EVIDENCE FOR PHOSPHORAMIDON-SENSITIVE CLEAVAGE OF BIG ENDOTHELIN-1 INVOLVED IN ENDOTHELIN-STIMULATED HEPATIC GLUCOSE-PRODUCTION

Endothelin-l (ET-1) is known to stimulate glycogenolysis in perfused r at livers and isolated rat hepatocytes. To determine the potential act ion of endothelin's precursor, big endothelin-l (big ET-1), isolated r at livers were perfused with big ET-1 in a non-recirculating system. T hereby, big ET-1 (10 nM) induced a maximally threefold increase (P<0.0 1 vs. basal values) in hepatic glucose production at 60 min, which was almost completely abolished by concomitant infusion of 50 mu M phosph oramidon, a sensitive inhibitor of the enzymatic cleavage of big ET-1 to ET-1. The corresponding incremental release of glucose by big ET-1 was 20.9-fold higher in the absence of phosphoramidon than in its pres ence (P<0.01). In contrast, phosphoramidon did not inhibit hepatic glu cose production induced by ET-I (1 nM), glucagon (1 nM), and phenyleph rine (5 mu M). Glycogenolytic responses to 1 nM ET-I (P<0.01), but not to 1 nM glucagon (n.s.) were blocked by indomethacin (100 mu M), indi cating that prostaglandin release by non-parenchymal cells is at least in part involved in the hepatic ET-1 action. In conclusion, big ET-1 induces hepatic glucose release, which is suggested to depend on intra hepatic conversion of big ET-1 to ET-1 by a phosphoramidon-sensitive p athway.