Reactive blue 2, an antagonist of rat P2Y 4, increases K + secretion in rat cochlea strial marginal cells

Abstract

Extracellular ATP decreases K + secretion in strial marginal cells via apical P2Y 4 receptors. We investigated the effect of reactive blue 2 (RB-2), an antagonist of rat P2Y 4, on rat strial marginal cells using a voltage-sensitive vibrating probe. The application of RB-2 increased K + secretion in a dose-dependent manner, and this increase was characterized as a peak followed by a partial relaxation to a steady-state. Moreover, this response was similar to that caused by 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid (DIDS). Suramin had no similar effect, except at high concentration. Thus, we tested the effects of these chemicals on P2Y 4 receptors in strial marginal cells. Both RB-2 and DIDS had antagonistic activities at P2Y 4, and the antagonist potency at P2Y 4 paralleled the potency of K + secretion. Interestingly, 2′- and 3′-O-(4-benzoyl-benzoyl)adenosine 5′-triphosphate (BzATP) exhibited an agonistic effect at P2Y 4 receptor, which was blocked by RB-2, but not by pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid (PPADS). Based on these results, we speculate that direct and/or indirect inhibitory mechanisms between P2Y 4 and KENQ1/KCNE1 K + channels exist in strial marginal cell.