Canonico P L, Cronin M J, Thorner M O, MacLeod R M
Am J Physiol. 1983 Dec;245(6):E587-90. doi: 10.1152/ajpendo.1983.245.6.E587.
The effects of natural and synthetic human pancreatic growth hormone-releasing factor (hpGRF) on 32P incorporation into phospholipids were studied in cultured rat anterior pituitary cells. Natural hpGRF (1:30 dilution) significantly (P less than 0.01) stimulated phosphatidylinositol labeling at all times studied (15, 30, and 60 min). Synthetic hpGRF-(1-40)OH also significantly (P less than 0.05; P less than 0.01) increased 32P incorporation into phosphatidylinositol in a dose-related (1-30 nM) and time-dependent (5, 10, and 30 min) manner. In contrast, phosphatidylcholine and phosphatidylethanolamine labeling was not affected at any time studied. Somatostatin (30 nM) did not affect basal or hpGRF-stimulated phosphatidylinositol labeling but inhibited the hpGRF stimulation of cyclic AMP accumulation and growth hormone release. These results suggest that the phosphatidylinositol cycle may be involved in the mechanism of action of hpGRF in the anterior pituitary gland.
在培养的大鼠垂体前叶细胞中,研究了天然和合成的人胰腺生长激素释放因子(hpGRF)对磷脂中32P掺入的影响。天然hpGRF(1:30稀释)在所有研究时间(15、30和60分钟)均显著(P小于0.01)刺激磷脂酰肌醇标记。合成的hpGRF-(1-40)OH也显著(P小于0.05;P小于0.01)以剂量相关(1-30 nM)和时间依赖性(5、10和30分钟)的方式增加32P掺入磷脂酰肌醇。相反,在任何研究时间,磷脂酰胆碱和磷脂酰乙醇胺标记均未受影响。生长抑素(30 nM)不影响基础或hpGRF刺激的磷脂酰肌醇标记,但抑制hpGRF对环磷酸腺苷积累和生长激素释放的刺激。这些结果表明,磷脂酰肌醇循环可能参与hpGRF在垂体前叶的作用机制。