TY - JOUR
T1 - Effects of pulsatile delivery of basal growth hormone on lipolysis in humans
AU - Cersosimo, Eugenio
AU - Danou, Fotini
AU - Persson, Mai
AU - Miles, John M.
PY - 1996/12/1
Y1 - 1996/12/1
N2 - 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 -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 -2.7 and -5.0 (P < 0-05). Palmitate concentration (in μmol/1) was -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 (ng·kg-1 ·min-1) was -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.
AB - 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 -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 -2.7 and -5.0 (P < 0-05). Palmitate concentration (in μmol/1) was -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 (ng·kg-1 ·min-1) was -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.
KW - Fat metabolism
KW - Free fatty acids
KW - Oscillatory secretion
KW - Palmitate
KW - Somatotropin
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M3 - Article
AN - SCOPUS:33745341848
SN - 0002-9513
VL - 271
SP - E127-E137
JO - American Journal of Physiology
JF - American Journal of Physiology
IS - 1 PART 1
ER -