Tuch B E, Osgerby K J, Turtle J R
Department of Medicine, University of Sydney, New South Wales, Australia.
Biochem Biophys Res Commun. 1988 Mar 30;151(3):1269-76.
Acute exposure to agents that activate protein kinase C is known to cause insulin release both from the fetal and adult pancreas. These experiments were designed to test the effect of chronic exposure of the human fetal pancreas to such agents. Nine to twelve days after commencement of culture of this tissue, exposed to 0.165-1.3 microM 12-O-tetradecanoylphorbol-13-acetate, insulin secretion was reduced and remained less than that for controls thereafter. Exchange of the test for the control medium resulted in partial recovery of insulin release. Insulin content of the treated explants was also significantly reduced. The insulinogenic response to an acute challenge of either 20 mM glucose or 10 mM theophylline/2.8 mM glucose at the end of the culture was no different from that for controls.
已知急性暴露于激活蛋白激酶C的物质会导致胎儿和成年胰腺释放胰岛素。这些实验旨在测试人类胎儿胰腺长期暴露于此类物质的影响。在该组织培养开始9至12天后,将其暴露于0.165 - 1.3微摩尔的12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯中,胰岛素分泌减少,此后一直低于对照组。将测试培养基换成对照培养基后,胰岛素释放部分恢复。经处理的外植体的胰岛素含量也显著降低。在培养结束时,对20毫摩尔葡萄糖或10毫摩尔茶碱/2.8毫摩尔葡萄糖的急性刺激的胰岛素生成反应与对照组无异。