Multiple requirements for glycogen synthesis by hepatocytes isolated from fasted rats

• Published in: The Journal of biological chemistry 1985-11, Vol.260 (27), p.14683-14688
• Main Authors: Chen, K S, Lardy, H A
• Format: Article
• Language: English
• Subjects: Amino Acids, Branched-Chain - pharmacology; Animals; Biological and medical sciences; Cell metabolism, cell oxidation; Cell physiology; Cycloheximide - pharmacology; Deoxyglucose - pharmacology; Dihydroxyacetone - pharmacology; Fasting; Fundamental and applied biological sciences. Psychology; Glucose - pharmacology; In Vitro Techniques; Kinetics; Lactates - pharmacology; Lactic Acid; Liver - drug effects; Liver - metabolism; Liver Glycogen - biosynthesis; Male; Molecular and cellular biology; Puromycin - pharmacology; Pyruvates - pharmacology; Pyruvic Acid; Rats; Rats, Inbred Strains
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)38625-8

Glycogen synthesis from various combinations of substrates by hepatocytes isolated from rats fasted 24 h was studied. As reported by Katz et al. (Katz, J., Golden, S., and Wals, P. A. (1976) Proc. Natl. Acad. Sci. U. S. A. 73, 3433-3437), appreciable rates of glycogen synthesis occurred only in the presence of gluconeogenic precursors and one of several amino acids, which includes L-glutamine. L-Leucine had negligible effects on glycogen synthesis from 20 mM dihydroxyacetone and/or 15 mM glucose when L-glutamine was not added to the medium. In the presence of 10 mM L-glutamine, L-leucine greatly increased glycogen synthesis from these substrates. alpha-Ketoisocaproate was ineffective, as was oleate. NH4Cl depressed glycogen synthesis from 10 mM glucose plus 20 mM dihydroxyacetone in the absence of added L-glutamine and enhanced that in its presence, but these effects were weak compared to those of L-leucine. The amino acid analogues L-norvaline and L-norleucine exerted effects that were similar to those exerted by L-leucine. Under all conditions studied, cycloheximide and puromycin inhibited net glycogen synthesis. Cycloheximide did not stimulate gluconeogenesis from dihydroxyacetone, or phosphorylase in hepatocytes from starved rats, or glycogenolysis in hepatocytes from fed rats. Puromycin, however, stimulated glycogenolysis in hepatocytes from fed rats. Glycogen synthesis from 20 mM dihydroxyacetone proceeds with a pronounced initial lag phase that can be shortened by incubation of cells with glutamine plus leucine before addition of dihydroxyacetone. Concurrent measurements of glycogen synthesis, glycogen synthase, and gluconeogenesis under different conditions reveal that in addition to protein synthesis, activation of glycogen synthase, which must occur to allow glycogen synthesis in hepatocytes, requires a second component which can be satisfied by addition of dihydroxyacetone or fructose to the cells.