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Research Article Free access | 10.1172/JCI106307

The effect of fasting, diet, and actinomycin D on insulin secretion in the rat

N. J. Grey, S. Goldring, and D. M. Kipnis

1Metabolism Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

Find articles by Grey, N. in: PubMed | Google Scholar

1Metabolism Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

Find articles by Goldring, S. in: PubMed | Google Scholar

1Metabolism Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

Find articles by Kipnis, D. in: PubMed | Google Scholar

Published May 1, 1970 - More info

Published in Volume 49, Issue 5 on May 1, 1970
J Clin Invest. 1970;49(5):881–889. https://doi.org/10.1172/JCI106307.
© 1970 The American Society for Clinical Investigation
Published May 1, 1970 - Version history
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Abstract

The present studies were performed to elucidate the mechanisms responsible for the impairment of glucose-stimulated insulin secretion observed in fasting. Rats fasted for 48 hr displayed marked impairment in their insulin secretory response to both oral and intravenous glucose. Glucose-stimulated insulin secretion was restored within 24 hr by refeeding; actinomycin D given before refeeding blocked the expected return of normal glucose-stimulated insulin secretion despite adequate food intake. Fasted rats refed a diet devoid of carbohydrate failed to display a return of normal insulin secretory responsiveness to oral glucose in contrast to rats fed isocalorically a high carbohydrate diet. Differences in insulin secretion in fed, fasted, and fasted-refed rats could not be attributed to changes in pancreatic insulin content. There was no significant difference in the insulin secretory response to aminophylline of fed, fasted, or fasted-refed rats. The intermittent pulsing of fasted rats with hyperglycemic episodes by the injection of small amounts of glucose (500 mg) intraperitoneally every 8 hr ameliorated the impairment of glucose-stimulated insulin secretion characteristic of the fasting state. These results suggest that the impairment of glucose-stimulated insulin secretion during fasting and its restoration by refeeding are regulated by changes in a glucose-inducible enzyme system in the pancreatic beta cell.

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