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二磷酸腺苷对大鼠离体灌注肾脏中嘌呤受体的不同作用。

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

作者信息

van der Giet M, Khattab M, Börgel J, Schlüter H, Zidek W

机构信息

Ruhr-Universität Bochum, Marienhospital Herne, Med. Klinik I, Germany.

出版信息

Br J Pharmacol. 1997 Apr;120(8):1453-60. doi: 10.1038/sj.bjp.0701074.

Abstract
  1. 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. 2. 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). 3. 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). 4. The vasoconstrictive response to Ap6A was partially insensitive to A1 and P2x purinoceptor blockers. 5. In raised tone preparations Ap2A and Ap3A evoked vasodilatation, which was blocked by the A2 receptor blocker, 3,7-dimethyl-1-propargylxanthine (DMPX). 6. In raised tone preparations Ap4A evoked vasodilatation when the P2-purinoceptors were blocked by suramin. 7. The activation of different purinoceptor subtypes by diadenosine phosphates critically depends on the number of phosphate groups.
摘要
  1. 通过测量P1,P2 - 二磷酸腺苷(Ap2A)、P1,P3 - 三磷酸腺苷(Ap3A)、P1,P4 - 四磷酸腺苷(Ap4A)、P1,P5 - 五磷酸腺苷(Ap5A)、P1,P6 - 六磷酸腺苷(Ap6A)对大鼠离体灌注肾脏灌注压力的影响,研究了它们对大鼠肾血管中各种嘌呤受体的激活作用。2. 对Ap5A的血管收缩反应完全是由于P2x嘌呤受体激活所致,对Ap4A和Ap6的反应在很大程度上是由P2x嘌呤受体介导的,这可通过苏拉明和磷酸吡哆醛 - 6 - 偶氮苯 - 2',4' - 二磺酸四钠(PPADS)的抑制作用得以证明。3. Ap2A和Ap3A的血管收缩作用主要是由于对A1受体的刺激,这可通过8 - 环戊基 - 1,3 - 二丙基黄嘌呤(DPCPX)的抑制作用显示出来。4. 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。5. 在肌张力升高的制剂中,Ap2A和Ap3A引起血管舒张,这被A2受体阻滞剂3,7 - 二甲基 - 1 - 丙炔基黄嘌呤(DMPX)阻断。6. 在肌张力升高的制剂中,当P2 - 嘌呤受体被苏拉明阻断时,Ap4A引起血管舒张。7. 磷酸腺苷对不同嘌呤受体亚型的激活作用关键取决于磷酸基团的数量。

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