Gold P W, Calabrese J R, Kling M A, Avgerinos P, Khan I, Gallucci W T, Tomai T P, Chrousos G P
Prog Neuropsychopharmacol Biol Psychiatry. 1986;10(1):57-65. doi: 10.1016/0278-5846(86)90044-8.
To further explore hypothalamic pituitary adrenal regulation in patients with affective illness, we administered 1 microgram/kg of synthetic ovine corticotropin releasing factor at 2000h to 26 drug-free patients with this disorder and to 15 healthy controls. Compared to controls, depressed patients (N = 12) showed a significant elevation in baseline cortisol and significant reductions in the net ACTH and cortisol responses to corticotropin releasing factor. These findings were normal in manic (N = 6) and improved (N = 8) subjects. An additional finding was that baseline cortisol and net ACTH and cortisol responses to CRF were negatively correlated in the entire group of patients and controls as well as in the patients alone. These data indicate that the reduced ACTH and cortisol responses to CRF in depression reflect normal functioning of the pituitary corticotroph cell (i.e., that the negative feedback effect of cortisol on ACTH secretion in depression is physiologically intact, effectively serving as a brake on the ACTH response to exogenous CRF. Thus, the hypercortisolism of depression may be due to a hypothalamic defect, possibly involving hypersecretion of endogenous CRF. This possibility may be of particular interest in light of clinical observations that depression can often be precipitated by stress and by data in experimental animals that CRF may influence several processes known to be altered in the overall symptom complex of depression.
为了进一步探究情感性疾病患者下丘脑 - 垂体 - 肾上腺轴的调节情况,我们于20:00给26例未服用药物的情感性疾病患者及15名健康对照者静脉注射1微克/千克的合成羊促肾上腺皮质激素释放因子(CRF)。与对照组相比,抑郁症患者(n = 12)的基础皮质醇水平显著升高,对促肾上腺皮质激素释放因子的促肾上腺皮质激素(ACTH)和皮质醇净反应显著降低。这些结果在躁狂症患者(n = 6)和病情改善的患者(n = 8)中是正常的。另外一个发现是,在所有患者和对照组以及仅在患者组中,基础皮质醇水平以及对CRF的ACTH和皮质醇净反应均呈负相关。这些数据表明,抑郁症患者对CRF的ACTH和皮质醇反应降低反映了垂体促肾上腺皮质激素细胞的正常功能(即抑郁症中皮质醇对ACTH分泌的负反馈作用在生理上是完整的,有效地抑制了ACTH对外源性CRF的反应)。因此,抑郁症患者的高皮质醇血症可能是由于下丘脑缺陷,可能涉及内源性CRF分泌过多。鉴于临床观察到抑郁症常由应激诱发,以及实验动物数据表明CRF可能影响抑郁症整体症状复合体中已知发生改变的多个过程,这种可能性可能特别值得关注。