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对甲苯磺酸吡啶异吲哚酮对豚鼠回肠末端由ATP和嘌呤能刺激所产生收缩的影响。

Influence of pyridylisatogen tosylate on contractions produced by ATP and by purinergic stimulation in the terminal ileum of the guinea-pig.

作者信息

Kazić T, Milosavljević D

出版信息

J Pharm Pharmacol. 1977 Sep;29(9):542-5. doi: 10.1111/j.2042-7158.1977.tb11392.x.

Abstract

2-2'Pyridylisatogen tosylate (PIT), which antagonizes the inhibitory action of ATP in the taenia caeci, did not antagonize the excitatory effects of exogenous ATP and of purinergic stimulation of the terminal guinea-pig ileum. PIT (0-5--2-5 muM) potentiated the ATP-induced contractions and also the contractions produced by potassium chloride, though the potentiation could not be related to the dose in every experiment. The responses to noradrenaline, adrenaline and histamine were slightly inhibited. PIT also potentiated the contractions produced by electrical stimulation of intramural purinergic nerves when either an alternate or uniform stimulation pattern was used. The present results in which the preparation is contracted by ATP are opposite to those obtained with PIT on the taenia caeci, which is relaxed by ATP. This raises a question of duality or plurality of receptors for ATP.

摘要

对甲苯磺酸2-2'吡啶异红紫精(PIT)可拮抗ATP对盲肠带的抑制作用,但不能拮抗外源性ATP以及豚鼠回肠末端嘌呤能刺激的兴奋作用。PIT(0.5-2.5μM)增强了ATP诱导的收缩以及氯化钾引起的收缩,尽管在每个实验中这种增强作用与剂量无关。对去甲肾上腺素、肾上腺素和组胺的反应略有抑制。当采用交替或均匀刺激模式时,PIT还增强了壁内嘌呤能神经电刺激所产生的收缩。目前在该标本中ATP引起收缩的结果与在盲肠带上使用PIT所获得的结果相反,在盲肠带上ATP可使其松弛。这就提出了ATP受体的二元性或多元性问题。

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