Persson C G, Andersson K E, Kjellin G
Life Sci. 1986 Mar 24;38(12):1057-72. doi: 10.1016/0024-3205(86)90241-9.
It is well established that at low and clinically relevant concentrations theophylline (and caffeine) exerts antagonism at cell surface receptor sites for adenosine. However, it is not known which actions of theophylline are due to adenosine antagonism, because theophylline apparently activates other cellular mechanisms at the same low concentrations. Investigations into the actions of xanthines and their structure activity relationships have identified xanthine compounds like enprofylline (3-propylxanthine) that only has some actions in common with theophylline and that has a negligible ability to antagonize adenosine. Enprofylline is a more potent smooth muscle relaxant and antiasthmatic drug than theophylline but does not produce, e.g., theophylline-like diuretic effects, CNS-stimulant behavioural effects (restlessness - seizures), gastric secretory effects and release of free fatty acids. It is proposed that pharmacodynamic dissimilarities between enprofylline and theophylline may indicate physiological roles of adenosine.
众所周知,在低浓度且具有临床相关性的情况下,茶碱(和咖啡因)可在细胞表面的腺苷受体位点产生拮抗作用。然而,尚不清楚茶碱的哪些作用是由腺苷拮抗引起的,因为茶碱在相同的低浓度下显然还会激活其他细胞机制。对黄嘌呤及其构效关系的研究已鉴定出如恩丙茶碱(3 - 丙基黄嘌呤)这样的黄嘌呤化合物,它仅具有一些与茶碱相同的作用,且拮抗腺苷的能力可忽略不计。恩丙茶碱是一种比茶碱更强效的平滑肌松弛剂和抗哮喘药物,但不会产生例如茶碱样的利尿作用、中枢神经系统刺激行为效应(烦躁不安 - 惊厥)、胃分泌效应以及游离脂肪酸的释放。有人提出,恩丙茶碱和茶碱之间的药效学差异可能表明了腺苷的生理作用。