del Pozo E, Martin-Perez J, Stadelmann A, Girard J, Brownell J
J Clin Invest. 1980 Jun;65(6):1531-4. doi: 10.1172/JCI109820.
In order to study the mechanism of action of a Met-enkephalin (FK 33824) on the pituitary-adrenal axis eight normal male volunteers were subjected to an ACTH stimulation test. Lysine-vasopressing (LVP), 5 IU, was injected intramuscularly after pretreatment with 0.5 mg FK 33824 i.m. or a placebo. In six of the subjects the opiate was again administered preceding a single injection of 0.25 mg ACTH beta 1-24 i.m. Blood was collected at regular intervals and ACTH and cortisol concentrations analyzed in all samples. LVP induced significant plasma ACTH (P < 0.05) and cortisol (P < 0.001) increases. Pretreatment with FK 33824 completely antagonized the effect of LVP. Furthermore, the cortisol elevation after exogenous ACTH was not modified by previous administration of FK 33824. It is concluded that the Met-enkephalin derivative FK 33824 directly suppresses ACTH release from the pituitary without influencing adrenal synthesis of cortisol.
为研究甲硫氨酸脑啡肽(FK 33824)对垂体 - 肾上腺轴的作用机制,对8名正常男性志愿者进行了促肾上腺皮质激素(ACTH)刺激试验。在用0.5mg FK 33824肌肉注射预处理或给予安慰剂后,肌肉注射5国际单位赖氨酸加压素(LVP)。在6名受试者中,在单次肌肉注射0.25mg促肾上腺皮质激素β1 - 24之前再次给予阿片类药物。定期采集血液,分析所有样本中的促肾上腺皮质激素和皮质醇浓度。LVP可使血浆促肾上腺皮质激素(P < 0.05)和皮质醇(P < 0.001)显著升高。用FK 33824预处理可完全拮抗LVP的作用。此外,外源性促肾上腺皮质激素后的皮质醇升高不受先前给予FK 33824的影响。得出的结论是,甲硫氨酸脑啡肽衍生物FK 33824直接抑制垂体释放促肾上腺皮质激素,而不影响肾上腺皮质醇的合成。