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嘌呤和嘧啶核苷酸对主动脉平滑肌细胞前列环素释放的刺激作用。

Stimulation of prostacyclin release from aortic smooth muscle cells by purine and pyrimidine nucleotides.

作者信息

Demolle D, Lagneau C, Boeynaems J M

机构信息

Institute of Interdisciplinary Research, School of Medicine, Free University of Brussels, Belgium.

出版信息

Eur J Pharmacol. 1988 Oct 18;155(3):339-43. doi: 10.1016/0014-2999(88)90526-2.

Abstract

ATP and ATP gamma S(10-100 microM) stimulated the release of prostacyclin (PGI2) from bovine aortic smooth muscle cells. This effect was reproduced by UTP, ITP and partially by GTP. ADP and ADP beta S, the P2X-selective agonist alpha, beta-methylene ATP (APCPP), AMP and adenosine were all inactive. This effect of ATP gamma S was not inhibited by Reactive Blue 2, an antagonist of P2Y receptors. The stimulation of PGI2 production in aortic smooth muscle cells by these nucleotides thus seems to involve receptors distinct from both P2X and P2Y subtypes, which are responsible for smooth muscle contraction and PGI2 release from endothelial cells, respectively.

摘要

ATP和ATPγS(10 - 100微摩尔)刺激牛主动脉平滑肌细胞释放前列环素(PGI2)。UTP、ITP以及部分GTP也能产生这种效应。ADP、ADPβS、P2X选择性激动剂α,β-亚甲基ATP(APCPP)、AMP和腺苷均无活性。ATPγS的这种效应不受P2Y受体拮抗剂活性蓝2的抑制。因此,这些核苷酸对主动脉平滑肌细胞中PGI2生成的刺激作用似乎涉及不同于P2X和P2Y亚型的受体,P2X和P2Y亚型分别负责平滑肌收缩和内皮细胞释放PGI2。

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