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忧郁症期间垂体功能异常:α-黑素细胞刺激素分泌减少,促肾上腺皮质激素原非抑制性增加。

Abnormal pituitary function during melancholia: reduced alpha-melanocyte-stimulating hormone secretion and increased intact ACTH non-suppression.

作者信息

Maes M, DeJonckheere C, Vandervorst C, Schotte C, Cosyns P, Raus J, Suy E

机构信息

Department of Psychiatry, University Hospital of Antwerp, Belgium.

出版信息

J Affect Disord. 1991 Jul;22(3):149-57. doi: 10.1016/0165-0327(91)90048-w.

Abstract

In order to investigate pituitary alpha-melanocyte-stimulating hormone (alpha-MSH), intact (1-39 structure) adrenocorticotropic hormone (ACTH), and adrenal cortisol secretion, we measured 8 a.m. plasma levels of those hormones before and after administration of 1 mg dexamethasone in 39 depressed inpatients and 10 healthy controls. We found a significantly lower baseline alpha-MSH secretion in melancholic patients as opposed to healthy controls. There were no significant relations between alpha-MSH secretion on the one hand and ACTH or cortisol secretion on the other. Dexamethasone did not affect the 8 a.m. alpha-MSH circulating levels. The post-dexamethasone intact ACTH and cortisol values were significantly higher in melancholics as compared with healthy, minor and simple major depressed subjects. ACTH non-suppression was defined as post-dexamethasone intact ACTH greater than or equal to 12 pg/ml. ACTH non-suppression was found to be more sensitive (70%) and specific (100%) for melancholia than cortisol non-suppression. By means of pathway analysis we have established that cortisol non-suppression during a severe depression is completely determined by an augmented ACTH escape from suppression by dexamethasone. It is concluded that the assay of post-dexamethasone intact ACTH could, in the future, replace post-dexamethasone cortisol determination.

摘要

为了研究垂体α-黑素细胞刺激素(α-MSH)、完整的(1-39结构)促肾上腺皮质激素(ACTH)和肾上腺皮质醇的分泌情况,我们测定了39例抑郁住院患者和10名健康对照者在上午8点服用1毫克地塞米松前后这些激素的血浆水平。我们发现,与健康对照者相比,忧郁症患者的基线α-MSH分泌显著降低。一方面,α-MSH分泌与另一方面的ACTH或皮质醇分泌之间没有显著关系。地塞米松不影响上午8点时α-MSH的循环水平。与健康、轻度和单纯重度抑郁受试者相比,忧郁症患者服用地塞米松后的完整ACTH和皮质醇值显著更高。ACTH不被抑制的定义为服用地塞米松后完整ACTH大于或等于12皮克/毫升。结果发现,ACTH不被抑制对忧郁症的敏感性(70%)和特异性(100%)高于皮质醇不被抑制。通过路径分析我们确定,重度抑郁期间皮质醇不被抑制完全由地塞米松抑制ACTH的逃逸增加所决定。结论是,未来服用地塞米松后完整ACTH的检测可能会取代服用地塞米松后皮质醇的测定。

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