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糖皮质激素对不同垂体肿瘤患者生长激素分泌的调节作用。

Modulation by glucocorticoids of growth hormone secretion in patients with different pituitary tumors.

作者信息

Popovic V, Damjanovic S, Micic D, Manojlovic D, Micic J, Casanueva F F

机构信息

Institute of Endocrinology, University Clinical Center, Belgrade, Serbia.

出版信息

Neuroendocrinology. 1993 Oct;58(4):465-72. doi: 10.1159/000126577.

Abstract

The acute administration of glucocorticoids is a new stimulus of growth hormone (GH) secretion in man. In order to ascertain its point of action, and also the suitability of this new test as a diagnostic tool in GH pathological states, 33 subjects were studied. Eight of them were normal controls, and 25 were patients with tumors affecting the hypothalamopituitary area. A glucocorticoid stimulus, dexamethasone 4 mg i.v. was administered at 0 min and GH levels (means +/- SEM, microgram/l) were measured during the following 5 h. In addition, GH-releasing hormone (GHRH) and clonidine were employed as either pituitary or hypothalamic GH stimuli. Dexamethasone administration to normal subjects did not alter GH levels in the first 2 h of the test. Afterwards, a GH peak was observed around the third hour, GH levels returning to basal ones thereafter. The dexamethasone-induced GH peak (6.7 +/- 1.5) and area under the curve (526 +/- 137) were lower than after GHRH (14.0 +/- 4.5 and 1,070 +/- 369, respectively). In the 14 acromegalic patients studied, the GHRH-induced GH net increase was similar to that observed in controls, while the placebo did not alter GH basal levels. An absence of hypothalamic control was evident because clonidine did not stimulate GH release. On the other hand, and contrary to normal subjects, dexamethasone strongly inhibited GH secretion, the values being significantly lower when calculated either as mean GH peak, or maximum GH increment (delta). The delta GH was -2.5 +/- 3.1 after placebo, +3.7 +/- 4.5 after clonidine, +17.0 +/- 3.3 after GHRH and -13.4 +/- 4.5 following dexamethasone administration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

急性给予糖皮质激素是人类生长激素(GH)分泌的一种新刺激因素。为了确定其作用点,以及这种新测试作为GH病理状态诊断工具的适用性,对33名受试者进行了研究。其中8名是正常对照,25名是患有影响下丘脑 - 垂体区域肿瘤的患者。在0分钟时静脉注射4毫克地塞米松进行糖皮质激素刺激,并在接下来的5小时内测量GH水平(平均值±标准误,微克/升)。此外,使用生长激素释放激素(GHRH)和可乐定作为垂体或下丘脑的GH刺激物。对正常受试者给予地塞米松在测试的前2小时内未改变GH水平。此后,在大约第3小时观察到GH峰值,此后GH水平恢复到基础水平。地塞米松诱导的GH峰值(6.7±1.5)和曲线下面积(526±137)低于GHRH后的峰值(分别为14.0±4.5和1070±369)。在研究的14名肢端肥大症患者中,GHRH诱导的GH净增加与对照组观察到的相似,而安慰剂未改变GH基础水平。下丘脑控制缺失明显,因为可乐定未刺激GH释放。另一方面,与正常受试者相反,地塞米松强烈抑制GH分泌,无论是以平均GH峰值还是最大GH增量(δ)计算,其值均显著较低。安慰剂后δGH为 -2.5±3.1,可乐定后为 +3.7±4.5,GHRH后为 +17.0±3.3,地塞米松给药后为 -13.4±4.5。(摘要截短至250字)

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