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J Neurophysiol 90: 712-722, 2003. First published April 23, 2003; doi:10.1152/jn.01109.2002
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Voltage- and Activity-Dependent Chloride Conductance Controls the Resting Status of the Intact Rat Sympathetic Neuron

Oscar Sacchi1, Maria Lisa Rossi1, Rita Canella1 and Riccardo Fesce2

1 Department of Biology, Section of Physiology and Biophysics and Centre of Neuroscience, Ferrara University, 44100 Ferrara, Italy; 2 Centre of Neuroscience, Insubria University, 21100 Varese, Italy

Submitted 11 December 2002; accepted in final form 15 April 2003

Remarkable activity dependence was uncovered in the chloride conductance that operates in the subthreshold region of membrane potential, by using the two-microelectrode voltage-clamp technique in the mature and intact rat sympathetic neuron. Both direct and synaptic neuron tetanization (15 Hz, 10-s duration to saturate the response) resulted in a long-lasting (not less than 15 min) increase of cell input conductance (+70–150% 10 min after tetanus), accompanied by the onset of an inward current with the same time course. Both processes developed with similar properties in the postganglionic neuron when presynaptic stimulation was performed under current- or voltage-clamp conditions and were unaffected by external calcium on direct stimulation. The posttetanic effects were sustained by gCl increase because both conductance and current modifications were blocked by 0.5 mM Anthracene-9-carboxylic acid (a chloride channel blocker) but were unaffected by TEACl or cesium chloride treatments. The chloride channel properties were modified by stimulation: their voltage sensitivity and rate of closure in response to hyperpolarization strongly increased. The voltage dependence of the three major conductances governing the cell subthreshold status (gCl, gK, and gL) was evaluated over the –40/–110 mV membrane potential range in unstimulated neurons and compared with previous results in stimulated neurons. A drastic difference between the voltage-conductance profiles was observed, exclusively sustained by gCl increase. The chloride channel thus hosts an intrinsic mechanism, a memory of previous neuron activity, which makes the chloride current a likely candidate for natural controller of the balance between opposite resting currents and thus of membrane potential level.


Address for reprint requests: O. Sacchi, Dept. of Biology, Section of Physiology and Biophysics, Via Borsari 46, I-44100 Ferrara, Italy (E-mail: sho{at}dns.unife.it).







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