Law G J, Ray K P, Wallis M
FEBS Lett. 1984 Jan 23;166(1):189-93. doi: 10.1016/0014-5793(84)80070-8.
A synthetic form of human pancreatic growth hormone releasing factor (GRF-44-NH2) was shown to be a potent stimulator of growth hormone (GH) secretion and cellular cyclic AMP levels in cultured sheep pituitary cells. A small dose-dependent stimulation of prolactin secretion was also observed. Somatostatin (0.5 microM) completely blocked the maximal GRF (1 nM)-stimulated secretion without a significant effect on cyclic AMP levels. Dopamine (0.1 microM) inhibited the GRF-elevated GH secretion by 50% and lowered cyclic AMP levels by 30%. Dopamine (0.1 microM) inhibition of basal prolactin secretion was not affected by GRF (1 nM). The data support the hypothesis that cyclic AMP is involved in the action of GRF but suggest that somatostatin can inhibit GRF-induced secretion of GH independently of cyclic AMP.
一种人工合成形式的人胰腺生长激素释放因子(GRF - 44 - NH₂)在培养的绵羊垂体细胞中被证明是生长激素(GH)分泌和细胞环磷酸腺苷(cAMP)水平的有效刺激物。还观察到对催乳素分泌有小剂量依赖性刺激作用。生长抑素(0.5微摩尔)完全阻断了最大剂量GRF(1纳摩尔)刺激的分泌,而对环磷酸腺苷水平无显著影响。多巴胺(0.1微摩尔)使GRF升高的GH分泌抑制50%,并使环磷酸腺苷水平降低30%。多巴胺(0.1微摩尔)对基础催乳素分泌的抑制不受GRF(1纳摩尔)影响。这些数据支持环磷酸腺苷参与GRF作用的假说,但表明生长抑素可独立于环磷酸腺苷抑制GRF诱导的GH分泌。