Endocrine Abstracts

Background: Microsomal glucose-6-phosphatase-alpha (G6Pase-alpha) and glucose-6-phosphate transporter (G6PT) perform the terminal step in both glycogenolysis and gluconeogenesis. Deficiency of G6Pase-alpha leads to glycogen storage disease type 1a, whereas deficiency of G6PT leads to glycogen storage disease type 1b. Partial inhibition of G6Pase in rats results in increased hepatic triglyceride contents and de novo lipogenesis leading to hepatic steatosis. Hepatic steat...