Huber J, Reiterer E E, Sudi K, Gallistl S, Friedl K, Weinhandl G, Aigner R, Borkenstein M H
Department of Paediatrics, Division of Endocrinology and Diabetes, Medical University Graz, Austria.
Clin Endocrinol (Oxf). 2007 Jan;66(1):143-7. doi: 10.1111/j.1365-2265.2006.02701.x.
Ghrelin activates the growth hormone secretagogue receptor GHS-R. It strongly stimulates GH secretion and has a role in energy homeostasis. The relationship between plasma ghrelin and cortisol levels during insulin-induced hypoglycaemia in prepubertal and pubertal children has not yet been investigated. The aim of the present study was to establish whether insulin-induced hypoglycaemia stimulates ghrelin secretion and whether changes in ghrelin concentrations are related to changes in GH and cortisol in children.
We studied a group of 20 children and adolescents (five girls, 15 boys, mean age 10.8 +/- 3.7 years) undergoing insulin tolerance tests (ITTs) for clinical investigation of GH deficiency.
Stimulation tests were performed to investigate the relationship between ghrelin, GH, cortisol and glucose levels according to age and pubertal stage by determining the ghrelin profiles during insulin-induced hypoglycaemia (at 0, 60 and 120 min).
Ghrelin was significantly and inversely related to body weight, height, body mass index (BMI) and age of children (P < 0.05). Significant changes in ghrelin levels (P = 0.00013) were found after the insulin bolus, with a decline at 60 min and an increase to baseline values at 120 min. Changes in cortisol levels were negatively correlated with changes in ghrelin at 60 min (r = -0.59, P = 0.004) and at 120 min (r = -0.605, P = 0.003).
This study shows that ghrelin might not regulate the GH response to insulin-induced hypoglycaemia in prepubertal and pubertal children. A role for ghrelin in the regulation of cortisol secretion can be hypothesized concerning the negative correlation between changes in ghrelin and cortisol. Furthermore, the results imply that ghrelin secretion is age dependent and is a function of growth.
胃饥饿素可激活生长激素促分泌素受体GHS-R。它能强烈刺激生长激素分泌,并在能量平衡中发挥作用。青春期前和青春期儿童在胰岛素诱导的低血糖期间血浆胃饥饿素与皮质醇水平之间的关系尚未得到研究。本研究的目的是确定胰岛素诱导的低血糖是否会刺激胃饥饿素分泌,以及胃饥饿素浓度的变化是否与儿童生长激素和皮质醇的变化相关。
我们研究了一组20名儿童和青少年(5名女孩,15名男孩,平均年龄10.8±3.7岁),他们正在接受胰岛素耐量试验(ITT)以进行生长激素缺乏的临床研究。
通过测定胰岛素诱导的低血糖期间(0、60和120分钟)的胃饥饿素谱,根据年龄和青春期阶段进行刺激试验,以研究胃饥饿素、生长激素、皮质醇和葡萄糖水平之间的关系。
胃饥饿素与儿童的体重、身高、体重指数(BMI)和年龄显著负相关(P<0.05)。注射胰岛素后胃饥饿素水平有显著变化(P = 0.00013),60分钟时下降,120分钟时升至基线值。皮质醇水平的变化在60分钟时(r = -0.59,P = 0.004)和120分钟时(r = -0.605,P = 0.003)与胃饥饿素的变化呈负相关。
本研究表明,胃饥饿素可能无法调节青春期前和青春期儿童对胰岛素诱导的低血糖的生长激素反应。考虑到胃饥饿素和皮质醇变化之间的负相关,可以推测胃饥饿素在皮质醇分泌调节中发挥作用。此外,结果表明胃饥饿素分泌与年龄有关,是生长的一个函数。