Effect of obesity and feeding on the growth hormone (GH) response to the GH secretagogue L-692,429 in young men

被引:21
作者
Kirk, SE
Gertz, BJ
Schneider, SH
Hartman, ML
Pezzoli, SS
Wittreich, JM
Krupa, DA
Seibold, JR
Thorner, MO
机构
[1] UNIV VIRGINIA, HLTH SCI CTR, DEPT MED, DIV ENDOCRINOL & METAB, CHARLOTTESVILLE, VA 22908 USA
[2] UNIV MED & DENT NEW JERSEY, ROBERT WOOD JOHNSON MED SCH, NEW BRUNSWICK, NJ 08903 USA
[3] MERCK & CO INC, MERCK SHARP & DOHME RES LABS, RAHWAY, NJ 07065 USA
关键词
ANTERIOR-PITUITARY CELLS; FACTOR-I; SECRETION; HEXAPEPTIDE; RELEASE; INVITRO; SUPPRESSION; STIMULATION; BINDING; WOMEN;
D O I
10.1210/jc.82.4.1154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GH secretion and the response to GH secretagogues are significantly diminished in obese individuals. Previous studies have shown that L-692,429 (L), a nonpeptide mimetic of GH-releasing peptide, selectively stimulates GH release in normal young men and in the elderly, who also have diminished GH secretion. A paired, two-site study examined the effects of L on GR release in 12 healthy obese (part A; mean +/- sn: age, 26.1 +/- 3.3 yr; body mass index, 35.0 +/- 3.1 kg/m(2)) and 10 nonobese (part B; age, 22.2 +/- 2.3 yr; body mass index, less than or equal to 27.0) young men. In part A, placebo, low dose L (0.2 mg/kg), or high dose L (0.75 mg/kg) was administered iv over 15 min on 3 separate occasions after an overnight fast. Samples for GH, PRL, and cortisol determinations were obtained every 15 min. GH release (mean +/- se) was significantly increased by both doses of L compared to the effect of placebo: 12.6 +/- 1.8 mu g/L (low dose), 18.5 +/- 2.7 mu g/L (high dose), and 0.84 +/- 0.1 mu g/L (placebo), respectively (P < 0.05). In a subset of 6 obese men, in samples collected every 5 min, the GH response to both doses of L was significantly greater than that to 1 mu g/kg GHRH. To compare the response to low dose L in the obese and to determine the effects of feeding on this response, 0.2 mg/kg L was administered as described in part A to nonobese young men after an overnight fast (fasted) or a standardized breakfast (fed; part B). Low dose L was an effective GH secretagogue in nonobese young men; however, this effect was attenuated with feeding [43.6 +/- 7.9 (fasted) vs. 17.7 +/- 4.8 (fed)mu g/L]. Of note, the response to low dose L in fasted obese individuals was similar to that in fed nonobese individuals. The administration of L was well tolerated in both groups. We conclude that L is an effective GH secretagogue in obese and nonobese young men and may have therapeutic benefits when administered to relative (obese or elderly) or absolute GH-deficient individuals.
引用
收藏
页码:1154 / 1159
页数:6
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