Upregulation of hepatic glucose 6-phosphatase gene expression in rats treated with an inhibitor of glucose-6-phosphate translocase.

Abstract

The multicomponent hepatic glucose 6-phosphatase (Glc-6-Pase) system catalyzes the terminal step of hepatic glucose production and plays a key role in the regulation of blood glucose. We used the chlorogenic acid derivative S 3483, a reversible inhibitor of the glucose-6-phosphate (Glc-6-P) translocase component, to demonstrate for the first time upregulation of Glc-6-Pase expression in rat liver in vivo after inhibition of Glc-6-P translocase. In accordance with its mode of action, S 3483-treatment of overnight-fasted rats induced hypoglycemia and increased blood lactate, hepatic Glc-6-P, and glycogen. The metabolic changes were accompanied by rapid and marked increases in Glc-6-Pase mRNA (above 35-fold), protein (about 2-fold), and enzymatic activity (about 2-fold). Maximal mRNA levels were reached after 4 h of treatment. Glycemia, blood lactate, and Glc-6-Pase mRNA levels returned to control values, whereas Glc-6-P and glycogen levels decreased but were still elevated 2 h after S 3483 withdrawal. The capacity for Glc-6-P influx was only marginally increased after 8.5 h of treatment. Prevention of hypoglycemia by euglycemic clamp did not abolish the increase in Glc-6-Pase mRNA induced by S 3483 treatment. A similar pattern of hypoglycemia and possibly of associated counterregulatory responses elicited by treatment with the phosphoenolpyruvate carboxykinase inhibitor 3-mercaptopicolinic acid could account for only a 2-fold induction of Glc-6-Pase mRNA. These findings suggest that the significant upregulation of Glc-6-Pase gene expression observed after treatment of rats in vivo with an inhibitor of Glc-6-P translocase is caused predominantly either by S 3483 per se or by the compound-induced changes of intracellular carbohydrate metabolism.

• Authors: C Simon, A W Herling, G Preibisch, H J Burger
• Journal: Archives of biochemistry and biophysics (Arch Biochem Biophys) Vol. 373 Issue 2 Pg. 418-28 (Jan 15 2000) ISSN: 0003-9861 [Print] United States
• PMID: 10620367 (Publication Type: Journal Article)
• Copyright: Copyright 2000 Academic Press.

Chemical References

• Antiporters
• Blood Glucose
• Cyclohexanecarboxylic Acids
• Enzyme Inhibitors
• Monosaccharide Transport Proteins
• Picolinic Acids
• RNA, Messenger
• S 3483
• Slc37a4 protein, rat
• glucose 6-phosphate(transporter)
• 3-mercaptopicolinic acid
• Phosphotransferases
• Glucose-6-Phosphatase

Topics

• Animals
• Antiporters
• Blood Glucose (metabolism)
• Cyclohexanecarboxylic Acids (pharmacology)
• Enzyme Inhibitors (pharmacology)
• Gene Expression Regulation, Enzymologic (drug effects)
• Glucose Clamp Technique
• Glucose-6-Phosphatase (biosynthesis, genetics)
• Hypoglycemia (metabolism)
• Kinetics
• Liver (drug effects, enzymology)
• Male
• Microsomes, Liver (enzymology)
• Monosaccharide Transport Proteins
• Phosphotransferases (antagonists & inhibitors)
• Picolinic Acids (pharmacology)
• RNA, Messenger (metabolism)
• Rats
• Rats, Wistar
• Up-Regulation