Summers S T, Canonico P L, MacLeod R M, Rogol A D, Cronin M J
Eur J Pharmacol. 1985 May 20;111(3):371-6. doi: 10.1016/0014-2999(85)90644-2.
Phorbol esters are tumor promotors that directly stimulate protein kinase C activity. We asked whether these agents affect basal or receptor initiated alterations in growth hormone (GH) and prolactin release. In 4 h incubations of anterior pituitary cells, phorbol esters enhanced basal and GH releasing factor (GRF)-induced GH release. Somatostatin reduced by 38% the 4-fold stimulation of GH release induced by phorbol ester. These tumor promoters also reversed the ability of bromocriptine, a dopamine agonist, to inhibit prolactin release, with no apparent effect on basal prolactin secretion. When these agents were applied for 24 h, an increase in the basal release of both GH and prolactin was apparent. These data lead us to suggest that an intact protein kinase C system may be necessary for the full expression of GRF-stimulated GH release and dopaminergic inhibition of prolactin release.
佛波酯是直接刺激蛋白激酶C活性的肿瘤促进剂。我们研究了这些药物是否会影响基础状态下或受体启动的生长激素(GH)和催乳素释放的改变。在前脑垂体细胞4小时的孵育中,佛波酯增强了基础状态下以及生长激素释放因子(GRF)诱导的GH释放。生长抑素使佛波酯诱导的GH释放的4倍刺激降低了38%。这些肿瘤促进剂还逆转了多巴胺激动剂溴隐亭抑制催乳素释放的能力,对基础催乳素分泌没有明显影响。当应用这些药物24小时时,GH和催乳素的基础释放均明显增加。这些数据使我们推测,完整的蛋白激酶C系统对于GRF刺激的GH释放和多巴胺能对催乳素释放的抑制的充分表达可能是必需的。