Ca. Jaffe et al., REGULATORY MECHANISMS OF GROWTH-HORMONE SECRETION ARE SEXUALLY DIMORPHIC, The Journal of clinical investigation, 102(1), 1998, pp. 153-164
Sexually dimorphic growth hormone (GH) secretory pattern is important
in the determination of gender-specific patterns of growth and metabol
ism in rats. Whether GH secretion in humans is also sexually dimorphic
and the neuroendocrine mechanisms governing this potential difference
are not fully established. We have compared pulsatile GH secretion pr
ofiles in young men and women in the baseline state and during a conti
nuous intravenous infusion of recombinant human insulin-like growth fa
ctor I (rhIGF-I), During the baseline study, men had large nocturnal G
H pulses and relatively small pulses during the rest of the day, In co
ntrast, women had more continuous GH secretion and more frequent GH pu
lses that were of more uniform size. The infusion of rhIGF-I (10 mu g/
kg/h) potently suppressed both spontaneous and growth hormone-releasin
g hormone (GHRH)-induced GH secretion in men. In women, however, rhIGF
-I had less effect on pulsatile GH secretion and did not suppress the
GH response to GHRH. These data demonstrate the existence of sexual di
morphism in the regulatory mechanisms involved in GH secretion in huma
ns. The persistence of GH responses to GHRH in women suggests that neg
ative feedback by IGF-I might be expressed, in part, through suppressi
on of hypothalamic GHRH.