Abstract
It was the aim of this study to elucidate (1) how long the inhibitory action of sulfonylureas on (pro-) insulin biosynthesis in vitro persists and (2) whether a compensatory increase of hormone synthesis occurs following exposure of isolated islets to sulfonylureas.
Collagenase-isolated pancreatic rat islets were preexposed for a long (2 hours, scheme A) or short period (30 min, scheme B) to tolbutamide or glibenclamide. The washed islets were then labelled with 3 H-leucine for 2 hours. In experiments of type B, an intermediate incubation was carried out for 90 min in the presence of glucose only prior to labelling. (Pro-) Insulin biosynthesis was estimated from incorporation data for 3 H-leucine.
Preexposure of islets for 2 hours, but not for 30 min, to tolbutamide at low glucose markedly reduced subsequent 3 H-leucine incorporation into proinsulin and insulin. Preexposure to glibenclamide did not influence subsequent 3 H-leucine incorporation (protocol A) whereas, when tested after longer time periods, hormone biosynthesis was found slightly reduced (protocol B). Long prestimulation with high - instead of low - glucose increased the following 3 H-leucine incorporation into (pro-) insulin. The stimulatory action on insulin release persisted for several hours following preexposure to glibenclamide. After a high glucose stimulus for 2 hours an elevated insulin secretion rate was observed too.
Conclusions: (1) Sulfonylureas reduce insulin biosynthesis in vitro also several hours after withdrawal of the drug. (2) No rebound of hormone biosynthesis is apparent after sulfonylureas. A feedback of the insulin storage pool on insulin biosynthesis could not be demonstrated.
Key words
Sulfonylureas - Tolbutamide - Glibendamide - Insulin Biosynthesis - Proinsulin Biosynthesis - Insulin Secretion - Insulin Storage Pool - Isolated Pancreatic Islets
1 This part of the studies was included in the thesis of D.S.
2 Supported by Deutsche Forschungsgemeinschaft, Bonn - Bad Godesberg
