Testosterone administration inhibits gonadotropin secretion by an effect directly on the human pituitary
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Bremner, William J.
Sheckter, Carol B.
Matsumoto, Alvin M.
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Endocrine Society
Abstract
Testosterone (T) administration slows LH pulse frequency in man,
presumably by an effect on the hypothalamic GnRH pulse generator, but it
also may have a direct action on the pituitary. To determine if T does
indeed affect gonadotropin secretion by acting directly on the pituitary,
we studied the effect of T on GnRH-stimulated gonadotropin secretion. Six
men with hypogonadotropic hypogonadism were treated with physiological
doses of GnRH (5 micrograms every 2 h, sc by automatic infusion pump) for
6 weeks. Once their gonadotropin levels were normal, the men received a
supraphysiological dosage of T enanthate (200 mg, im, weekly for 8 weeks)
in addition to GnRH. They then received GnRH alone for a final 8-week
period. Blood sampling was performed every 10 min for 8 h at the end of
each of the three study periods. T administration suppressed the mean
serum LH level to about 50% of the value during GnRH alone [18 +/- 2 (+/-
SE) vs. 37 +/- 2 micrograms/L; P less than 0.05] and suppressed the mean
serum FSH level to about 30% of the value during GnRH alone (39 +/- 6 vs.
128 +/- 28 micrograms/L; P less than 0.05). Eight weeks after stopping T,
while continuing GnRH alone, serum LH and FSH levels were similar to those
at the end of the first period of GnRH administration. The mean LH
response to GnRH was reduced during T administration (17 +/- 3
micrograms/L) compared to that during the initial period of GnRH alone (31
+/- 4 micrograms/L; P less than 0.05). Serum T and estradiol levels were
in the low normal range after GnRH alone before T administration (11 +/- 2
nmol/L and 105 +/- 17 pmol/L, respectively) and increased to just above
the normal adult ranges after 8 weeks of T administration (36 +/- 5 nmol/L
and 264 +/- 49 pmol/L, respectively). These results demonstrate that T
and/or its metabolites inhibit LH and FSH secretion by a GnRH-independent
mechanism, probably directly on the pituitary gland, in man.
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Citation
J Clin Endocrinol Metab. 1989 Feb;68(2):397-401
