Up-regulation of low-threshold tetrodotoxin-resistant Na+ current via activation of a cyclic AMP/protein kinase A pathway in nociceptor-like rat dorsal root ganglion cells

The effects of forskolin on low-threshold tetrodotoxin-resistant (TTX-r) Na+ currents was studied in small diameter (average ≈ 25 μm) dorsal root ganglion (DRG) cells. All DRG cells included in the study were categorized as type-2 or non-type-2 based on the expression of a low-threshold A-current. In all type-2 and some non-type-2 DRG cells held at −80 mV, the adenylyl cyclase (AC) activator forskolin (10 μM) up-regulated TTX-r Na+ currents evoked with steps to −55 mV through −35 mV (low-threshold current). Up-regulation of low-threshold current by forskolin was mimicked by the protein kinase A (PKA) agonist Sp-cAMPs and the inflammatory mediator serotonin, and blocked by the PKA antagonist Rp-cAMPs. Forskolin-induced up-regulation of low-threshold current evoked from a holding potential of −60 mV was blocked by 40 ms steps to 0 mV, which presumably induced a long lasting inactivation of the low-threshold channels. Reducing to 3 ms the duration of steps to 0 mV, significantly increased the number of DRG cells where low-threshold current was up-regulated by forskolin, presumably by reducing the long-lasting inactivation of the low-threshold channels. In the same cells, high-threshold current, evoked by 40 ms or 3 ms steps to 0 mV, was consistently up-regulated by forskolin. The selective NaV1.8 channel blocker A-803467 markedly blocked high-threshold current but not low-threshold current. The different voltage protocols observed to activate and inactivate the low- and high-threshold currents, and the observation that A-803467 blocked high- but not low-threshold current suggests that the two currents were mediated by different channels, possibly NaV1.8 and NaV1.9, respectively. Inflammatory mediators may simultaneously up-regulate NaV1.8 and NaV1.9 channels in the same nociceptor via a AC/PKA signaling pathway, increasing nociceptor signaling strength, and lowering nociceptor threshold, respectively.

▶Forskolin up-regulated low-threshold Na+ currents in nociceptor-like DRG cells. ▶Experiments with a PKA agonist and antagonist show forskolin acted via PKA. ▶Forskolin increased the amplitude of current evoked by steps to −55 mV. ▶The low-threshold current was not blocked by the NaV1.8 blocker A-803467. ▶Properties of the low-threshold current suggest it was mediated by NaV1.9 channels.