外atp酶对嘌呤能神经传递的调节

Charles Kennedy, Tim D. Westfall, Peter Sneddon
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引用次数: 21

摘要

体外atp酶在豚鼠输精管神经传递中嘌呤能组分的调节作用已用ARL 67156进行了研究,ARL 67156是一种新开发的体外atp酶抑制剂。ARL 67156以浓度依赖性的方式快速可逆地增强神经源性收缩。ARL 67156还能增强外源性ATP引起的收缩,但在p2 -嘌呤受体拮抗剂PPADS存在下,对稳定类似物α、β-亚甲基ATP或去甲肾上腺素和KCl的收缩没有影响。这些结果与ARL 67156对外链atp酶的抑制作用一致,表明外链atp酶调节豚鼠输精管嘌呤能神经传递。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of purinergic neurotransmission by ecto-ATPase

The role of ecto-ATPase in modulating the purinergic component of neurotransmission in the guinea-pig vas deferens has been investigated using ARL 67156, a recently developed inhibitor of ecto-ATPase. ARL 67156 rapidly and reversibly potentiated neurogenic contractions in a concentration-dependent manner. ARL 67156 also potentiated contractions evoked by exogenous ATP, but had no effect on those to the stable analogue α,β-methyleneATP or on those to noradrenaline and KCl in the presence of the P2-purinoceptor antagonist PPADS. These results are consistent with an inhibitory action of ARL 67156 on ecto-ATPase and suggest that ecto-ATPase modulates purinergic neurotransmission in the guinea-pig vas deferens.

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