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Differential effects of diadenosine phosphates on purinoceptors in the rat isolated perfused kidney

机译:磷酸二腺苷对大鼠离体灌注肾脏嘌呤受体的差异作用

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摘要

The activation of various purinoceptors in rat renal vasculature by P1,P2-diadenosine pyrophosphate (Ap2A), P1,P3-diadenosine triphosphate (Ap3A), P1,P4-diadenosine tetraphosphate (Ap4A), P1,P5-diadenosine pentaphosphate (Ap5A), P1,P6-diadenosine hexaphosphate (Ap6A) was studied by measuring their effects of perfusion pressure of a rat isolated perfused kidney.The vasoconstrictive response to Ap5A was completely due to P2X purinoceptor activation, that to Ap4A and Ap6 was P2X purinoceptor mediated to a large extent, as evidenced by the inhibitory effects of suramin and pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid tetrasodium (PPADS).The vasoconstrictive effects of Ap2A and Ap3A were mostly due to stimulation of A1-receptors, as shown by the inhibitory effect of 8-cyclopentyl-1,3-dipropylxanthine (DPCPX).The vasoconstrictive response to Ap6A was partially insensitive to A1 and P2X purinoceptor blockers.In raised tone preparations Ap2A and Ap3A evoked vasodilatation, which was blocked by the A2 receptor blocker, 3,7-dimethyl-1-propargylxanthine (DMPX).In raised tone preparations Ap4A evoked vasodilatation when the P2-purinoceptors were blocked by suramin.The activation of different purinoceptor subtypes by diadenosine phosphates critically depends on the number of phosphate groups.
机译:P1,P2-二腺苷焦磷酸(Ap2A),P1,P3-三腺苷三磷酸(Ap3A),P1,P4-二腺苷四磷酸(Ap4A),P1,P5-二腺苷五磷酸(Ap5A)激活各种嘌呤受体在大鼠肾血管中的活化通过测量大鼠离体肾脏的灌注压力来研究P1,P6-重氮腺苷六磷酸(Ap6A),对Ap5A的血管收缩反应完全是由P2X嘌呤受体激活引起的,对Ap4A和Ap6的血管收缩反应是P2X嘌呤受体介导的。苏拉明和吡ido醛-磷酸盐-6-偶氮苯基-2',4'-二磺酸四钠(PPADS)的抑制作用证明了这一程度.Ap2A和Ap3A的血管收缩作用主要是由于刺激了A1受体,如由8-环戊基-1,3-二丙基黄嘌呤(DPCPX)的抑制作用所显示。对Ap6A的血管收缩反应对A1和P2X嘌呤受体阻滞剂部分不敏感。在调剂中Ap2A和Ap3A引起血管舒张,这是在A2受体阻滞剂3,7-二甲基-1-炔丙基黄嘌呤(DMPX)的阻滞下,在苏拉明阻断P2-嘌呤受体时,Ap4A引起血管舒张。磷酸二氢腺苷对不同嘌呤受体亚型的激活主要取决于磷酸基团数。

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