Boulenger J P, Patel J, Marangos P J
Neurosci Lett. 1982 May 28;30(2):161-6. doi: 10.1016/0304-3940(82)90290-7.
The binding of various adenosine receptor ligands and of [3H]diazepam, as well as their inhibition of methylxanthines, have been studied in human brain cerebral cortex membranes. Caffeine and theophylline competitively inhibit binding of [3H]cyclohexyladenosine, [3H]diethylphenylxanthine, [3H]phenylisopropyladenosine and [3H]diazepam. Both caffeine and theophylline are more potent as inhibitors of adenosine receptor ligand binding compared to [3H]diazepam binding. Theophylline was more potent than caffeine in its ability to compete with adenosine receptor ligand binding while the reverse was true for [3H]diazepam binding. The meaning of these results for the mode of action of methylxantine is discussed.
在人脑大脑皮质膜中研究了各种腺苷受体配体与[3H]地西泮的结合,以及它们对甲基黄嘌呤的抑制作用。咖啡因和茶碱竞争性抑制[3H]环己基腺苷、[3H]二乙苯基黄嘌呤、[3H]苯异丙基腺苷和[3H]地西泮的结合。与[3H]地西泮结合相比,咖啡因和茶碱作为腺苷受体配体结合的抑制剂更有效。在与腺苷受体配体结合的竞争能力方面,茶碱比咖啡因更有效,而在[3H]地西泮结合方面则相反。讨论了这些结果对甲基黄嘌呤作用模式的意义。