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J. Biol. Chem., Vol. 255, Issue 2, 342-344, 01, 1980
Z Naor and KJ Catt
Gonadotropin releasing hormone (GnRH) and its potent analog [D-
Ser(tBu)6]des-Gly10-GnRH N-ethylamide elevate pituitary cyclic GMP levels
while stimulating gonadotropin release in cultured pituitary cells.
Addition of mycophenolic acid to pituitary cell cultures decreased basal
and GnRH-induced cGMP production to undetectable levels, but did not reduce
basal or GnRH-stimulated luteinizing hormone (LH) release. Elevation of
endogenous cGMP levels by sodium nitroprusside, or addition of cGMP or its
potent derivatives, was also without effect on basal or GnRH-stimulated LH
release. These findings demonstrate that the elevation of intracellular
cGMP during GnRH action does not mediate the release of LH by pituitary
cells.
Independent actions of gonadotropin releasing hormone upon cyclic GMP production and luteinizing hormone release
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