Wehrenberg W B, Baird A, Klepper R, Mormede P, Ling N
Department of Health Sciences, University of Wisconsin-Milwaukee 53201.
Regul Pept. 1989 Apr;25(1):147-55. doi: 10.1016/0167-0115(89)90256-5.
While chronic glucocorticoid treatment increases pituitary growth hormone (GH) content in rats and primates and increases pituitary GH release in response to growth hormone-releasing hormone (GHRH) in rats, it also inhibits somatic growth. We investigated these opposite actions in rats using the synthetic glucocorticoid dexamethasone. Seven days of dexamethasone treatment (40 micrograms/animal per day) did not alter the frequency of spontaneous GH pulses in conscious, freely-moving animals. The amplitude of the GH pulses in saline and dexamethasone-treated rats was different (P less than 0.01), the latter group having a higher incidence of GH levels less than 95 ng/ml, a lower incidence of GH levels between 96 and 251 ng/ml, and a higher incidence of GH values greater than 480 ng/ml. A 20 microgram/kg per day dose of dexamethasone was sufficient to significantly inhibit growth but was inadequate in enhancing the GH response to an acute injection of GHRH in anesthetized animals. These results support the concept that glucocorticoids exert their catabolic effects on somatic growth in peripheral tissues and not at the pituitary level.
虽然长期使用糖皮质激素治疗可增加大鼠和灵长类动物垂体生长激素(GH)的含量,并增强大鼠垂体对生长激素释放激素(GHRH)的反应性释放GH,但它也会抑制躯体生长。我们使用合成糖皮质激素地塞米松在大鼠中研究了这些相反的作用。地塞米松治疗7天(40微克/动物/天)并未改变清醒、自由活动动物中GH自发脉冲的频率。生理盐水处理组和地塞米松处理组大鼠的GH脉冲幅度不同(P<0.01),后一组中GH水平低于95纳克/毫升的发生率较高,GH水平在96至251纳克/毫升之间的发生率较低,而GH值大于480纳克/毫升的发生率较高。每天20微克/千克剂量的地塞米松足以显著抑制生长,但不足以增强麻醉动物对急性注射GHRH的GH反应。这些结果支持这样一种观点,即糖皮质激素对躯体生长的分解代谢作用是在外周组织而非垂体水平发挥的。