Hanew K, Tanaka A, Utsumi A, Sugawara A, Abe K
The Second Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
J Clin Endocrinol Metab. 1996 May;81(5):1952-5. doi: 10.1210/jcem.81.5.8626863.
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 micrograms and 10 micrograms GHRH or simultaneous infusion of 5 micrograms GHRH (iv for 75 min). However, 200 micrograms GHRH-Ant (iv for 75 min) significantly inhibited GH release, which was induced by simultaneous infusion of 5 micrograms GHRH. Although 100 micrograms GHRH-Ant could not significantly inhibit L-dopa-induced GH release, 200 micrograms 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.
使用生长激素释放激素拮抗剂(GHRH-Ant)在7名正常受试者中研究了GHRH-Ant对生长激素释放激素(GHRH)(1-44)NH2的相对抑制效力以及左旋多巴或可乐定诱导的生长激素释放机制。100微克GHRH-Ant(静脉注射75分钟)未抑制血浆生长激素对100微克和10微克GHRH推注或5微克GHRH同时输注(静脉注射75分钟)的反应。然而,200微克GHRH-Ant(静脉注射75分钟)显著抑制了由5微克GHRH同时输注诱导的生长激素释放。虽然100微克GHRH-Ant不能显著抑制左旋多巴诱导的生长激素释放,但200微克GHRH-Ant几乎完全抑制了该反应。同样,相同剂量的GHRH-Ant显著抑制了可乐定的生长激素释放活性。得出结论,GHRH-Ant对GHRH(1-44)NH2的抑制效力相对较弱(摩尔比约为1/60),并且左旋多巴或可乐定诱导的生长激素释放似乎是由下丘脑GHRH的释放介导的。