Besser G M, Mortimer C H, McNeilly A S, Thorner M O, Batistoni G A, Bloom S R, Kastrup K W, Hanssen K F, Hall R, Coy D H, Kastin A J, Schally A V
Br Med J. 1974 Dec 14;4(5945):622-7. doi: 10.1136/bmj.4.5945.622.
Growth hormone release inhibiting hormone (GH-RIH) was infused at a rate of 1.3 mug/min for 28 hours into four patients with acromegaly, two of whom also had clinical diabetes mellitus. Growth hormone and glucagon were suppressed throughout the infusion though delayed secretion of insulin occurred in association with both meals and an oral glucose load. Glucose tolerance was improved in one diabetic patient who was taking chlorpropamide while the other required much less insulin than usual. Secretion of endogenous thyroid-stimulating hormone was lowered in one euthyroid patient on carbimazole. Luteinizing hormone, follicle-stimulating hormone, ACTH, and prolactin were not affected. Serum somatomedin levels were reduced in one patient. There was a rapid rebound of all the suppressed hormones when the infusions stopped. Longer-acting analogues of GH-RIH will be needed before long-term therapy of acromegaly or diabetes mellitus becomes possible, but such preparations should be available soon for clinical trial.
以1.3微克/分钟的速率向4例肢端肥大症患者输注生长抑素释放抑制激素(GH-RIH),持续28小时,其中2例还患有临床糖尿病。在整个输注过程中,生长激素和胰高血糖素受到抑制,不过胰岛素分泌延迟与进餐及口服葡萄糖负荷均有关。1例服用氯磺丙脲的糖尿病患者的葡萄糖耐量得到改善,而另1例所需胰岛素量比平时少得多。1例服用卡比马唑的甲状腺功能正常患者的内源性促甲状腺激素分泌降低。促黄体生成素、促卵泡激素、促肾上腺皮质激素和催乳素未受影响。1例患者的血清生长调节素水平降低。输注停止后,所有受抑制的激素均迅速出现反弹。在肢端肥大症或糖尿病的长期治疗成为可能之前,不久将需要作用时间更长的GH-RIH类似物,但此类制剂应很快可用于临床试验。