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在人体缺乏糖皮质激素反馈的情况下持续给予人促肾上腺皮质激素释放激素。

Continuous administration of human corticotropin-releasing hormone in the absence of glucocorticoid feedback in man.

作者信息

Ur E, Capstick C, McLoughlin L, Checkley S, Besser G M, Grossman A

机构信息

Division of Endocrinology, Memorial University, St. John's, Nfld., Canada.

出版信息

Neuroendocrinology. 1995 Feb;61(2):191-7. doi: 10.1159/000126840.

Abstract

Continuous 24-hour infusions of a maximally stimulating dose (1 microgram/kg/h) of corticotropin-releasing hormone (CRH) have been shown to cause elevations of plasma cortisol and ACTH, but the pattern of results were confounded by serum cortisol causing feedback changes. We have looked at ACTH responses to saline or CRH infusions over 24 h in 6 normal subjects who, in addition, received either placebo or metyrapone, an 11 beta-hydroxylase inhibitor which blocks the formation of cortisol and thus abolishes glucocorticoid feedback. Cortisol and ACTH levels were measured by radioimmunoassay. Before metyrapone, CRH infusion resulted in exaggerated ACTH peaks throughout the day, as compared with normal saline: there was no influence on the noctural rise in ACTH. Following metyrapone alone, absolute cortisol levels were lower but circadian rhythmicity was preserved. Circadian rhythm of ACTH was maintained, with a fall in the evening to 14.5 +/- 4 pg/ml (mean +/- SE) at midnight and an exaggerated rise overnight, reaching a peak level of 90 +/- 33 pg/ml at 07:00 h. Subjects receiving CRH with metyrapone showed a similar pattern of responses, but with further enhanced ACTH levels. The evening fall reached a nadir of 30 +/- 6 pg/ml at 01:00 h. With diminished glucocorticoid feedback the nocturnal rise in ACTH was augmented by CRH infusion, with a morning peak of 193 +/- 21 pg/ml at 07:00 h. Thus, continuous infusion of CRH in the absence of steroid feedback leads to a retention of the circadian rhythmicity in ACTH secretion, reset at a higher absolute level.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

持续24小时输注最大刺激剂量(1微克/千克/小时)的促肾上腺皮质激素释放激素(CRH)已被证明可导致血浆皮质醇和促肾上腺皮质激素(ACTH)升高,但结果模式因血清皮质醇引起的反馈变化而混淆。我们观察了6名正常受试者在24小时内对生理盐水或CRH输注的ACTH反应,此外,这些受试者还接受了安慰剂或甲吡酮,甲吡酮是一种11β-羟化酶抑制剂,可阻断皮质醇的形成,从而消除糖皮质激素反馈。通过放射免疫测定法测量皮质醇和ACTH水平。在使用甲吡酮之前,与生理盐水相比,CRH输注导致全天ACTH峰值夸大:对ACTH夜间升高没有影响。单独使用甲吡酮后,绝对皮质醇水平较低,但昼夜节律得以保留。ACTH的昼夜节律得以维持,午夜时降至14.5±4皮克/毫升(平均值±标准误),夜间升高夸大,在07:00时达到峰值水平90±33皮克/毫升。接受CRH和甲吡酮的受试者表现出类似的反应模式,但ACTH水平进一步升高。夜间下降在01:00时达到最低点30±6皮克/毫升。随着糖皮质激素反馈减弱,CRH输注增强了ACTH的夜间升高,07:00时早晨峰值为193±21皮克/毫升。因此,在没有类固醇反馈的情况下持续输注CRH会导致ACTH分泌的昼夜节律得以保留,并在更高的绝对水平上重新设定。(摘要截断于250字)

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