Ammon H P, Müller A B
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jul;326(4):364-7. doi: 10.1007/BF00501444.
The in vivo effect of forskolin on insulin release, blood glucose and intravenous glucose tolerance test has been studied in the rat. In addition in vitro experiments on the effect of forskolin on islet cAMP and insulin release have been performed for comparison purposes. In batch incubated islets forskolin increased cAMP levels concentration dependently, the EC50 being approximately 25 microM. The maximal effect occurred after 5 min. In the presence of 2.8 mM glucose 10 microM forskolin did not stimulate insulin release; however, it potentiated both phase of 11.1 mM glucose induced insulin secretion. I.v. administration of 1.5 mg/kg of forskolin increased blood glucose levels in rats, which was associated with significant elevation of serum insulin. During an i.v. glucose tolerance test forskolin potentiated the insulin releasing capacity of glucose but did not significantly affect blood glucose levels. It is conceivable that cAMP per se does not initiate but rather amplifies insulin release by glucose. Since the synergistic effect of forskolin and glucose on insulin release in vivo is not associated with increased elimination rate it is possible that forskolin exhibits additional effects which counteract the glucose lowering action of insulin.
已在大鼠中研究了福斯高林对胰岛素释放、血糖及静脉葡萄糖耐量试验的体内作用。此外,为作比较,还进行了福斯高林对胰岛环磷酸腺苷(cAMP)及胰岛素释放影响的体外实验。在批量孵育的胰岛中,福斯高林浓度依赖性地增加cAMP水平,半数有效浓度(EC50)约为25微摩尔。最大效应在5分钟后出现。在2.8毫摩尔葡萄糖存在的情况下,10微摩尔福斯高林不刺激胰岛素释放;然而,它增强了11.1毫摩尔葡萄糖诱导的胰岛素分泌的两个阶段。静脉注射1.5毫克/千克福斯高林可使大鼠血糖水平升高,这与血清胰岛素的显著升高有关。在静脉葡萄糖耐量试验期间,福斯高林增强了葡萄糖的胰岛素释放能力,但对血糖水平无显著影响。可以想象,cAMP本身并不启动而是放大葡萄糖诱导的胰岛素释放。由于福斯高林与葡萄糖在体内对胰岛素释放的协同作用与消除率增加无关,因此福斯高林可能具有抵消胰岛素降血糖作用的其他作用。