| Literature DB >> 23606725 |
Berthil F F Clasen1, Thomas Krusenstjerna-Hafstrøm, Mikkel Holm Vendelbo, Kasper Thorsen, Carlos Escande, Niels Møller, Steen B Pedersen, Jens Otto L Jørgensen, Niels Jessen.
Abstract
Growth hormone (GH) acutely stimulates lipolysis and fat oxidation, a process that operates postabsorptively and involves activation of the JAK-STAT pathway in the target tissue; no in vivo data exist regarding subsequent GH-regulated gene transcription. We obtained serum samples and muscle biopsies in human subjects before and 2 h after administration of a GH bolus. A significant (~75%) elevation in serum FFA levels was recorded post GH. Microarray identified 79 GH-regulated genes in muscle. With qRT-PCR, we then examined the expression of selected genes in the presence and absence of glucose-induced suppression of lipolysis. Four genes involved in the JAK-STAT5 signaling pathway were regulated by GH, including SOCS1-3 and CISH, in addition to three genes associated with insulin action: NFκB1A, PIK3C2B, and PRKAG2. The gene encoding ANGPTL4, a protein involved in lipolysis and suppression of LPL activity, exhibited the most pronounced upregulation (5.6-fold) after GH, which was abrogated by concomitant suppression of lipolysis. Therefore, the GH-induced stimulation of ANGPTL4 gene expression seems secondary to induction of lipolysis. This new concept implies that abundant supply of circulating FFA decreases the need for alternative triglyceride-derived FFA through distinct inhibition of LPL mediated by increased ANGPTL4 gene expression in human muscle.Entities:
Keywords: angiopoietin-related protein-like 4; growth hormone; human gene array; lipid metabolism
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Year: 2013 PMID: 23606725 PMCID: PMC3679400 DOI: 10.1194/jlr.P034520
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922