Su C
J Pharmacol Exp Ther. 1978 Feb;204(2):351-61.
The effect of ATP and its congeners on the adrenergic neuroeffector transmission was evaluated in isolated blood vessels of the rabbit. ATP, ADP, AMP and adenosine inhibited the contractile response of the portal vein to adrenergic nerve stimulation, with a threshold concentration of the order of 0.1 muM and ED50 of about 1 microM. These agents, but not papaverine, inhibited the nerve stimulation-induced response in preference to the norepinephrine- or serotonin-induced response in the portal and saphenous veins and pulmonary and ear arteries. In the portal vein labeled with [3H]norepinephrine, ATP diminished the nerve stimulation-induced efflux of tritiated material. This nucleotide also reduced the KCl-induced tritium efflux but not the tyramine induced-efflux in the [3H]norepinephrine-labeled thoracic aorta. ATP had no significant effect on the uptake of [3H]norepinephrine in the portal vein, ear artery and thoracic aorta. Indomethacin and theophylline partially blocked the inhibitory action of ATP on the neurogenic constrictor response in some of the ear artery and saphenous vein preparations. Desipramine, atropine, propanolol, haloperidol and 2,2'-pyridylisatogen, a blocking agent against ATP in the taenia coli, were without such antagonistic effect. The results are consistent with a proposed negative feedback modulator role of ATP or a related purine compound in adrenergic transmission.
在兔的离体血管中评估了ATP及其同系物对肾上腺素能神经效应传递的影响。ATP、ADP、AMP和腺苷抑制门静脉对肾上腺素能神经刺激的收缩反应,阈值浓度约为0.1μM,ED50约为1μM。这些药物而非罂粟碱优先抑制门静脉、隐静脉、肺动脉和耳动脉中神经刺激诱导的反应,而非去甲肾上腺素或5-羟色胺诱导的反应。在用[3H]去甲肾上腺素标记的门静脉中,ATP减少了神经刺激诱导的氚化物质外流。这种核苷酸也减少了[3H]去甲肾上腺素标记的胸主动脉中KCl诱导的氚外流,但不减少酪胺诱导的外流。ATP对门静脉、耳动脉和胸主动脉中[3H]去甲肾上腺素的摄取没有显著影响。吲哚美辛和茶碱部分阻断了ATP对某些耳动脉和隐静脉制剂中神经源性收缩反应的抑制作用。地昔帕明、阿托品、普萘洛尔、氟哌啶醇和2,2'-吡啶异吲哚酮(一种结肠带中ATP的阻断剂)没有这种拮抗作用。这些结果与ATP或相关嘌呤化合物在肾上腺素能传递中所提出的负反馈调节作用一致。