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J Physiol Volume 586, Number 3, 803-815, February 1, 2008 DOI: 10.1113/jphysiol.2007.146019
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NEUROSCIENCE

Functional role of cyclic nucleotide-gated channels in rat medial vestibular nucleus neurons

Maria Vittoria Podda1, Marcello D'Ascenzo1, Lucia Leone1, Roberto Piacentini1, Gian Battista Azzena1 and Claudio Grassi1

1 Institute of Human Physiology, Medical School, Catholic University ‘S. Cuore’, I-00168 Rome, Italy

Although cyclic nucleotide-gated (CNG) channels are expressed in numerous brain areas, little information is available on their functions in CNS neurons. The aim of the present study was to define the distribution of CNG channels in the rat medial vestibular nucleus (MVN) and their possible involvement in regulating MVN neuron (MVNn) excitability. The majority of MVNn expressed both CNG1 and CNG2 A subunits. In whole-cell current-clamp experiments carried out on brainstem slices containing the MVNn, the membrane-permeant analogues of cyclic nucleotides, 8-Br-cGMP and 8-Br-cAMP (1 mM), induced membrane depolarizations (8.9 ± 0.8 and 9.2 ± 1.0 mV, respectively) that were protein kinase independent. The cGMP-induced depolarization was associated with a significant decrease in the membrane input resistance. The effects of cGMP on membrane potential were almost completely abolished by the CNG channel blockers, Cd2+ and L-cis-diltiazem, but they were unaffected by blockade of hyperpolarization-activated cyclic nucleotide-gated channels. In voltage-clamp experiments, 8-Br-cGMP induced non-inactivating inward currents (–22.2 ± 3.9 pA) with an estimated reversal potential near 0 mV, which were markedly inhibited by reduction of extracellular Na+ and Ca2+ concentrations. Membrane depolarization induced by CNG channel activation increased the firing rate of MVNn without changing the action potential shape. Collectively, these findings provide novel evidence that CNG channels affect membrane potential and excitability of MVNn. Such action should have a significant impact on the function of these neurons in sensory–motor integration processes. More generally, it might represent a broad mechanism for regulating the excitability of different CNS neurons.

(Received 7 October 2007; accepted after revision 28 November 2007; first published online 29 November 2007)
Corresponding author C. Grassi: Institute of Human Physiology, Medical School, Catholic University ‘S. Cuore’, Largo F. Vito 1, 00168 Rome, Italy. Email: grassi{at}rm.unicatt.it




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A. H. Gittis and S. du Lac
Similar Properties of Transient, Persistent, and Resurgent Na Currents in GABAergic and Non-GABAergic Vestibular Nucleus Neurons
J Neurophysiol, May 1, 2008; 99(5): 2060 - 2065.
[Abstract] [Full Text] [PDF]




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