Boscaro M, Sonino N, Paoletta A, Rampazzo A, Mantero F
Institute of Semeiotica Medica, University of Padua, Italy.
J Clin Endocrinol Metab. 1988 Feb;66(2):255-7. doi: 10.1210/jcem-66-2-255.
The existence of feedback inhibition of ACTH on its own secretion has been postulated. To investigate its existence in man, the effects of synthetic ACTH 1-24 on endogenous ACTH secretion were tested in 13 patients with Addison's disease. Plasma ACTH was measured using an immunoradiometric assay, specific for endogenous ACTH 1-39. Ten patients were given 50 micrograms ACTH 1-24 as a bolus iv dose followed by a 50-microgram infusion in 90 min. Blood samples for ACTH and cortisol assay were obtained at 0, 15, 30, 60, 90, and 120 min. As a control, a saline infusion was given 2 days earlier. Three other patients were given 100 micrograms ovine corticotropin-releasing hormone (oCRH) iv and ACTH 1-24 as described above. Blood samples for ACTH and cortisol assay were drawn every 15 min for 2 hours. A CRH test was performed during saline infusion as a control 2 days earlier. In all patients steroid replacement therapy was maintained during the studies. ACTH 1-24 caused a significant decrease (P less than 0.01) in endogenous plasma ACTH at 15 min compared to saline. oCHR administration markedly stimulated ACTH release in the three patients tested, and the ACTH response to oCRH was completely inhibited by the simultaneous administration of ACTH 1-24. These findings strongly support the presence of ACTH autoregulation in man. The complete inhibition of the ACTH response to oCRH by exogenous ACTH 1-24 provides evidence for ultra-short feed-back inhibition at the pituitary level.
有人曾推测促肾上腺皮质激素(ACTH)对其自身分泌存在反馈抑制作用。为研究其在人体中的存在情况,对13例艾迪生病患者进行了合成ACTH 1 - 24对内源性ACTH分泌影响的测试。采用针对内源性ACTH 1 - 39的免疫放射分析法测定血浆ACTH。10例患者静脉推注50微克ACTH 1 - 24,随后在90分钟内输注50微克。在0、15、30、60、90和120分钟采集血样检测ACTH和皮质醇。作为对照,2天前给予生理盐水输注。另外3例患者静脉注射100微克羊促肾上腺皮质激素释放激素(oCRH)并按上述方法给予ACTH 1 - 24。在2小时内每15分钟采集血样检测ACTH和皮质醇。2天前在生理盐水输注期间进行CRH试验作为对照。在研究期间所有患者均维持类固醇替代治疗。与生理盐水相比,ACTH 1 - 24在15分钟时导致内源性血浆ACTH显著下降(P<0.01)。在3例受试患者中,oCHR给药显著刺激了ACTH释放,而同时给予ACTH 1 - 24可完全抑制ACTH对oCRH的反应。这些发现有力地支持了人体中存在ACTH自身调节。外源性ACTH 1 - 24对ACTH对oCRH反应的完全抑制为垂体水平的超短反馈抑制提供了证据。