Arachidonic acid is a physiological activator of the ryanodine receptor in pancreatic β-cells

Pancreatic beta-cells have ryanodine receptors but little is known about their physiological regulation. Previous studies have shown that arachidonic acid releases Ca2+ from intracellular stores in beta-cells but the identity of the channels involved in the Ca2+ release has not been elucidated. We studied the mechanism by which arachidonic acid induces Ca2+ concentration changes in pancreatic beta-cells. Cytosolic free Ca2+ concentration was measured in fura-2-loaded INS-1E cells and in primary beta-cells from Wistar rats. The increase of cytosolic Ca2+ concentration induced by arachidonic acid (150 mu M) was due to both Ca2+ release from intracellular stores and influx of Ca2+ from extracellular medium. 5,8,11,14-Eicosatetraynoic acid, a non-metabolizable analogue of arachidonic acid, mimicked the effect of arachidonic acid, indicating that arachidonic acid itself mediated Ca2+, increase. The Ca2+ release induced by arachidonic acid was from the endoplasmic reticulum since it was blocked by thapsigargain. 2-Aminoethyl diphenylborinate (50 VLM), which is known to inhibit 1,4,5-inositol-triphosphate-receptors, did not block Ca2+ release by arachidonic acid. However, ryanodine (100 VM), a blocker of ryanodine receptors, abolished the effect of arachidonic acid on Ca2+ release in both types of cells. These observations indicate that arachidonic acid is a physiological activator of ryanodine receptors in beta-cells. (c) 2006 Elsevier Ltd. All rights reserved.