Ray K P, Wallis M
Biochemistry Laboratory, School of Biological Sciences, University of Sussex, Falmer, Brighton, U.K.
Mol Cell Endocrinol. 1988 Aug;58(2-3):243-52. doi: 10.1016/0303-7207(88)90160-8.
Growth hormone-releasing hormone (GHRH) and the phorbol ester tetradecanoylphorbol acetate (TPA) each stimulated a rapid and extensive (up to 15-fold) increase in the secretion of growth hormone from cultured ovine anterior pituitary cells. Effects of the releasing hormone on growth hormone secretion were associated with a concurrent, large increase in cellular cyclic AMP accumulation. TPA induced a much smaller (26-78%), though still significant, increase in cellular cyclic AMP levels. Forskolin and isobutylmethylxanthine (IBMX) also stimulated growth hormone secretion and cyclic AMP accumulation. When combined with a maximally effective concentration of GHRH these compounds did not further elevate growth hormone secretion even though they induced further increases in cyclic AMP concentration; this is consistent with activation occurring via a common cyclic AMP-dependent pathway. In contrast TPA when combined with maximally effective concentrations of either GHRH, forskolin or IBMX caused additional release of growth hormone, suggesting that the TPA-induced secretion involved a cyclic AMP-independent process. However, TPA also markedly potentiated the cellular cyclic AMP accumulation due to each of these agents. That TPA induced stimulation of basal and GHRH-stimulated cyclic AMP levels measured in the presence of IBMX suggests an action affecting cyclic AMP synthesis. Carbachol had no effect on basal or GHRH-stimulated growth hormone secretion or cyclic AMP levels. The two actions of TPA, one on secretion and one on cyclic AMP metabolism, may result from activation of some common event possibly involving protein kinase C. Our results suggest that GHRH and TPA activate independent pathways regulating growth hormone secretion.
生长激素释放激素(GHRH)和佛波酯十四酰佛波醇乙酸酯(TPA)均可刺激培养的绵羊垂体前叶细胞快速大量(高达15倍)地分泌生长激素。释放激素对生长激素分泌的影响与细胞内环磷酸腺苷(cAMP)积累同时大幅增加有关。TPA诱导细胞内cAMP水平的升高幅度要小得多(26% - 78%),尽管仍具有统计学意义。福斯高林和异丁基甲基黄嘌呤(IBMX)也能刺激生长激素分泌和cAMP积累。当与最大有效浓度的GHRH联合使用时,这些化合物即使能进一步提高cAMP浓度,也不会进一步提高生长激素分泌;这与通过共同的cAMP依赖性途径发生激活作用一致。相比之下,TPA与最大有效浓度的GHRH、福斯高林或IBMX联合使用时,会导致额外的生长激素释放,这表明TPA诱导的分泌涉及一个不依赖cAMP的过程。然而,TPA也显著增强了这些药物各自引起的细胞内cAMP积累。在存在IBMX的情况下测量到TPA诱导基础和GHRH刺激的cAMP水平升高,这表明其作用影响cAMP合成。卡巴胆碱对基础或GHRH刺激的生长激素分泌或cAMP水平没有影响。TPA的两种作用,一种对分泌的作用,一种对cAMP代谢的作用,可能是由一些可能涉及蛋白激酶C的共同事件激活所致。我们的结果表明,GHRH和TPA激活独立的途径来调节生长激素分泌。