide integrative capabilities and confers unique functional proper ties to each synapse.