Fedan J S, Hogaboom G K, O'Donnell J P
Eur J Pharmacol. 1986 Oct 7;129(3):279-91. doi: 10.1016/0014-2999(86)90438-3.
Some structural requirements which are important for the contractile activity of adenine nucleotides at P2-purinergic receptors in the guinea-pig isolated vas deferens were examined. The consequences of deletions, substitutions and isosteric rearrangements in 1-N, C-2, C-8, N-9 and N6 of adenine, in the ribose hydroxyls, and in the polyphosphate chain were examined. Several kinds of effects on activity were observed, including potentiation of responses, losses in activity, modifications of response duration, and transitions from biphasic concentration-response curves, which are characteristic of ATP, to monophasic curves. Generally, deletions and substitutions to adenine reduced activity. Ribose modifications were better-tolerated. The presence of 5'-phosphate or phosphorothioate moieties was required for maximum activity. A comparison of the present results with previous reports indicates that certain modifications to ATP result in similar effects in both the vas deferens and urinary bladder, which are opposite those which occur in the taenia coli.
研究了一些对豚鼠离体输精管中P2 -嘌呤能受体处腺嘌呤核苷酸收缩活性很重要的结构要求。研究了腺嘌呤的1 - N、C - 2、C - 8、N - 9和N6、核糖羟基以及多磷酸链中缺失、取代和等排重排的后果。观察到了几种对活性的影响,包括反应增强、活性丧失、反应持续时间改变以及从ATP特有的双相浓度 - 反应曲线转变为单相曲线。一般来说,腺嘌呤的缺失和取代会降低活性。核糖修饰的耐受性更好。最大活性需要5'-磷酸或硫代磷酸部分的存在。将目前的结果与先前的报告进行比较表明,对ATP的某些修饰在输精管和膀胱中产生相似的效果,这与在结肠带中发生的效果相反。