Key result
Acute IV GH upregulates skeletal muscle ANGPTL4 expression ~5.6-fold, an effect blocked by lipolysis suppression.
Why the study?
No in vivo data exist regarding GH-regulated gene transcription in human skeletal muscle after acute GH administration.
Does an acute intravenous GH bolus alter gene expression in skeletal muscle in human subjects?
Does an acute intravenous GH bolus alter gene expression in skeletal muscle in human subjects?
Effect estimate: 5.6-fold upregulation
GH-induced stimulation of ANGPTL4 gene expression in human skeletal muscle appears secondary to the induction of lipolysis, suggesting a mechanism for regulating triglyceride-derived FFA.
Acute GH regulates 79 muscle genes in humans; hypothesis-generating for lipolysis mechanisms, should not yet change practice.
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.
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Clasen et al. (2013) studied this question. Intravenous GH bolus vs. Baseline (before administration) was evaluated on ANGPTL4 gene expression in skeletal muscle (5.6-fold upregulation). An acute intravenous GH bolus in human subjects induced a 5.6-fold upregulation of ANGPTL4 gene expression in skeletal muscle, an effect abrogated by concomitant suppression of lipolysis.
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