Carnes M, Brownfield M, Lent S J, Nichols K, Schuler L
William S. Middleton Memorial Veterans Hospital, Madison, WI 53705.
Neuroendocrinology. 1992 Jan;55(1):97-104. doi: 10.1159/000126102.
Insulin-induced hypoglycemia is a metabolic stress that stimulates secretion of adrenocorticotropic hormone (ACTH) and cortisol in a number of animal species. Dexamethasone is a potent synthetic glucocorticoid that suppresses the secretion of ACTH and cortisol. Both ACTH and cortisol exhibit complex secretory patterns demonstrating ultradian and circadian rhythms. This work investigated the pattern of ACTH and cortisol response to hypoglycemia in goats and the effect of dexamethasone on this response. Five goats were pretreated with dexamethasone (0.1 mg/kg) and 5 with saline. Blood samples were taken every 2 min for 60 min before and 60 min after administration of insulin (2.5 IU/kg, i.v.). Immunoreactive ACTH and cortisol were measured in all samples and glucose in selected samples. Data sets were analyzed for significant pulses with the Cluster Analysis program. Complete data sets were compared as well as those for each 30-min interval. Plasma glucose was lower than preinsulin levels at 10 min, declined rapidly between 10 and 30 min, and remained low 30-60 min after insulin injection in both treatment groups. Controls showed a rapid rise in ACTH and cortisol beginning 30 +/- 10 min postinsulin. The increase in mean plasma hormone levels during hypoglycemia was predominantly due to an increase in amplitude of secretory pulses for ACTH and cortisol compared with the 30 min before insulin. Dexamethasone significantly lowered mean ACTH and cortisol levels and prevented alteration in plasma ACTH and cortisol secretion during hypoglycemia but did not totally ablate pulsatile activity of either hormone. The amplitude of ACTH and cortisol pulses was significantly decreased by dexamethasone treatment. The frequency of cortisol but not ACTH pulses was also significantly decreased.(ABSTRACT TRUNCATED AT 250 WORDS)
胰岛素诱导的低血糖是一种代谢应激,可刺激多种动物物种分泌促肾上腺皮质激素(ACTH)和皮质醇。地塞米松是一种强效合成糖皮质激素,可抑制ACTH和皮质醇的分泌。ACTH和皮质醇均表现出复杂的分泌模式,呈现出超日节律和昼夜节律。本研究调查了山羊对低血糖时ACTH和皮质醇的反应模式以及地塞米松对该反应的影响。5只山羊用地塞米松(0.1mg/kg)预处理,5只用生理盐水预处理。在静脉注射胰岛素(2.5IU/kg)前60分钟和后60分钟,每2分钟采集一次血样。检测所有样本中的免疫反应性ACTH和皮质醇,并检测选定样本中的葡萄糖。使用聚类分析程序分析数据集以确定显著脉冲。比较了完整数据集以及每个30分钟间隔的数据集。在两个治疗组中,血浆葡萄糖在10分钟时低于胰岛素注射前水平,在10至30分钟之间迅速下降,并在胰岛素注射后30至60分钟保持低水平。对照组在胰岛素注射后30±10分钟开始ACTH和皮质醇迅速升高。与胰岛素注射前30分钟相比,低血糖期间血浆激素平均水平的升高主要是由于ACTH和皮质醇分泌脉冲幅度的增加。地塞米松显著降低了ACTH和皮质醇的平均水平,并防止了低血糖期间血浆ACTH和皮质醇分泌的改变,但并未完全消除任何一种激素的脉冲活动。地塞米松治疗显著降低了ACTH和皮质醇脉冲的幅度。皮质醇脉冲频率显著降低,但ACTH脉冲频率未显著降低。(摘要截短至250字)