Block of Na+ currents and suppression of action potentials in embryonic rat dorsal root ganglion neurons by ranolazine

Ranolazine, an anti-anginal drug, reduces neuropathic and inflammatory-induced allodynia in rats. However, the mechanism of ranolazin’s anti-allodynic effect is not known. We hypothesized that ranolazine would reduce dorsal root ganglion (DRG) Na(+) current (I(Na)) and neuronal firing by stabilizing Na(+) channels in inactivated states to cause voltage- and frequency-dependent block. Therefore, we investigated the effects of ranolazine on tetrodotoxin-sensitive (TTXs) and tetrodotoxin-resistant (TTXr) I(Na) and action potential parameters of small diameter DRG neurons from embryonic rats. Ranolazine (10 and 30 muM) significantly reduced the firing frequency of evoked action potentials in DRG neurons from 19.2 +/- 1.4 to 9.8 +/- 2.7 (10 muM) and 5.7 +/- 1.3 (30 muM) Hz at a resting membrane potential of -40 mV. Ranolazine blocked TTXs and TTXr in a voltage- and frequency-dependent manner. Furthermore, ranolazine (10 muM) blocked hNa(v)1.3 (expressed in HEK293 cells) and caused a hyperpolarizing shift in the voltage dependence of steady-state intermediate and slow inactivation Na(v)1.3 current. Taken together, the results suggest that ranolazine suppresses the hyperexcitability of DRG neurons by interacting with the inactivated states of Na(+) channels and these actions may contribute to its anti-allodynic effect in animal models of neuropathic pain

Keywords : Acetanilides,Action Potentials,Animals,Cells,Cultured,drug effects,embryology,Ganglia,Spinal,Hek293 Cells,Humans,NAV1.3 Voltage-Gated Sodium Channel,Neurons,Pain,pharmacology,physiology,Piperazines,Ranolazine,Rats,Sodium,Sodium Channel Blockers,Sodium Channels,, Na(+),Currents,Suppression, west london physio

Date of Publication : 2012 Jun

Authors : Hirakawa R;El-Bizri N;Shryock JC;Belardinelli L;Rajamani S;

Organisation : Department of Biology, Gilead Sciences Inc., 1651 Page Mill Road, Palo Alto, CA 94304, USA

Journal of Publication : Neuropharmacology

Pubmed Link : https://www.ncbi.nlm.nih.gov/pubmed/22313527

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