Abstract

Insulin secretion in the intact organism, and by the perfused pancreas and groups of isolated perifused islets, is pulsatile. We have proposed a metabolic model of glucose-induced insulin secretion in which oscillations in the ATP/ADP ratio drive alterations in metabolic and electrical events that lead to insulin release. A key prediction of our model is that metabolically driven Ca2+ oscillations will also occur. Using the fluorescent Ca2+ probe, fura 2, digital image analysis, and sensitive O2 electrodes, we investigated cytosolic free Ca2+ responses and O2 consumption in perifused rat islets that had been maintained in culture for 1-4 days. We found that elevated ambient glucose increased the average cytosolic free Ca2+ level, the ATP/ADP ratio, and oxygen consumption, as previously found in freshly isolated islets. Oscillatory patterns were obtained for Ca2+, O2 consumption, and insulin secretion in the presence of 10 and 20 mM glucose. Very low amplitude oscillations in cytosolic free Ca2+ were observed at 3 mM nonstimulatory glucose levels. Evaluation of the Ca2+ responses of a large series of individual islets, monitored by digital image analysis and perifused at both 3 and 10 mM glucose, indicated that the rise in glucose concentration caused more than a doubling of the average cytosolic free Ca2+ value and a 4-fold increase in the amplitude of the oscillations with little change in period. The pattern of Ca2+ change within the islets was consistent with recruitment of responding cells. The coexistence of oscillations with similar periods in insulin secretion, oxygen consumption, and cytosolic free Ca2+ is consistent with the model of metabolically driven pulsatile insulin secretion.

Highlights

  • Insulin secretion in the intact organism, and by the in other cell types, because it is initiated by a change in fuel perfusedpancreas and groups of isolatedperifused metabolism rather than by the binding of an agonist to a islets, is pulsatile

  • It has of glucose-induced insulin secretion in which oscilla- muchin common withstimulatedsecretioninother cells, tions in theATP/ADP ratio drive alterations imneta- since it involves increases in cytosolic free Ca2+ and CAMP bolic and electrical events that lead to insulin release. ( 1, 3 ) and possibly production of diacylglycerol or other lipids disCoAserralenkie2vsset+ceisytenripnevtrCstheepaadOCo2tin+2castho2eiesa+olsbecdneciapletlnrnraoodotmdibfofeOeaunos,2i,srunacrwtwao2emini,nlsdloieunidadgmvelieslptsioatnitilsioogncticamhcuteaiulandttrgu. mpecrUeyeertastoiinaff1nsobua-ogrotsl4lyheliicsdedciafasfrryll,eulasye-.tandpti(so1elrAre,yf4tus,psst5a(er9td)it,k.ei1prnn0ag)nth.ccaThretahhariasasscpb(te8uer)leis,snaatitncildiotifynoibinsssgeulrroolvisuentpdsisneiocnpfraevtitisiiveooonnlat(its6wse,ditpth7hee)r,TiofiyusncpstieehldleaI1We found that elevated ambientglucose increased the diabetes[6, 11, 12]

  • Oscillations in NADH andthe ATP/ADPratioare associated with the spontaneous oscillatory behavior of glycolysis that has been studied extensively in yeast cells and extracts [35,36,37,38], ascites cells [39], and heart [40] and skeletal muscle extracts (4146)

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Summary

Introduction

Insulin secretion in the intact organism, and by the in other cell types, because it is initiated by a change in fuel perfusedpancreas and groups of isolatedperifused metabolism rather than by the binding of an agonist to a islets, is pulsatile. We previouslyproposeda model for average cytosolic free Ca2+ level,the ATP/ADP ratio, glucose-stimulated insulin secretion based on oscillatory beand oxygenconsumption, as previouslyfound in havior of glycolysis [13,14,15,16]. Oscillatory patterns were ob- increased glycolytic flux in the islets due to increasegdlucose tained for Ca2+O, 2consumption, and insulin secretion concentration initiates oscillations gilnycolysis and the ATP/ in the presence of 10 and 20 mM glucose.

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