Selective tonic inhibition of G-6-Pase catalytic subunit, but not G-6-P transporter, gene expression by insulin in vivo

LA Hornbuckle, DS Edgerton… - American Journal …, 2001 - journals.physiology.org
LA Hornbuckle, DS Edgerton, JE Ayala, CA Svitek, JK Oeser, DW Neal, S Cardin…
American Journal of Physiology-Endocrinology and Metabolism, 2001journals.physiology.org
The regulation of glucose-6-phosphatase (G-6-Pase) catalytic subunit and glucose 6-
phosphate (G-6-P) transporter gene expression by insulin in conscious dogs in vivo and in
tissue culture cells in situ were compared. In pancreatic-clamped, euglycemic conscious
dogs, a 5-h period of hypoinsulinemia led to a marked increase in hepatic G-6-Pase catalytic
subunit mRNA; however, G-6-P transporter mRNA was unchanged. In contrast, a 5-h period
of hyperinsulinemia resulted in a suppression of both G-6-Pase catalytic subunit and G-6-P …
The regulation of glucose-6-phosphatase (G-6-Pase) catalytic subunit and glucose 6-phosphate (G-6-P) transporter gene expression by insulin in conscious dogs in vivo and in tissue culture cells in situ were compared. In pancreatic-clamped, euglycemic conscious dogs, a 5-h period of hypoinsulinemia led to a marked increase in hepatic G-6-Pase catalytic subunit mRNA; however, G-6-P transporter mRNA was unchanged. In contrast, a 5-h period of hyperinsulinemia resulted in a suppression of both G-6-Pase catalytic subunit and G-6-P transporter gene expression. Similarly, insulin suppressed G-6-Pase catalytic subunit and G-6-P transporter gene expression in H4IIE hepatoma cells. However, the magnitude of the insulin effect was much greater on G-6-Pase catalytic subunit gene expression and was manifested more rapidly. Furthermore, cAMP stimulated G-6-Pase catalytic subunit expression in H4IIE cells and in primary hepatocytes but had no effect on G-6-P transporter expression. These results suggest that the relative control strengths of the G-6-Pase catalytic subunit and G-6-P transporter in the G-6-Pase reaction are likely to vary depending on the in vivo environment.
American Physiological Society