Two-Month Treatment of Obese Subjects with the Oral Growth Hormone (GH) Secretagogue MK-677 Increases GH Secretion, Fat-Free Mass, and Energy Expenditure1
ABSTRACT Obesity is associated with blunted GH secretion, unfavorable body composition, and increased cardiovascular mortality. The objective of this study was to investigate the effects of oral treatment with the GH secretagogue MK-677 on GH secretion and body composition in otherwise healthy obese...
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Veröffentlicht in: | The journal of clinical endocrinology and metabolism 1998-02, Vol.83 (2), p.362-369 |
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Sprache: | eng |
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Zusammenfassung: | ABSTRACT
Obesity is associated with blunted GH secretion, unfavorable body
composition, and increased cardiovascular mortality. The objective of
this study was to investigate the effects of oral treatment with the GH
secretagogue MK-677 on GH secretion and body composition in otherwise
healthy obese males. The study was randomized, double blind, parallel,
and placebo controlled. Twenty-four obese males, aged 18–50 yr, with
body mass indexes greater than 30 kg/m2 and waist/hip
ratios greater than 0.95, were treated with MK-677 25 mg (n = 12)
or placebo (n = 12) daily for 8 weeks.
Serum insulin-like growth factor I (IGF-I) increased approximately 40%
with MK-677 treatment (P < 0.001
vs. placebo). Serum IGF-binding protein-3 was also
significantly increased (P ≤ 0.001
vs. placebo). GH and PRL (peak and area under the curve
values) were significantly increased after the initial dose of MK-677.
Significant increases, with the exception of peak PRL, persisted at 2
and 8 weeks of treatment. The increases in GH and PRL after the initial
dose were significantly greater than the increase seen after multiple
doses. Serum and urinary concentrations of cortisol were not increased
at 2 and 8 weeks (P = NS, vs.
placebo). Fat-free mass increased significantly in the MK-677 treatment
group when determined with dual energy x-ray absorptiometry
(P < 0.01) or using a four-compartment model
(P < 0.05). Total and visceral fat were not
significantly changed with active therapy. The basal metabolic rate was
significantly increased at 2 weeks of MK-677 treatment
(P = 0.01) but not at 8 weeks
(P = 0.1). Fasting concentrations of glucose and
insulin were unchanged, whereas an oral glucose tolerance test showed
impairment of glucose homeostasis at 2 and 8 weeks.
We conclude that 2-month treatment with MK-677 in healthy obese males
caused a sustained increase in serum levels of GH, IGF-I, and
IGF-binding protein-3. The effects on cortisol secretion were
transient. Changes in body composition and energy expenditure were of
an anabolic nature, with a sustained increase in fat-free mass and a
transient increase in basal metabolic rate. Further studies are needed
to evaluate whether a higher dose of MK-677 or a more prolonged
treatment period can promote a reduction in body fat. |
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ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.83.2.4539 |