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http://purl.uniprot.org/citations/19046568http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19046568http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19046568http://www.w3.org/2000/01/rdf-schema#comment"Glucagon receptor (Gcgr) signaling maintains hepatic glucose production during the fasting state; however, the importance of the Gcgr for lipid metabolism is unclear. We show here that fasted Gcgr-/-mice exhibit a significant increase in hepatic triglyceride secretion and fasting increases fatty acid oxidation (FAO) in wild-type (WT) but not in Gcgr-/-mice. Moreover fasting upregulated the expression of FAO-related hepatic mRNA transcripts in Gcgr+/+ but not in Gcgr-/-mice. Exogenous glucagon administration reduced plasma triglycerides in WT mice, inhibited TG synthesis and secretion, and stimulated FA beta oxidation in Gcgr+/+ hepatocytes. The actions of glucagon on TG synthesis and FAO were abolished in PPARalpha-/-hepatocytes. These findings demonstrate that the Gcgr receptor is required for control of lipid metabolism during the adaptive metabolic response to fasting."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.org/dc/terms/identifier"doi:10.1016/j.cmet.2008.09.008"xsd:string
http://purl.uniprot.org/citations/19046568http://purl.org/dc/terms/identifier"doi:10.1016/j.cmet.2008.09.008"xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Maziarz M."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Maziarz M."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Charron M.J."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Charron M.J."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Drucker D.J."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Drucker D.J."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Maida A."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Maida A."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Baggio L.L."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Baggio L.L."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Longuet C."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Longuet C."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Sinclair E.M."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/author"Sinclair E.M."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/name"Cell Metab."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/name"Cell Metab."xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/pages"359-371"xsd:string
http://purl.uniprot.org/citations/19046568http://purl.uniprot.org/core/pages"359-371"xsd:string