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J Neurophysiol 99: 2006-2011, 2008. First published February 6, 2008; doi:10.1152/jn.00911.2007
0022-3077/08 $8.00
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Ionic Basis of ON and OFF Persistent Activity in Layer III Lateral Entorhinal Cortical Principal Neurons

Babak Tahvildari1, Angel A. Alonso1,{maltese cross} and Charles W. Bourque2

1Department of Neurology and Neurosurgery, Montreal Neurological Institute and McGill University, Montreal; and 2Center for Research in Neuroscience, Montreal General Hospital and McGill University, Montreal, Canada

Submitted 15 August 2007; accepted in final form 3 February 2008

Principal neurons in layer III of the rat lateral entorhinal cortex (LEC) generate a self-sustained plateau potential and persistent spiking following the application of a brief suprathreshold excitatory stimulus delivered in the presence of the muscarinic receptor agonist carbachol. This persistent activity can be terminated by application of a second excitatory stimulus, and these cells can be repeatedly toggled between ON and OFF states by consecutive excitatory stimuli. However, the ionic mechanisms that underlie the production of ON and OFF states in layer III LEC neurons are unknown but seem to involve activity-dependent conductances, since they can be initiated by trains of action potentials evoked by either depolarizing current pulses applied to the cell or by repetitive spiking induced by activation of excitatory synaptic inputs. In this study, we obtained intracellular recordings from rat layer III LEC neurons in vitro, and a series of pharmacological and ionic substitution experiments were performed to identify mechanisms involved in the induction and termination of persistent spiking. Our data indicate that initiation of the ON state depends on spike-evoked calcium influx and subsequent activation of calcium-activated nonselective cationic current. Moreover, we show that termination of persistent firing in response to an excitatory stimulus can be blocked by tetraethylammonium or iberiotoxin, suggesting that the activation of calcium-activated potassium current mediated by large conductance calcium-activated K+ (i.e., BK) channels is required to induce the OFF state.


Address for reprint requests and other correspondence: C. W. Bourque, Div. of Neurology, Montreal General Hospital, 1650 Cedar Ave., Rm. L7-216, Montreal, QC H3G 1A4, Canada (E-mail: charles.bourque{at}mcgill.ca)




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