Cerebellar neurones show complex and differentiated mechanisms of action potential generationthat have been proposed to depend on peculiarproperties of their voltage-dependent Na+currents. In this study we analysed voltage-dependent Na+currents of rat cerebellar granulecells (GCs) by performing whole-cell, patch-clamp experiments in acute rat cerebellar slices.A transient Na+current (INaT) was always present and had the properties of a typicalfast-activating/inactivating Na+current. In addition toINaT, robust persistent (INaP) andresurgent (INaR)Na+currents were observed.INaPpeaked at∼−40 mV, showed half-maximalactivation at∼−55 mV, and its maximal amplitude was about 1.5% of that ofINaT.INaRwaselicited by repolarizing pulses applied following step depolarizations able to activate/inactivateINaT, and showed voltage- and time-dependent activation and voltage-dependent decay kinetics.The conductance underlyingINaRshowed a bell-shaped voltage dependence, with peak at−35 mV. A significant correlation was found between GCINaRandINaTpeak amplitudes; however,GCs expressingINaTof similar size showed marked variability in terms ofINaRamplitude, andin a fraction of cellsINaRwas undetectable.INaT,INaPandINaRcould be accounted for by a13-state kinetic scheme comprising closed, open,inactivated and blocked states. Current-clampexperiments carried out to identify possible functional correlates ofINaPand/orINaRrevealedthat in GCs single action potentials were followed by depolarizing afterpotentials (DAPs). In amajority of cells, DAPs showed properties consistent withINaRplaying a role in their generation.Computer modelling showed thatINaRpromotes DAP generation and enhances high-frequencyfiring, whereasINaPboosts near-threshold firing activity. Our findings suggest that specialproperties of voltage-dependent Na+currents provides GCs with mechanisms suitable forshaping activity patterns, with potentially important consequences for cerebellar informationtransfer and computation.

Kinetic and functional analysis of transient, persistent, and resurgent sodium currents in rat cerebellar granule cells in situ: an electrophysiological and modelling study

FORTI, LIA CHIARA;
2006-01-01

Abstract

Cerebellar neurones show complex and differentiated mechanisms of action potential generationthat have been proposed to depend on peculiarproperties of their voltage-dependent Na+currents. In this study we analysed voltage-dependent Na+currents of rat cerebellar granulecells (GCs) by performing whole-cell, patch-clamp experiments in acute rat cerebellar slices.A transient Na+current (INaT) was always present and had the properties of a typicalfast-activating/inactivating Na+current. In addition toINaT, robust persistent (INaP) andresurgent (INaR)Na+currents were observed.INaPpeaked at∼−40 mV, showed half-maximalactivation at∼−55 mV, and its maximal amplitude was about 1.5% of that ofINaT.INaRwaselicited by repolarizing pulses applied following step depolarizations able to activate/inactivateINaT, and showed voltage- and time-dependent activation and voltage-dependent decay kinetics.The conductance underlyingINaRshowed a bell-shaped voltage dependence, with peak at−35 mV. A significant correlation was found between GCINaRandINaTpeak amplitudes; however,GCs expressingINaTof similar size showed marked variability in terms ofINaRamplitude, andin a fraction of cellsINaRwas undetectable.INaT,INaPandINaRcould be accounted for by a13-state kinetic scheme comprising closed, open,inactivated and blocked states. Current-clampexperiments carried out to identify possible functional correlates ofINaPand/orINaRrevealedthat in GCs single action potentials were followed by depolarizing afterpotentials (DAPs). In amajority of cells, DAPs showed properties consistent withINaRplaying a role in their generation.Computer modelling showed thatINaRpromotes DAP generation and enhances high-frequencyfiring, whereasINaPboosts near-threshold firing activity. Our findings suggest that specialproperties of voltage-dependent Na+currents provides GCs with mechanisms suitable forshaping activity patterns, with potentially important consequences for cerebellar informationtransfer and computation.
2006
2006
J., Magistretti; L., Castelli; Forti, LIA CHIARA; E., Dangelo
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/1681130
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