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Presynaptic short‐term depression is maintained during regulation of transmitter release at a GABAergic synapse in rat hippocampus
Author(s) -
Hefft Stefan,
Kraushaar Udo,
R. P. Geiger Jörg,
Jonas Peter
Publication year - 2002
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2001.013455
Subject(s) - inhibitory postsynaptic potential , neurotransmission , neuroscience , postsynaptic potential , dentate gyrus , chemistry , hippocampus , postsynaptic current , biophysics , biology , excitatory postsynaptic potential , receptor , biochemistry
To examine possible interactions between fast depression and modulation of inhibitory synaptic transmission in the hippocampus, we recorded from pairs of synaptically connected basket cells (BCs) and granule cells (GCs) in the dentate gyrus of rat brain slices at 34 °C. Multiple‐pulse depression (MPD) was examined in trains of 5 or 10 inhibitory postsynaptic currents (IPSCs) evoked at frequencies of 10–00 Hz under several conditions that inhibit transmitter release: block of voltage‐dependent Ca 2+ channels by Cd 2+ (10 μ m ), activation of γ‐amino‐butyric acid type B receptors (GABA B Rs) by baclofen (10 μ m ) and activation of muscarinic acetylcholine receptors (mAchRs) by carbachol (2 μ m ). All manipulations led to a substantial inhibition of synaptic transmission, reducing the amplitude of the first IPSC in the train (IPSC 1 ) by 72 %, 61 % and 29 %, respectively. However, MPD was largely preserved under these conditions (0.34 in control versus 0.31, 0.50 and 0.47 in the respective conditions at 50 Hz). Similarly, a theta burst stimulation (TBS) protocol reduced IPSC 1 by 54 %, but left MPD unchanged (0.40 in control and 0.39 during TBS). Analysis of both fractions of transmission failures and coefficients of variation (CV) of IPSC peak amplitudes suggested that MPD had a presynaptic expression site, independent of release probability. In conclusion, different types of presynaptic modulation of inhibitory synaptic transmission converge on a reduction of synaptic strength, while short‐term dynamics are largely unchanged.