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Action potential broadening induced by lithium may cause a presynaptic enhancement of excitatory synaptic transmission in neonatal rat hippocampus
Author(s) -
Colino Asunción,
GarcíaSeoane Jorge J.,
Valentín Antonio
Publication year - 1998
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.1460-9568.1998.00255.x
Subject(s) - excitatory postsynaptic potential , neurotransmission , neural facilitation , neuroscience , postsynaptic potential , chemistry , inhibitory postsynaptic potential , postsynaptic current , ampa receptor , hippocampus , synaptic potential , lithium (medication) , biophysics , nmda receptor , biology , endocrinology , receptor , biochemistry
Lithium enhances excitatory synaptic transmission in CA1 pyramidal cells, but the mechanisms remain unclear. The present study demonstrates that lithium enhances the N ‐methyl‐ d ‐aspartate (NMDA) and α‐amino‐3‐hydroxy‐5‐methyl‐isoxazole propionic acid (AMPA) receptor‐mediated components of the excitatory postsynaptic current (EPSC). Lithium decreased the magnitude of paired‐pulse facilitation and presented an inverse correlation between the lithium‐induced enhancement of synaptic transmission and initial paired‐pulse facilitation, which is consistent with a presynaptic mode of action. The enhancement of synaptic strength is likely to act, at least in part, by increasing the amplitude of the presynaptic Ca 2+ transient. One mechanism which could account for this change of the presynaptic Ca 2+ transient is an increase in the duration of the action potential. We investigated action potential in hippocampal pyramidal neurons and found that lithium (0.5–6 m m ) increased the half‐amplitude duration and reduced the rate of repolarization, whereas the rate of depolarization remained similar. To find out whether the lithium synaptic effects might be explained by spike broadening, we investigated the field recording of the excitatory postsynaptic potential (EPSP) in hippocampal slices and found three lines of evidence. First, the prolongation of the presynaptic action potential with 4‐aminopyridine and tetraethylammonium blocked or reduced the synaptic effects of lithium. Second, the lithium‐induced synaptic enhancement was modulated when presynaptic Ca 2+ influx was varied by changing the external Ca 2+ concentration. Finally, both effects, the synaptic transmission increment and the action potential broadening, were independent of inositol depletion. These results suggest that lithium enhances synaptic transmission in the hippocampus via a presynaptic site of action: the mechanism underlying the potentiating effect may be attributable to an increased Ca 2+ influx consequent to the broadening effect of lithium on the action potential.