Læknablaðið : fylgirit - 01.06.1982, Qupperneq 38

Læknablaðið : fylgirit - 01.06.1982, Qupperneq 38
25 UTILIZATION OF THE ARTIFICIAL PANCREAS IN THE STUDY OF THE POTENCY OF SEMI-SYNTHETIC HUMAN INSULIN IN TYPE I DIABETICS. AA. PRANGE HANSEN, 0. SCHMITZ, S.E. CHRISTENSEN, H. 0RSKOV and L. HEDING: First and Second University Clinic of Internal Medicine, Kommu- nehospitalet, Aarhus and NOVO Research Institute, Bagsværd, Den- mark. The aim of the present study was to compare the efficacy of se- mi-synthetic human insulin (Novo) and porcine insulin in juve- nile diabetics ^sing a glucose controlled insulin infusion sy- stem (BiostatorK). Two types of experiments were performed. 1. Comparison of 24-hour insulin requirements: After stabiliza- tion of the blood glucose level at 80 mg/100 ml four diabe- tics were treated during two 24-hours periods in a randomized succession with human or porcine insulin. The set constants selected for the algorithms (KR = 70, KF = 67, QI = 40) mini- mizes insulin delivery. Diurnal blood glucose levels (98.1 - 2.8 mg/100 ml and 99.0 - 2.5 mg/100 ml) and diurnal insulin requirements (47658 - 3494 mU and 47550 - 3733 mU) were iden- tical in the two regimens and the counter-regulatory hormones did not differ. 2. Comparison of the glucose lowering., effect after IV glucose: After stabilization of the blood glucose level at 80 mg/100 ml for hours six diabetics received 0.5 g glucose/kg body weight iv over 3 min. on two separate days. Following the glucose load human or porcine insulin were given at a con- stant rate of 1 mU/kg body weight/min. The fall in blood glu- cose was rectilinaar and the regression lines were superim- posable in everv individual diabetic. The slopes (-1.15 - J.10 and -1.16 - 0.09) and the regression coefficients (0.998 - 0.001 and 0.996 - 0.001 ) were identical in the two regimens,. Other experiments have shown that this method is able to de- monstrate a difference in potency of 10 per cent. In conclusion: IV administrated semi-synthetic human and porcine insulin have identical effects on the blood glucose in insulin- dependent diabetics.
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