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[大鼠尾动脉和犬隐静脉水平嘌呤能P2受体的异质性]

[Heterogeneity of purinergic P2 receptors at the level of the caudal artery of the rat and the saphenous vein of the dog].

作者信息

Saiag B, Milon D, Guelou M C, Van den Driessche J, Rault B

出版信息

C R Seances Soc Biol Fil. 1987;181(2):168-77.

PMID:2957036
Abstract

Phentolamine (10(-5) M) and an inhibitor of the lipoxygenase pathway, nordihydroguaiaretic acid (N. D. G. A.; 8 10(-6) M) antagonized the ATP induced contraction but not antagonized the UTP induced contraction on both rat tail artery and dog saphenous vein. We conclude that the receptors to ATP are distinct from receptors to UTP and that the P2 purinoceptors are an heterogeneous group.

摘要

酚妥拉明(10⁻⁵M)和脂氧合酶途径抑制剂去甲二氢愈创木酸(NDGA;8×10⁻⁶M)可拮抗ATP诱导的大鼠尾动脉和狗隐静脉收缩,但不拮抗UTP诱导的收缩。我们得出结论,ATP受体与UTP受体不同,且P2嘌呤受体是一个异质群体。

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