TY - JOUR
T1 - The Inhibitory Effects of Growth Hormone-Releasing Hormone (GHRH)-Antagonist on GHRH, L-Dopa, and Clonidine-Induced GH Secretion in Normal Subjects
AU - Hanew, Kunihiko
AU - Tanaka, Aki
AU - Utsumi, Atsushi
AU - Sugawara, Akira
AU - Abe, Keishi
PY - 1996
Y1 - 1996
N2 - The relative inhibitory potency of GHRH-Antagonist (GHRH-Ant) to GHRH(1-44)NH2 and mechanism of L-dopa- or clonidine-induced GH release were studied in seven normal subjects using GHRH-Ant. One hundred micrograms of GHRH-Ant (iv for 75 min) did not inhibit plasma GH responses to bolus injection of 100 μg and 10 μg GHRH or simultaneous infusion of 5 μg GHRH (iv for 75 min). However, 200 μg GHRH-Ant (iv for 75 min) significantly inhibited GH release, which was induced by simultaneous infusion of 5 μg GHRH. Although 100 μg GHRH-Ant could not significantly inhibit L-dopa-induced GH release, 200 μg GHRH-Ant almost completely inhibited the response. Similarly, the same dose of GHRH-Ant markedly inhibited the GH-releasing activity of clonidine. It is concluded that the inhibitory potency of GHRH-Ant on GHRH(1-44)NH2 is relatively weak (about 1/60 in molar base), and that L-dopa- or clonidine-induced GH release seems to be mediated by the release of hypothalamic GHRH.
AB - The relative inhibitory potency of GHRH-Antagonist (GHRH-Ant) to GHRH(1-44)NH2 and mechanism of L-dopa- or clonidine-induced GH release were studied in seven normal subjects using GHRH-Ant. One hundred micrograms of GHRH-Ant (iv for 75 min) did not inhibit plasma GH responses to bolus injection of 100 μg and 10 μg GHRH or simultaneous infusion of 5 μg GHRH (iv for 75 min). However, 200 μg GHRH-Ant (iv for 75 min) significantly inhibited GH release, which was induced by simultaneous infusion of 5 μg GHRH. Although 100 μg GHRH-Ant could not significantly inhibit L-dopa-induced GH release, 200 μg GHRH-Ant almost completely inhibited the response. Similarly, the same dose of GHRH-Ant markedly inhibited the GH-releasing activity of clonidine. It is concluded that the inhibitory potency of GHRH-Ant on GHRH(1-44)NH2 is relatively weak (about 1/60 in molar base), and that L-dopa- or clonidine-induced GH release seems to be mediated by the release of hypothalamic GHRH.
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U2 - 10.1210/jcem.81.5.8626863
DO - 10.1210/jcem.81.5.8626863
M3 - Article
C2 - 8626863
AN - SCOPUS:0029933620
SN - 0021-972X
VL - 81
SP - 1952
EP - 1955
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 5
ER -