Perras Boris, Schultes Bernd, Schwaiger Rita, Metz Christian, Wesseler Wiebke, Born Jan, Fehm Horst Lorenz
Department of Neuroendocrinology, University of Lübeck, Lübeck, Germany.
Regul Pept. 2002 Dec 31;110(1):85-91. doi: 10.1016/s0167-0115(02)00163-5.
Early sleep in humans is characterized by a distinct suppression of pituitary-adrenal activity coinciding with enhanced activity of the somatotropic axis. Here, we tested in awake humans the hypothesis of an inhibiting influence of hypothalamic growth hormone-releasing hormone (GHRH) on pituitary-adrenal activity. For this purpose, pituitary-adrenal activity was stimulated in 10 men through a standard insulin-hypoglycemia-test (IHT) and in another 10 men through combined administration of CRH/vasopressin. Stimulation was performed in each man on three conditions following pretreatment with Placebo and GHRH administered intravenously (50 microg) or intranasally (300 microg) 1 h before. GH, ACTH and cortisol as well as blood pressure and heart rate were measured repeatedly. Contrary to expectations, pretreatment with GHRH did not suppress but enhanced secretion of cortisol upon insulin-induced hypoglycemia regardless of the route of GHRH pretreatment (p<0.05). In contrast, GHRH did not facilitate cortisol release after stimulation with CRH/vasopressin. Changes in ACTH remained inconsistent. Plasma levels of GH increased significantly after i.v. GHRH application, but remained unchanged after the intranasal administration. Blood pressure and heart rate were not influenced by the treatments. Results indicate facilitating effects of GHRH mediated at a suprapituitary (i.e. hypothalamic) level as suggested by restriction of the effect to the hypoglycemia-induced cortisol release with no effects after pituitary stimulation with CRH/vasopressin.
人类早期睡眠的特征是垂体 - 肾上腺活动明显受到抑制,同时生长激素轴的活动增强。在此,我们在清醒的人类中测试了下丘脑生长激素释放激素(GHRH)对垂体 - 肾上腺活动具有抑制作用的假说。为此,通过标准胰岛素低血糖试验(IHT)刺激10名男性的垂体 - 肾上腺活动,通过联合给予促肾上腺皮质激素释放激素(CRH)/血管加压素刺激另外10名男性的垂体 - 肾上腺活动。在每位男性中,在分别静脉注射(50微克)或鼻内给予(300微克)安慰剂和GHRH预处理1小时后的三种条件下进行刺激。重复测量生长激素(GH)、促肾上腺皮质激素(ACTH)和皮质醇以及血压和心率。与预期相反,无论GHRH预处理的途径如何,GHRH预处理均未抑制而是增强了胰岛素诱导的低血糖时皮质醇的分泌(p<0.05)。相反,GHRH在CRH/血管加压素刺激后并未促进皮质醇释放。ACTH的变化仍然不一致。静脉注射GHRH后血浆GH水平显著升高,但鼻内给药后保持不变。血压和心率不受治疗影响。结果表明,GHRH的促进作用是在垂体上(即下丘脑)水平介导的,这一点由其作用仅限于低血糖诱导的皮质醇释放而在CRH/血管加压素刺激垂体后无作用所表明。