Benker G, Hackenberg K, Hamburger B, Reinwein D
Clin Endocrinol (Oxf). 1976 Mar;5(2):187-90. doi: 10.1111/j.1365-2265.1976.tb02831.x.
Growth hormone release-inhibiting hormone (GHR-IH) was administered to five patients with abnormal pituitary-adrenal function. There was immediate suppression by about 50% of ACTH levels in two patients who had undergone bilateral adrenalectomy because of Cushing's disease; one of them had Nelson's syndrome. Bromocryptine (2-5 mg) suppressed ACTH levels by 62-67% for more than 6 h in these patients. GHR-IH did not significantly influence cortisol secretion by an adrenal carcinoma and only slight changes were seen in two patients with Addison's disease. The possible therapeutic implications are discussed.
向五名垂体 - 肾上腺功能异常的患者注射了生长抑素释放抑制激素(GHR - IH)。两名因库欣病接受双侧肾上腺切除术的患者,促肾上腺皮质激素(ACTH)水平立即被抑制了约50%;其中一人患有尼尔森综合征。在这些患者中,溴隐亭(2 - 5毫克)使ACTH水平在6小时以上的时间内降低了62 - 67%。GHR - IH对肾上腺皮质癌的皮质醇分泌没有显著影响,在两名艾迪生病患者中仅观察到轻微变化。文中讨论了其可能的治疗意义。