Horm Metab Res 1986; 18(7): 466-469
DOI: 10.1055/s-2007-1012347
Clinical

© Georg Thieme Verlag, Stuttgart · New York

Fasting and Feeding Variations of Insulin Requirements and Insulin Binding to Erythrocytes at Different Times of the Day in Insulin Dependent Diabetics - Assessed Under the Condition of Glucose-Controlled Insulin Infusion

C.-T. Hung, J. Beyer, G. Schulz
  • Abteilung für Innere Medizin, Endokrinologie und Stoffwechsel, Universität Mainz, Mainz, Germany
Further Information

Publication History

1984

1985

Publication Date:
14 March 2008 (online)

Summary

Nine insulin-dependent diabetic patients were examined for insulin requirement, counterregulatory hormones, and receptor binding during their connection to glucose-controlled insulin infusion system. They were of 103% ideal body weight. A diet of 45% carbohydrate, 20% protein and 35% fat was divided into three meals and three snacks, averaging the dailycalorie intake of 1859 kcal. Following an equilibrating phase of 14 hours after the connection to the glucose-controlled insulin infusion system the blood samples were taken at 0800, 1200 and 1800. The insulin infusion rate increased at 0300 in the early morning from 0.128 mU/kg/min to 0.221 mU/kg/min (P < 0.02). The postprandial insulin infusion rate jumped from 0.7 U/h (0700-0800) to 7.5 U/h (0800-0900). The calorie related and carbohydrate related insulin demands after breakfast were also highest and declined after lunch respectively (1.16 uU/kg/min kj vs. 0.61 uU/kg/min kj, P < 0.05 and 236 mU/g CHO vs. 129 mU/g CHO and 143 mU/g CHO). Of the counterregulatory hormones the cortisol showed a significant diurnal rhythm to insulin demands. The insulin tracer binding was higher at 0800 before breakfast than that at 1200 before lunch (P < 0.05). The increased binding could be better attributed to receptor concentration change than to affinity change. The cause of insulin relative insensitivity in the morning could be due to altered liver response to the cortisol peak in type 1 diabetics. The preserved variation of insulin binding in our patients might be referred to feeding.