Abstract
In order to assess further the mechanisms involved in insulin release, we prelabeled rat pancreatic islets of Langerhans by incubating either 45Ca or [2-3H]adenine. When prelabeled islets were perfused with a glucose-free medium (the experiment with 45Ca) and a medium containing 2.8mM glucose (the experiment with [2-3H] adenine) respectively, a constant rate of efflux of the radioactivity was established by 30min in each case. D-Glucose at 16.7mM concentration elicited a rapid efflux of 45Ca and [2-3H] adenine derivatives ([3H]Ad) within 4 to 6 min after commencing the step-wise stimulation by glucose, concomitantly with insulin release. However, Lglucose and D-galactose little stimulated both 45Ca and [3H] Ad release. Lanthanum chloride caused a burst peak of 45Ca release in the absence of glucose. A rapid efflux of45Ca was caused by fi-D-glucose and D-glyceraldehyde to much lesser extent than by α-D-glucose.
The slowly rising concentration of glucose at 0.1mm/min of gradient level failed to elicit any rapid efflux of 45Ca or [3H] Ad, although insulin release occurred in accordance with an increase in glucose concentration. Even when the gradient of glucose concentration was raised to 0.7mM/min, glucose failed to stimulate an efflux of [3H] Ad but the subsequent stimulation by 16.7mM glucose caused a rapid efflux of [3H] Ad concomitantly with the release of insulin. No rapid efflux of 45Ca was observed under a slow-rise glucose stimulation until the gradient level of the glucose concentration was raised to 6.7mM.
Analysis of distribution of the radioactive adenine derivatives after incubation showed that the adenosine fraction had the highest radioactivity in the medium followed by the ATP, adenine and cAMP fraction in that order, and the ATP fraction had the highest radioactivity in the islet. The ratio of radioactivity in the cAMP fraction in the medium to the total count was the highest among all.
On the basis of these results, it was suggested that the discharge of [3H] Ad and 45Ca might occur with the alteration of the membrane permeability induced by a rapid change of the glucose concentration, and that their discharge might perhaps link to the glucoreceptor mechanism directly controlling insulin release.
