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内源性和外源性糖皮质激素可降低人体血浆中的胃饥饿素水平。

Endogenous and exogenous glucocorticoids decrease plasma ghrelin in humans.

作者信息

Otto B, Tschöp M, Heldwein W, Pfeiffer A F H, Diederich S

机构信息

Medical Department, University Hospital Innenstadt, Ziemssenstrasse 1, 80336 Munich, Germany.

出版信息

Eur J Endocrinol. 2004 Jul;151(1):113-7. doi: 10.1530/eje.0.1510113.

Abstract

OBJECTIVE

The orexigenic and adipogenic peptide hormone ghrelin is predominantly produced and secreted by the stomach and seems to transduce changes in food intake to specific neuronal circuits in the brain. The activity of ghrelin also includes stimulatory effects on the corticotropic system. However, little is known about the influence of glucocorticoids on ghrelin levels. We therefore studied human plasma ghrelin levels in the presence and absence of elevated glucocorticoid levels of either endogenous or exogenous origin.

METHODS

Plasma ghrelin levels were measured in five patients with chronic hypercortisolism (aged 29-58, median 46 years) due to Cushing's syndrome before and after successful surgery for the adenoma, and in eight healthy controls (aged 24-39, median 27.5 years) before and after 30 mg prednisolone (for 5 days) once a day in the morning (median body mass index (BMI) 22.7 kg/m(2)). Plasma ghrelin levels were measured with a commercially available radioimmunoassay.

RESULTS

In patients with Cushing's syndrome, plasma ghrelin levels were low (median 363.2 pg/ml, range 161.9-525.7 pg/ml) and significantly increased by 26.6% (P=0.04) after successful surgery, while BMI decreased (median 26.2-24.0 kg/m(2), P=0.04). A strong negative correlation (r=-0.9, P=0.04) between changes in BMI and plasma ghrelin was observed. In healthy controls, plasma ghrelin levels (median 288.7 pg/ml, range 119.6-827.8 pg/ml) were significantly suppressed by 18.3% (P=0.04) after prednisolone treatment.

CONCLUSIONS

We have shown for the first time that plasma ghrelin levels are decreased under endogenously or exogenously induced hypercortisolism, making ghrelin an unlikely candidate for causing the changes in energy balance or body composition characteristic of Cushing's disease. However, the reduced ghrelin secretion could reflect a compensation mechanism in reaction to the metabolic consequences of chronic hypercortisolism.

摘要

目的

食欲肽和脂肪生成肽激素胃饥饿素主要由胃产生和分泌,似乎能将食物摄入量的变化传递至大脑中的特定神经回路。胃饥饿素的活性还包括对促肾上腺皮质激素系统的刺激作用。然而,关于糖皮质激素对胃饥饿素水平的影响知之甚少。因此,我们研究了内源性或外源性糖皮质激素水平升高时和未升高时人体血浆胃饥饿素水平。

方法

对5例因库欣综合征导致慢性皮质醇增多症的患者(年龄29 - 58岁,中位数46岁)在腺瘤成功手术后前后进行血浆胃饥饿素水平测量,对8名健康对照者(年龄24 - 39岁,中位数27.5岁)在每天早晨服用30 mg泼尼松龙(共5天)前后进行血浆胃饥饿素水平测量(中位体重指数(BMI)22.7 kg/m²)。采用市售放射免疫分析法测量血浆胃饥饿素水平。

结果

在库欣综合征患者中,血浆胃饥饿素水平较低(中位数363.2 pg/ml,范围161.9 - 525.7 pg/ml),成功手术后显著升高26.6%(P = 0.04),而BMI下降(中位数26.2 - 24.0 kg/m²,P = 0.04)。观察到BMI变化与血浆胃饥饿素之间存在强烈的负相关(r = -0.9,P = 0.04)。在健康对照者中,泼尼松龙治疗后血浆胃饥饿素水平(中位数288.7 pg/ml,范围119.6 - 827.8 pg/ml)显著降低18.3%(P = 0.04)。

结论

我们首次表明,在内源性或外源性诱导的皮质醇增多症情况下,血浆胃饥饿素水平会降低,这使得胃饥饿素不太可能是导致库欣病能量平衡或身体成分变化的原因。然而,胃饥饿素分泌减少可能反映了对慢性皮质醇增多症代谢后果的一种补偿机制。

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