Literature DB >> 8760089

Effects of pulsatile delivery of basal growth hormone on lipolysis in humans.

E Cersosimo1, F Danou, M Persson, J M Miles.   

Abstract

Growth hormone (GH) excess stimulates lipolysis, but its role in the hierarchy of lipolysis regulation is not clear. We studied whether pulsatile GH delivery is required for its lipolytic effect. With use of the pancreatic clamp, eight subjects were randomized to three protocols: protocol A, GH deficiency; protocol B, constant GH infusion; protocol C, pulsatile GH delivery (same total GH as protocol B). Pulsatile GH was given in four consecutive bursts, with symmetric peak width (60 min), amplitude of 10.7 (men) and 15 (women) ng.kg-1.min-1, and peak width at half-height of 15 min. Palmitate flux (PF) was measured at baseline and in the last hour of each study with [3H]palmitate. GH (ng/ml) decreased from approximately 3.5 to 2.0 in protocol A (P < 0.05), it remained between 3.2 and 4.0 in protocol B (P < 0.05), but in protocol C it fluctuated between approximately 2.7 and approximately 5.0 (P < 0.05). Palmitate concentration (in mumol/l) was approximately 150 at baseline; it did not change in protocols A and B (137 +/- 17 and 136 +/- 12, respectively) but increased to 198 +/- 16 (P < 0.05) in protocol C. PF (mumol.kg-1.min-1) was approximately 2.7 at baseline and did not change in protocol B (2.4 +/- 0.2); it decreased to 2.2 +/- 0.1 in protocol A (P < 0.05); it increased to 3.1 +/- 0.3 (P < 0.05) in protocol C. These experiments provide evidence that pulsatile secretion of GH is required for its lipolytic effect.

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Year:  1996        PMID: 8760089     DOI: 10.1152/ajpendo.1996.271.1.E123

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  14 in total

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2.  Dynamic testosterone responses to near-physiological LH pulses are determined by the time pattern of prior intravenous LH infusion.

Authors:  Johannes D Veldhuis; Peter Y Liu; Paul Y Takahashi; Daniel M Keenan
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3.  Rapid suppression of growth hormone concentration by overeating: potential mediation by hyperinsulinemia.

Authors:  Andrea S Cornford; Ariel L Barkan; Jeffrey F Horowitz
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4.  Suppression in growth hormone during overeating ameliorates the increase in insulin resistance and cardiovascular disease risk.

Authors:  Andrea S Cornford; Ariel L Barkan; Alexander Hinko; Jeffrey F Horowitz
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Review 5.  Effects of growth hormone-releasing hormone on visceral fat, metabolic, and cardiovascular indices in human studies.

Authors:  Takara L Stanley; Steven K Grinspoon
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6.  Basal, but not pulsatile, growth hormone secretion determines the ambient circulating levels of insulin-like growth factor-I.

Authors:  Alexander T Faje; Ariel L Barkan
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7.  Effects of a growth hormone-releasing hormone analog on endogenous GH pulsatility and insulin sensitivity in healthy men.

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9.  Role of growth hormone in regulating lipolysis, proteolysis, and hepatic glucose production during fasting.

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10.  The pattern of growth hormone delivery to peripheral tissues determines insulin-like growth factor-1 and lipolytic responses in obese subjects.

Authors:  Sowmya Surya; Jeffrey F Horowitz; Naila Goldenberg; Alla Sakharova; Matthew Harber; Andrea S Cornford; Kathy Symons; Ariel L Barkan
Journal:  J Clin Endocrinol Metab       Date:  2009-05-26       Impact factor: 5.958

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