Extracellular field potentials (fEPSPs) and whole cell patch-clamp recordings were used to test the effect of S 38232, a newly developed potent non-?7 nicotinic acetylcholine receptors (nAChR) agonist, on synaptic transmission in hippocampal slices obtained from adult mice.S 38232 increased the amplitude of fEPSPs, evoked in stratum radiatum by Schaffer collateral stimulation. This effect was potentiated by picrotoxin, suggesting that S 38232 exerts at least in part its effect on GABAergic interneurons. The action of S 38232 was mediated by non-?7 containing nAChRs since it was prevented by DH?E (1 ?M) but not by ?-BTX (100. nM). A similar potentiating effect on fEPSPs was observed when nicotine (1 ?M) was applied to hippocampal slices obtained from ?7 -/- mice in the presence of picrotoxin. The potentiating effect of S 38232 was probably presynaptic in origin since it was associated with a significant reduction in paired-pulse ratio.In addition, in patch clamp experiments, S 38232 enhanced the frequency (but not the amplitude) of spontaneous excitatory and inhibitory postsynaptic currents (sEPSCs, sIPSCs) recorded from CA1 principal cells. Moreover, it enhanced the frequency of miniature IPSCs but not EPSCs, suggesting that it was acting on nAChRs located on presynaptic/pre-terminal regions of GABAergic interneurons. The effect of S 38232 on GABAergic signaling was concentration-dependent with an EC of 43?M.In conclusions, we present evidence that the new nicotine ligand S 38232, by selectively activating non-?7 nAChRs located on principal cells and GABAergic interneurons, influences network activity and information processing in the hippocampus. © 2009 Elsevier Ltd.
Modulatory effects of S 38232, a non ?-7 containing nicotine acetylcholine receptor agonist on network activity in the mouse hippocampus
Lagostena Laura;
2010
Abstract
Extracellular field potentials (fEPSPs) and whole cell patch-clamp recordings were used to test the effect of S 38232, a newly developed potent non-?7 nicotinic acetylcholine receptors (nAChR) agonist, on synaptic transmission in hippocampal slices obtained from adult mice.S 38232 increased the amplitude of fEPSPs, evoked in stratum radiatum by Schaffer collateral stimulation. This effect was potentiated by picrotoxin, suggesting that S 38232 exerts at least in part its effect on GABAergic interneurons. The action of S 38232 was mediated by non-?7 containing nAChRs since it was prevented by DH?E (1 ?M) but not by ?-BTX (100. nM). A similar potentiating effect on fEPSPs was observed when nicotine (1 ?M) was applied to hippocampal slices obtained from ?7 -/- mice in the presence of picrotoxin. The potentiating effect of S 38232 was probably presynaptic in origin since it was associated with a significant reduction in paired-pulse ratio.In addition, in patch clamp experiments, S 38232 enhanced the frequency (but not the amplitude) of spontaneous excitatory and inhibitory postsynaptic currents (sEPSCs, sIPSCs) recorded from CA1 principal cells. Moreover, it enhanced the frequency of miniature IPSCs but not EPSCs, suggesting that it was acting on nAChRs located on presynaptic/pre-terminal regions of GABAergic interneurons. The effect of S 38232 on GABAergic signaling was concentration-dependent with an EC of 43?M.In conclusions, we present evidence that the new nicotine ligand S 38232, by selectively activating non-?7 nAChRs located on principal cells and GABAergic interneurons, influences network activity and information processing in the hippocampus. © 2009 Elsevier Ltd.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
