Fatty acid inhibition of glucose-stimulated insulin secretion is enhanced in pancreatic islets from insulin-resistant rats

A study was initiated to test two hypotheses. The first was the postulate t hat glucose stimulated insulin secretion would be enhanced in pancreatic is lets isolated from normal non-obese rats made insulin-resistant by dietary means. The second, related hypothesis was that glucose-stimulated insulin s ecretion by pancreatic islets isolated from insulin-resistant rats would be more vulnerable to inhibition following culture in the presence of fatty a cids. For this purpose, insulin resistance was induced in normal Sprague-Da wley rats by feeding fat-enriched and fructose-enriched diets. The results indicate that islets isolated from either fat-fed or fructose-fed rats secr eted significantly more insulin at a glucose concentration of 2.5 to 10.0 m mol/L. In addition, the mean maximal glucose (27 mmol/L)-stimulated insulin secretion rate was significantly lower (15.3 +/- 2.5 ng/islet/h) in islets from fructose-fed rats versus chow-fed rats (25.2 +/- 3.1 ng/islet/h) foll owing culture for 48 hours in the presence of palmitate (0.125 mu mol/L). T hese results support the view that glucose-stimulated insulin secretion is enhanced in islets from insulin-resistant rats, and that these islets are m ore vulnerable to the inhibitory effects of free fatty acid (FFA) on insuli n secretion. Copyright (C) 1999 by W.B. Saunders Company.