Díez J J, Iglesias P, Aguilera A, Bajo M A, Selgas R
Department of Endocrinology, Hospital La Paz, Madrid, Spain.
Nephrol Dial Transplant. 1999 Jul;14(7):1704-9. doi: 10.1093/ndt/14.7.1704.
Several alterations in growth hormone (GH) secretion have been reported in patients with chronic renal insufficiency. However, cholinergic modulation of somatotopic cell function has not been fully clarified in uraemic patients. To gain further insight into the disrupted mechanism of GH regulation in chronic renal failure, we investigated whether the blockade of cholinergic muscarinic receptor with pirenzepine could modify the response of GH to its physiological releasing hormone.
Eight uraemic male patients on peritoneal dialysis and six normal controls were studied. All subjects underwent two endocrine tests in random order. In one of them placebo was administered 60 min before the injection of GH-releasing hormone (GHRH, 100 microg, i.v. in bolus at 0 min). In another the muscarinic blocking agent pirenzepine, 100 mg p.o., was administered at that time. Blood samples for GH were collected at -60, 0, 15, 30, 45, 60 and 90 min.
Baseline plasma GH concentrations were similar in patients and controls. GH responses to GHRH were characterized by great interindividual variability in uraemic patients with regard to the amount and the time to maximal peak. In the placebo plus GHRH test, the maximum GH concentrations in patients (14.0 +/- 3.2 microg/l) were similar to those reached by controls (18.0 +/- 3.1 microg/l), although GH secretion was more sustained in patients. The area under the secretory curve (AUC) of GH secretion in patients was also similar to that found in controls (14.4 +/- 2.9 vs 15.4 +/- 3.3 microg/h/l). When subjects were given pirenzepine before GHRH injection an abolishment of GHRH-induced GH release was observed in all controls and in all but one of the uraemic patients. The AUC of GH secretion was, therefore, significantly reduced both in uraemic patients (4.1 +/- 2.0 microg/h/l, P<0.05) and in control subjects (2.0 +/- 0.3 microg/h/l, P<0.05).
These results suggest that GH secretion in uraemic patients is modulated, at least in part, by a cholinergic mechanism. The muscarinic blockade, possibly acting via an increase in somatostatin release, is able to inhibit GH release in response to direct pituitary stimulation with GHRH.
慢性肾功能不全患者中已报道生长激素(GH)分泌存在多种改变。然而,尿毒症患者中胆碱能对生长激素分泌细胞功能的调节尚未完全阐明。为了进一步深入了解慢性肾衰竭中GH调节的破坏机制,我们研究了用哌仑西平阻断胆碱能毒蕈碱受体是否能改变GH对其生理释放激素的反应。
研究了8名接受腹膜透析的尿毒症男性患者和6名正常对照者。所有受试者随机顺序接受两项内分泌测试。其中一项测试中,在注射生长激素释放激素(GHRH,100μg,静脉推注,0分钟时)前60分钟给予安慰剂。另一项测试中,此时口服100mg毒蕈碱阻断剂哌仑西平。在-60、0、15、30、45、60和90分钟采集血样检测GH。
患者和对照者的基线血浆GH浓度相似。在尿毒症患者中,GH对GHRH的反应在峰值量和达到最大峰值的时间方面存在很大的个体差异。在安慰剂加GHRH测试中,患者的最大GH浓度(14.0±3.2μg/L)与对照者达到的浓度(18.0±3.1μg/L)相似,尽管患者的GH分泌更持久。患者GH分泌的分泌曲线下面积(AUC)也与对照者相似(14.4±2.9对15.4±3.3μg/h/L)。当在GHRH注射前给受试者服用哌仑西平时,在所有对照者以及除一名尿毒症患者外的所有患者中均观察到GHRH诱导的GH释放被消除。因此,尿毒症患者(4.1±2.0μg/h/L,P<0.05)和对照者(2.0±0.3μg/h/L,P<0.05)的GH分泌AUC均显著降低。
这些结果表明,尿毒症患者的GH分泌至少部分受胆碱能机制调节。毒蕈碱阻断可能通过增加生长抑素释放起作用,能够抑制GH对GHRH直接垂体刺激的释放反应。