Relation of Oxidation of Long‐Chain Fatty Acids to Gluconeogenesis in the Perfused Liver of the Guinea Pig:
- 1 June 1982
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 124 (3) , 465-470
- https://doi.org/10.1111/j.1432-1033.1982.tb06616.x
Abstract
The potent, specific inhibitor of long-chain fatty oxidation, 2-tetradecylglycidic acid (McN-3802), at 10 .mu.M totally abolished ketogenesis from endogenous substrates in the isolated perfused guinea pig liver. This effect was accompanied by a marked inhibition of gluconeogenesis from lactate plus pyruvate and by a shift toward a more oxidized state of the mitochondrial (3-hydroxybutyrate/acetoacetate ratio) and cytoplasmic (lactate/pyruvate ratio) compartments. The addition of octanoate (88-550 .mu.M) almost completely reversed the inhibitory effect of 2-tetradecylglycidic acid on gluconeogenesis. Octanoate oxidation, measured by the rate of ketogenesis, was not inhibited. This protective effect of octanoate against inhibition of gluconeogenesis by 2-tetradecylglycidic acid was seen even though in some experiments the mitochondrial redox state remained 2-3 times the magnitude observed prior to octanoate addition. Gluconeogenesis from 4 mM glycerol was not inhibited and gluconeogenesis from 4 mM propionate was only sightly inhibited by 2-tetradecylglycidic acid. Apparently, fatty acid oxidation in guinea pig liver is essential for maintaining maximal rates of gluconeogenesis, especially from substrates dependent on pyruvate carboxylation for conversion to glucose. A single dose of 2-tetradecylglycidic acid (orally, 10-25 mg/kg) given to guinea pigs previously fasted 72 h produced a highly significant decrease of total ketones, of the 3-hydroxybutyrate/acetoacetate ratio and of plasma glucose. A smaller hypoglycemic effect was seen when the drug was administered to animals fasted for only 24 or 48 h. It appears from evidence in vivo and in vitro that the guinea pig and rat respond similarly to inhibition of fatty acid oxidation. This may be important since it has been suggested that the role of fatty acid oxidation in glucose synthesis is markedly different in these 2 species.This publication has 22 references indexed in Scilit:
- Inhibition of mitochondrial carnitine palmitoyl transferase by 2-tetradecylglycidic acid (McN-3802) (Preliminary Communication)Life Sciences, 1980
- Gluconeogenesis in the Guinea Pig. Effect of Glucagon on Gluconeogenesis from Lactate by Isolated Perfused Guinea-Pig LiverEuropean Journal of Biochemistry, 1977
- On gluconeogenesis of human liverDiabetologia, 1976
- Acute Reversal of Experimental Diabetic Ketoacidosis in the Rat with (+)-DecanoylcarnitineJournal of Clinical Investigation, 1973
- Regulation of Gluconeogenesis in the Guinea Pig LiverEuropean Journal of Biochemistry, 1970
- The redox state of NAD+/NADH systems in guinea pig liver during increased fatty acid oxidationBiochimica et Biophysica Acta (BBA) - General Subjects, 1970
- The Role of Endogenous Lipid in Gluconeogenesis and Ketogenesis of Perfused Rat LiverEuropean Journal of Biochemistry, 1969
- Apparent Reversal of Insulin Resistance in Cardiac Muscle in Alloxan–Diabetes by 2-BromostearateNature, 1969
- Relation of fatty acid oxidation to gluconeogenesis: Effect of pentenoic acidLife Sciences, 1968
- Endogenous hepatic ketogenesis. Cofactor requirementsBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1967