Peroxisome Proliferator-activated Receptor alpha Is Responsible for the Up-regulation of Hepatic Glucose-6-phosphatase Gene Expression in Fasting and db/db Mice

Abstract

Glucose-6-phosphatase (G6Pase) is a key enzyme that is responsible for the production of glucose in the liver during fasting or in type 2 diabetes mellitus (T2DM). During fasting or in T2DM, peroxisome proliferator-activated receptor alpha (PPAR alpha) is activated, which may contribute to increased hepatic glucose output. However, the mechanism by which PPAR alpha up-regulates hepatic G6Pase gene expression in these states is not well understood. We evaluated the mechanism by which PPAR alpha up-regulates hepatic G6Pase gene expression in fasting and T2DM states. In PPAR alpha-null mice, both hepatic G6Pase and phosphoenolpyruvate carboxykinase levels were not increased in the fasting state. Moreover, treatment of primary cultured hepatocytes with Wy14,643 or fenofibrate increased the G6Pase mRNA level. In addition, we have localized and characterized a PPAR-responsive element in the promoter region of the G6Pase gene. Chromatin immunoprecipitation (ChIP) assay revealed that PPAR alpha binding to the putative PPAR-responsive element of the G6Pase promoter was increased in fasted wild-type mice and db/db mice. These results indicate that PPAR alpha is responsible for glucose production through the up-regulation of hepatic G6Pase gene expression during fasting or T2DM animal models.