Abstract
Removal of insulin-(131)I from plasma was studied in normal and diabetic subjects with both single injection and continuous infusion of isotope techniques. Patients were studied either in the fasting state or during steady-state hyperglycemia produced by a continuous intravenous glucose infusion. Steady-state plasma insulin concentration during these studies ranged from 10 to 264 muU/ml. Labeled insulin specific activity time curves consisted of more than one exponential, indicating that a multicompartmental system for insulin metabolism exists. A mathematical technique which is applicable to non-first order processes was used to calculate the rate at which insulin was lost irreversibly from the plasma insulin pool. A direct, linear relationship was found between insulin irreversible loss rate and plasma insulin concentration over the range of concentrations studied. This linearity implies lack of saturability of the insulin removal mechanism. Since the plasma insulin pool was in a steady state during these studies, insulin irreversible loss rate was equal to the rate at which newly secreted insulin was being delivered to the general circulation. Therefore, these results indicate that changes in plasma insulin concentration result from parallel changes in the rate of insulin delivery and not from changes in the opposite direction of the rate of insulin removal. A wide range of insulin delivery rates was found among patients with similar plasma glucose concentrations, suggesting that there exists considerable variability in responsiveness to endogenous insulin among these patients.
MeSH Terms
Adult
Aged
Blood Glucose/analysis
Diabetes Mellitus/blood,metabolism
Fasting
Female
Glucose Tolerance Test
Humans
Hyperglycemia
Infusions, Parenteral
Insulin/blood,metabolism
Insulin Secretion
Iodine Isotopes
Male
Middle Aged
Models, Theoretical
Chemicals
Blood Glucose
Insulin
Iodine Isotopes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Stern M P
Farquhar J W
Silvers A
Reaven G M
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24 references, click to expand
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