[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address Please contact the publisher to request reinstatement.
[Skip to Content Landing]
March 1969

Insulin-Glucose Dispersion and Interaction SystemLiver Control Mechanisms

Author Affiliations

Rochester, NY; Richland, Wash

From the Department of Medicine, University of Rochester School of Medicine and Dentistry (Dr. Izzo), University of Rochester, Rochester, NY, and the Pacific; Northwest Laboratory, Battelle Memorial Institute (Dr. Bartlett), Richland, Wash.

Arch Intern Med. 1969;123(3):272-283. doi:10.1001/archinte.1969.00300130054009

Data on the disposition of insulin I 131 are reviewed and analyzed to determine the mechanisms responsible for insulin dispersion phenomena. The liver is indicated as the primary organ responsible for controlling plasma clearance rates by the following two methods: chemical reaction that degrades intact insulin supplied by the plasma, and the presence of a region that controls the rate at which insulin I 131 is made available to the reaction sites. The degradation reaction is apparently second order with respect to intact insulin I 131, so that combination of two insulin I 131 molecules with insulin glutathione transhydrogenase appears to be required for degradation to occur. A proposed model describing the insulin and glucose dispersion systems and the interaction between them is capable of explaining qualitatively how plasma insulin and glucose levels are maintained.