糖皮质激素级联假说重新审视:性腺类固醇的作用

Depression Pub Date : 1995-01-01 DOI:10.1002/depr.3050030105
Elizabeth A. Young M.D.
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引用次数: 31

摘要

HPA轴调节的性别差异在其他物种中也有记载,特别是在大鼠中,雌性激素调节皮质类固醇结合球蛋白(CBG)。鉴于抑郁症在女性中更为常见,性腺类固醇可能会影响抑郁症中常见的下丘脑轴失调。我们的一些研究比较了抑郁症男性和女性的下丘脑轴失调,表明存在差异。我们认为性腺激素可能在绝经前抑郁妇女中起调节作用。特别是,雌激素增加CBG水平,为高皮质醇血症提供更大的缓冲能力。此外,黄体酮可以作为糖皮质激素拮抗剂,从而阻断高皮质血症的一些负面后遗症。绝经后,对地塞米松抑制的抵抗率几乎增加到100%,这表明性腺类固醇的丧失是年龄- hpa轴相互作用的一个重要方面。抑郁症3:20-27(1995)。©1995 Wiley-Liss, Inc
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucocorticoid cascade hypothesis revisited: Role of gonadal steroids

Sex differences in HPA axis regulation have been documented in other species, particularly in rats, where estrogen regulates cortisosteroid binding globulin (CBG). Given that depression is more common in women, gonadal steroids may impact upon the HPA axis dysregulation often seen in depression. A number of our studies comparing HPA axis dysregulation in depressed men and women suggest that there are differences. We suggest that gonadal steroids may play a modulatory role in premenopansal depressed women. In particular, estrogen increases the level of CBG providing a greater buffering capacity against hypercortisolemia. In addition, progesterone can function as a glucocorticoid antagonist, thus blocking some of the negative sequellae of hypercortisolemia. Following menopause, the incidence of resistance to dexamethasone suppression increases to almost 100%, suggesting that loss of gonadal steroids is an important aspect of the age-HPA axis interaction. Depression 3:20–27 (1995). © 1995 Wiley-Liss, Inc.

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