Ghigo M C, Torsello A, Grilli R, Luoni M, Guidi M, Cella S G, Locatelli V, Müller E E
Dipartimento di Farmacologia, Università degli Studi di Milano, Italy.
J Endocrinol Invest. 1997 Mar;20(3):144-50. doi: 10.1007/BF03346893.
The individual role played by GH and IGF-I in the regulation of hypothalamic GHRH and SRIF gene expression is still object of debate. We have investigated the effect of exogenously administered recombinant hGH (rhGH) and recombinant hIGF-I (rhIGF-I) in ad libitum fed control and starved rats, the latter an animal model which is characterized by low circulating levels of endogenous GH and IGF-I. Adult male rats were fed ad libitum (C) or food-deprived (S) for 72 hours; rats in either C or S groups were treated with systemic administration of rhGH and rhIGF-I for 3 days. GHRH, SRIF and GH mRNA levels were evaluated by Northern and slot blot hybridization. Administration of rhGH (250 micrograms/kg/twice daily, sc) induced a significant inhibition of GHRH and a significant stimulation of SRIF mRNA levels in C rats; GH treatment was, however, ineffective on both neuropeptide mRNA levels in the S group. Continuous infusion of rhIGF-I (300 micrograms/kg/day, sc) induced a significant increase of SRIF levels in both C and S rats but did not modify GHRH mRNA levels in either group. In the pituitary, GH mRNA levels followed a pattern very similar to that of GHRH. These results provide evidence for a direct role of GH in the inhibition of GHRH mRNA levels; IGF-I appears more involved in the direct stimulation of SRIF mRNA levels.
生长激素(GH)和胰岛素样生长因子-I(IGF-I)在下丘脑生长激素释放激素(GHRH)和生长抑素(SRIF)基因表达调控中所起的个体作用仍是一个有争议的话题。我们研究了外源性给予重组人GH(rhGH)和重组人IGF-I(rhIGF-I)对随意进食的对照大鼠和饥饿大鼠的影响,后者是一种以内源性GH和IGF-I循环水平低为特征的动物模型。成年雄性大鼠随意进食(C组)或禁食(S组)72小时;C组和S组大鼠均接受rhGH和rhIGF-I全身给药3天。通过Northern和狭缝印迹杂交评估GHRH、SRIF和GH mRNA水平。给予rhGH(250微克/千克/每日两次,皮下注射)可显著抑制C组大鼠的GHRH并显著刺激SRIF mRNA水平;然而,GH治疗对S组的两种神经肽mRNA水平均无效。持续输注rhIGF-I(300微克/千克/天,皮下注射)可使C组和S组大鼠的SRIF水平均显著升高,但两组的GHRH mRNA水平均未改变。在垂体中,GH mRNA水平的变化模式与GHRH非常相似。这些结果为GH在抑制GHRH mRNA水平中起直接作用提供了证据;IGF-I似乎更多地参与直接刺激SRIF mRNA水平。