Satchell D G, Maguire M H
Eur J Pharmacol. 1982 Jul 30;81(4):669-72. doi: 10.1016/0014-2999(82)90358-2.
Inhibitory actions of three pairs of congeneric ATP and adenosine analogues on the isolated guinea-pig taenia coli were compared with the actions of ATP and adenosine. 8-Bromoadenosine, and 9-beta-D-arabinofuranosyladenosine (ara-adenosine) were inactive; 2'-deoxyadenosine was a weak partial agonist. 8-Bromo-ATP, ara-ATP and 2'-deoxy-ATP behaved like ATP and elicited rapid relaxations of the taenia but were not potentiated by dipyridamole. The divergent effects of identical structural modifications to ATP and adenosine provide evidence for separate adenosine and ATP receptors in the taenia coli.
比较了三对同属的ATP和腺苷类似物对豚鼠离体结肠带的抑制作用与ATP和腺苷的作用。8-溴腺苷和9-β-D-阿拉伯呋喃糖基腺苷(ara-腺苷)无活性;2'-脱氧腺苷是一种弱部分激动剂。8-溴-ATP、ara-ATP和2'-脱氧-ATP的作用与ATP相似,可引起结肠带快速松弛,但不受双嘧达莫增强。对ATP和腺苷进行相同结构修饰产生的不同效应为结肠带中存在独立的腺苷和ATP受体提供了证据。