Brønstad G O, Christoffersen T
Eur J Biochem. 1981 Jul;117(2):369-74. doi: 10.1111/j.1432-1033.1981.tb06347.x.
Several prostaglandins were found to inhibit hormone-induced cyclic AMP accumulation in suspensions of intact rat hepatocytes. Prostaglandin E1 in concentrations of 0.05--25 micrometers inhibited the cyclic AMP response to glucagon. Maximal inhibition was about 50%. The effect was rapid, being evident within 30 s. Prostaglandins E2, F1 alpha, F2 alpha, A1 and A2 also inhibited the glucagon effect on cyclic AMP in hepatocytes. In cells made highly responsive to adrenaline, by pretreatment of the animals with the carcinogen 2-acetylaminofluorene, and inhibitory effect of prostaglandin E1 was seen also on adrenaline-induced cyclic AMP accumulation. The mechanism of the inhibitory effect of prostaglandins on hormone-stimulated cyclic AMP accumulation was not clarified. Prostaglandin E1 did not inhibit glucagon binding to intact hepatocytes, and so far we have not been able to demonstrate any effect of the prostaglandins on the adenylate cyclase or phosphodiesterase in broken cell preparations. It is concluded that while several previous studies have shown that stimulatory effects of prostaglandins on cyclic AMP are only marginal or lacking in parenchymal liver cells the present data indicate that several prostaglandins exert strong inhibitory interference with hormone-induced cyclic AMP accumulation.
研究发现,几种前列腺素可抑制激素诱导的完整大鼠肝细胞悬液中环状AMP的积累。浓度为0.05-25微摩尔的前列腺素E1可抑制对胰高血糖素的环状AMP反应。最大抑制率约为50%。该效应迅速,在30秒内即可显现。前列腺素E2、F1α、F2α、A1和A2也可抑制胰高血糖素对肝细胞中环状AMP的作用。在用致癌物2-乙酰氨基芴对动物进行预处理后,使细胞对肾上腺素高度敏感,此时也可观察到前列腺素E1对肾上腺素诱导的环状AMP积累具有抑制作用。前列腺素对激素刺激的环状AMP积累的抑制作用机制尚不清楚。前列腺素E1不抑制胰高血糖素与完整肝细胞的结合,到目前为止,我们还未能证明前列腺素对破碎细胞制剂中的腺苷酸环化酶或磷酸二酯酶有任何作用。结论是,虽然先前的几项研究表明,前列腺素对环状AMP的刺激作用在肝实质细胞中仅为边缘性或缺乏,但目前的数据表明,几种前列腺素对激素诱导的环状AMP积累具有强烈的抑制干扰作用。