Endothelin-1 (ET-1)-potentiated insulin secretion:: Involvement of protein kinase C and the ETA receptor subtype

Endothelin-l (ET-1), a potent vasoconstrictor peptide of endothelial origin, is capable of influencing hormone secretion from endocrine tissues, eg, pancreatic islet cells. We have shown a direct stimulatory effect of ET-1 on insulin secretion from isolated mouse islets of Langerhans. However, it is unknown as to whether the peptide acts through specific receptors on the islet cells and which mechanisms are involved in this insulinotropic action. We have therefore used the specific ETA receptor antagonist BQ123, the ETB receptor agonist BQ3020, and classic alpha- and beta-adrenergic and cholinergic antagonists. ET-1 (100 nmol/L) stimulated insulin secretion from islets incubated at 8.3, 11.1, 16.7, and 25 mmol/L glucose (P < .05), At 3.3 mmol/L glucose, no alteration in insulin secretion was found. The cholinergic receptor antagonist atropine (5 mu mol/L) or the adrenergic receptor antagonists propranolol (5 mu mol/L) or phentolamine (5 mu mol/L) did not affect ET-1 (100 nmol/l)-stimulated insulin secretion. BQ123 (10 pmol/L to 10 mu mol/L) and BQ3020 (1 nmol/L to 1 mu mol/L) had no effect on glucose (16.7 mmol/L)-stimulated insulin secretion, but BQ123 counteracted the stimulatory effect of ET-1 (100 nmol/L) at concentrations of 1 nmol/L to 10 mu mol/L (P < .01). We also studied the relative role of protein kinase C (PKC) and a Wortmannin-sensitive pathway for ET-l-induced insulin secretion using 12-O-tetradecanoyl phorbol-13-acetate (TPA), Calphostin C, and Wortmannin, respectively. At 5.6 mmol/L glucose, ET-l (100 nmol/L) had no effect per se, whereas in the presence of 1 mu mol/L TPA, which acutely stimulates PKC, the peptide did potentiate insulin secretion (P < .05). Furthermore, the insulinotropic effect of ET-1 at 16.7 mmol/L glucose was counteracted by the PKC inhibitor Calphostin C (P < .05) and by downregulation of PKC by 24 hours of exposure of islets to TPA (0.5 mu mol/L, P < .05). Wortmannin (1 mu mol/L) did not alter ET-1-potentiated insulin secretion. In conclusion, our results suggest that ET-1 acts through specific ET-1 receptors, most likely the ETA, subtype. Furthermore, PKC plays an essential role in the insulinotropic action of ET-1 in mouse islets. Copyright (C) 2000 by W.B. Saunders Company.