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GABA B receptors mediate frequency‐dependent depression of excitatory potentials in rat perirhinal cortex in vitro
Author(s) -
Ziakopoulos Zoe,
Brown Malcolm W.,
Bashir Zafar I.
Publication year - 2000
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.1460-9568.2000.00965.x
Subject(s) - neuroscience , excitatory postsynaptic potential , stimulation , long term depression , entorhinal cortex , chemistry , perirhinal cortex , gabaa receptor , neurotransmission , receptor , glutamate receptor , medicine , biology , inhibitory postsynaptic potential , hippocampus , epilepsy , temporal lobe , biochemistry , ampa receptor
Excitatory synaptic transmission in the perirhinal cortex exhibits marked homosynaptic paired pulse depression (PPD) at inter‐pulse intervals between 100 and 1000 ms, being maximal at 200 ms. Additionally, there is greater PPD with stimulation of the pathway from the temporal cortex side than with stimulation of the pathway from the entorhinal cortex side. We establish that this frequency‐dependent depression relies on the activation of GABA B (γ‐aminobutyric acid) receptors. PPD in both temporal and entorhinal pathways is abolished by either of the selective GABA B receptor antagonists, 3‐N[1‐( s )‐(3,4‐dichlorophenyl)ethyl]amino‐2‐( s )‐hydroxypropyl‐p‐benzyl‐phosphinic acid (CGP55845A) or 3‐amino‐propyl(diethoxymethyl)phosphinic acid (CGP35348). Barium which blocks G‐protein‐coupled, inwardly rectifying potassium channels, does not block PPD. Heterosynaptic depression mediated by GABA B receptors was also observed. The depression of the entorhinal pathway by stimulation of the temporal pathway is greater than depression of the temporal pathway by stimulation of the entorhinal pathway. Moreover, PPD increases with stimulus strength and the depression is enhanced by short trains of stimuli, consistent with stronger stimulation resulting in more GABA reaching GABA B receptors on excitatory glutamatergic synapses. Synaptic activation of GABA B receptors may be important in regulating excitability in a frequency‐dependent manner with maximal depression occurring at ∼ 5 Hz, which approximates to the theta rhythm. That homosynaptic and heterosynaptic depression by stimulation of the temporal pathway is greater than by stimulation of the entorhinal pathway suggests that activation of temporal feedforward connections to the perirhinal cortex can dominate the GABAergic control of synaptic activity within the perirhinal cortex.