Synchronization of rat hippocampal neurons in the absence of excitatory amino acid-mediated transmission

Abstract

Extracellular and intracellular recordings and measurements of extracellular K + concentration ([K +] o) were performed in the adult rat hippocampus in an in vitro slice preparation. Excitatory amino acid receptor antagonists, as well as the K +-channel blockers 4-aminopyridine (4AP, 50 μM) and/or tetraethylammonium (TEA, 5 mM), were added to the bath. Synchronous, negative-going field potentials were recorded in the CA3 stratum radiatum during application of 4AP and excitatory amino acid receptor antagonists. Each of these events was associated with an intracellular long-lasting depolarization and a concomitant rise in [K +] o that attained peak values of 4.3 + 0.1 mM (mean ± S.E.M., n = 6 slices) and lasted 29 ± 3 s. These field potentials were still recorded in CA3 stratum radiatum after addition of TEA. Under these conditions, prolonged field potentials (40.2 ± 4.5 s, n = 18) characterized by a prominent positive component; discharge of population spikes also occurred. [K +] o, increases associated with these prolonged field-potential discharges had a considerable variability in magnitude (peak value = 3.8–14.1 mM, 6.1 ± 0.7 mM, n = 5) and duration (14–210 s; 48 ± 13 s, n = 5). In 8% of the cases spreading depression-like episodes were observed. [K +] o increases during spreading depression-like episodes attained peak values of 11–27 mM (22.8 ± 0.2 mM, n = 2) and had a duration of 160–396 s (244 ± 29 s, n = 2). All types of synchronous activity were abolished by the GABAA receptor antagonist bicuculline methiodide (t0 μM) ( n= 11). A similar effect was obtained by applying Ca 2+-free/high-Mg 2+ medium ( n = 5). Simultaneous field-potential recordings in CA3, CAI, dentate area and subiculum demonstrated that negative-going potentials and prolonged field-potential discharges occurred in all areas in a synchronous fashion. Spreading depression-like episodes were more frequently recorded in the CAI than in the CA3 area and were not seen in the subiculum or dentate area. These experiments indicate that a glutamatergic-independent, synchronous GABA-mediated potential which is elicited by 4AP in the adult rat hippocampus continues to occur in the presence of TEA. In addition, concomitant application of these K +-channel blockers induces a novel type of prolonged field-potential discharge as well as spreading depression-like episodes. Since all synchronous potentials (including spreading depression-like episodes) were abolished by bicuculline methiodide, we conclude that their occurrence is presumably dependent upon the post-synaptic activation of GABA A receptors located on neuronal and glial elements. As excitatory synaptic transmission was nominally blocked under our experimental conditions, we also propose that rises in [K +] o and consequent redistribution processes are per se sufficient to make all types of synchronous activity propagate.