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Am J Physiol Regul Integr Comp Physiol 286: R206-R216, 2004. First published September 25, 2003; doi:10.1152/ajpregu.00340.2003
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APPETITE, OBESITY AND METABOLISM

Regulation of hepatic glucose metabolism by leptin in pig and rat primary hepatocyte cultures

Priya Raman, Shawn S. Donkin, and Michael E. Spurlock

Department of Animal Sciences, Comparative Medicine Program, Purdue University, West Lafayette, Indiana 47907-1151

Submitted 20 June 2003 ; accepted in final form 25 August 2003

Direct effects of leptin on gluconeogenesis in rat hepatocytes are equivocal, and model systems from other species have not been extensively explored in assessing the regulation of glucose metabolism by leptin. Therefore, the goal of the present study was to compare the effects of leptin on gluconeogenesis in pig and rat hepatocyte cultures as well as to investigate an underlying mechanism of action at the level of phosphoenolpyruvate carboxykinase (PEPCK). In rat hepatocytes, leptin exposure (3 h, 50 and 100 nM) attenuated glucagon-stimulated hepatic gluconeogenesis by 35 and 38% (P < 0.05), respectively. However, leptin did not produce any significant acute effect in pig hepatocytes. Leptin exposure for 24 h failed to produce any significant effect on gluconeogenesis in either rat or pig hepatocytes cultured in the presence of glucagon or dexamethasone. Mechanistically, there was a 25-35% decrease (P < 0.05) in glucagon-induced PEPCK mRNA levels in rat but not pig hepatocytes cultured with leptin. This effect on PEPCK mRNA was not due to an alteration in the relative abundance of the leptin receptor or the ability of PEPCK to respond to cAMP. The nonuniformity of the effects of leptin on gluconeogenesis in pig and rat hepatocytes indicates differences in leptin action between species. Furthermore, the unique action of leptin in porcine hepatocytes points to the utility of this model system for biomedical research and also underscores the value of comparative studies.

hepatocytes; phosphoenolpyruvate carboxykinase; receptor



Address for reprint requests and other correspondence: M. E. Spurlock, Purdue Univ., Lilly Hall of Life Sciences, 915 West State St., West Lafayette, IN 47907 (E-mail: spurloc0{at}purdue.edu).




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