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Article
February 1965

"Double Barrel" Glucagon Test: Correlation With Enzyme Assays in Limit Dextrinosis

Author Affiliations

SEATTLE
From the Division of Endocrinology and Metabolic Diseases, Department of Pediatrics, University of Washington.

Am J Dis Child. 1965;109(2):162-164. doi:10.1001/archpedi.1965.02090020164014
Abstract

STRUCTURALLY, glycogen is a complex branched molecule composed of glucosyl units.1 The branching points are formed by 1,6-bonds, while all other glucosyl units are attached by 1,4-bonds. Liver phosphorylase, an enzyme activated by glucagon, splits the 1,4-bonds, releasing glucose-1-phosphate. This, in turn, is metabolized to glucose-6-phosphate and then to glucose. The debrancher enzyme (amylo-1,6-glucosidase) splits the 1,6-bonds; if this enzyme is deficient, the degradation of glycogen will cease at the branching points. Theoretically, a 14-hour fast in a patient with debrancher enzyme deficiency, type 3 glycogen storage disease by Cori's classification,1 would be associated with the degradation of the outer branches of glycogen by liver phosphorylase to the points of 1,6-bonds; glucagon administration to such a patient would not result in a hyperglycemic response. If, however, such a patient were fasted for 14 hours and then fed a regular meal, outer branches might be resynthesized sufficiently so

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