The physiological significance of pulsatile LHRH secretion in man: gonadotrophin responses to physiological doses of pulsatile versus continuous LHRH administration
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Authors
Gross, Kenneth M.
Bremner, William J.
Matsumoto, Alvin M.
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Blackwell Publishing
Abstract
This study tested whether pulsatile LHRH stimulation of the pituitary is
required for normal gonadotrophin secretion in man. Four men with
idiopathic hypogonadotrophic hypogonadism (IHH) and presumed endogenous
LHRH deficiency were taken off all hormonal replacement for 5-6 weeks,
then 5 micrograms LHRH was administered every 2 h for 1 week in order to
prime pituitary gonadotrophin responsiveness. A physiological dose of LHRH
(10 micrograms every 2 h) was then administered in both pulsatile and
continuous regimens, in varying order, to each man. Pulsatile LHRH was
capable of stimulating LH (as measured by bioassay) and FSH secretion,
while continuous administration of LHRH was not. Serum LH, measured by RIA
and bioassay, and FSH and free alpha-subunit levels, measured by RIA,
increased significantly (P less than 0.05) over pretreatment levels during
pulsatile LHRH administration. In contrast, bioactive LH and immunoactive
FSH did not change significantly compared to pretreatment values during
continuous infusion of the same total LHRH dose, although immunoactive LH
and free alpha-subunit levels did increase significantly (P less than
0.05). The ratio of LH bioactivity to immunoactivity was significantly
lower during the continuous compared to pulsatile LHRH regimen (P less
than 0.001). Similar serum LHRH levels were achieved during pulsatile and
continuous infusions. Serum testosterone and oestradiol levels did not
increase significantly from pretreatment levels during either regimen of
LHRH administration. It is concluded that a pulsatile LHRH signal pattern
is essential for normal pituitary gonadotrophin secretion in men with IHH.
Continuous infusion of a physiological dose of LHRH, which produced serum
LHRH levels which were indistinguishable from those found during pulsatile
administration, failed to stimulate FSH or bioactive LH secretion.
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Citation
Int J Androl. 1991 Feb;14(1):23-32
