Inhibition by Pregnenolone Sulphate, a Metabolite of the Neurosteroid Pregnenolone, of Voltage-Gated Sodium Channels Expressed in Xenopus Oocytes

Abstract

Neurosteroids are known as allosteric modulators of the ligand-gated ion channel superfamily. Voltage-gated sodium channels (Na_v) play an important role in mediating excitotoxic damages. Here we report the effects of neurosteroids on the function of Na_v, using voltage-clamp techniques in Xenopus oocytes expressed with the Na_v1.2 α subunit. Pregnenolone sulphate, but not pregnenolone, inhibited sodium currents (I_Na) at 3 – 100 μmol/L. The suppression of I_Na by pregnenolone sulphate was due to increased inactivation with little change in activation. These findings suggest that pregnenolone sulphate, a metabolite of pregnenolone, suppresses the function of Na_v via increased inactivation, which may contribute to the neuroprotection.