OBJECTIVE: The reduction of spontaneous and stimulated growth hormone (GH)
secretion in obesity could reflect an increase of the inhibitory effect of
insulin growth factor I (IGF-l) on somatotroph secretion.
DESIGN: In the present study we aimed to verify the effect of low dose reco
mbinant human ICF-I (20 mug/kg subcutaneously (s.c.) at 0 min) on 3 h-spont
aneous GH secretion (mGHc, 0-180 min) and on the CH response to growth horm
one releasing hormone (GHRH) (1 mug/kg i.v. at + 180 min) in obesity.
SUBJECTS: Five obese women with abdominal adiposity (OB, age, mean +/- s.e.
m.: 31 +/- 7.13 y; BMI: 32.04 +/- 3.69 kg/m(2)) and eight age-matched lean
women (NW, 28.3 +/- 1.2y; 20.1 +/- 0.5 kg/m2) were studied.
RESULTS: The mGHc and GHRH-induced GH response in OB (1.0 +/- 0.7 mug/l; AU
C(180-270min): 688.6 +/- 202.4 mug/l min, respectively) were lower than in
NW (2.6 +/- 0.8 mug/l, 1315.9 +/- 189.9 mug/l min, respectively, P < 0.05).
The administration of rhlGF-I increased circulating IGF-I levels in OB and
NW to the same extent (339.0 +/- 50.39 and 420.3 +/- 30.5 mug/l, respectiv
ely). The rhlGF-I administration did not affect mGHe in OB or NW (1.1 +/- 0
.9 and 3.2 +/- 1.0 mug/l, respectively) but inhibited (P < 0.05) the CH res
ponse to GHRH in OB (324.2 +/- 153.1 mug/l) and NW (730.2 +/- 288.1 mug/l).
CONCLUSIONS: Our study shows that the administration of low dose rhlGF-I re
duces the somatotroph responsiveness to GHRH in obesity as well as in norma
l subjects.