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Research Article Free access | 10.1172/JCI109156

Glucose-Stimulated 45Calcium Efflux from Isolated Rat Pancreatic Islets

Barbara J. Frankel, Walter T. Imagawa, Michael D. L. O'Connor, Ingmar Lundquist, John A. Kromhout, Rudolph E. Fanska, and Gerold M. Grodsky

Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Metabolic Research Unit and the Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143

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Published September 1, 1978 - More info

Published in Volume 62, Issue 3 on September 1, 1978
J Clin Invest. 1978;62(3):525–531. https://doi.org/10.1172/JCI109156.
© 1978 The American Society for Clinical Investigation
Published September 1, 1978 - Version history
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Abstract

Kinetics of 45Ca efflux and insulin release were studied in collagenase-isolated rat islets during 2-h perifusions with calcium-depleted (0.05 mM) bicarbonate-phosphate buffer containing 2.2 mM glucose. Addition of glucose (16.7 mM) suppressed 45Ca efflux by 30%. Removal of glucose caused an “off response” of insulin release. The perifusion of a normal concentration of Ca (2.3 mM) greatly stimulated 45Ca efflux, indicating Ca ↔ 45Ca exchange. When Ca and glucose were superimposed, the effects on 45Ca efflux and insulin release depended upon the order of presentation of the stimuli: when Ca was added to an ongoing 16.7-mM glucose perifusion, biphasic patterns of 45Ca and insulin release were seen; when glucose was superimposed on a Ca perifusion, an inhibition of the Ca-stimulated 45Ca efflux occurred, and a reduced but clearly biphasic insulin response was seen. The subsequent insulin off response after with-drawal of the glucose was also reduced.

Mathematical “peeling” of 45Ca efflux curves from unstimulated islets suggests that there are at least two, and probably three, different intracellular Ca compartments (not including the extracellular sucrose space). At the beginning of perifusion, these three compartments (I, II, III) contain 25, 56, and 19% of the intracellular 45Ca, and their rates of efflux are 6.7, 1.2, and 0.1%/min, respectively. Glucose appears to suppress efflux from the largest compartment (II); Ca appears to exchange with 45Ca from a more inert compartment (III). The relationship between insulin and 45Ca release is not stoichiometric.

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