前列腺素E1、前列腺素E0和spm206对离体人冠状动脉的影响。

L Bruch, A Kästner, P Ney, D Modersohn, G Baumann
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引用次数: 0

摘要

体外研究了PGE1、PGE0及稳定的PGE1类似物spm206对人心外膜冠状动脉的影响。等距测量离体动脉环的张力。预收缩后,绘制各化合物的浓度-响应曲线。PGE1和spm206引起浓度依赖性松弛,在高浓度时被收缩作用抵消。在PGE0中,即使在较低浓度下也会发生收缩作用。这种收缩被选择性血栓素A2拮抗剂SQ 29,548拮抗,导致所有三种化合物的等效松弛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of prostaglandin E1, prostaglandin E0 and SPM 206 on isolated human coronary arteries.

The effects of PGE1, PGE0 and the stable PGE1-analogue SPM 206 on human epicardial coronary arteries were studied in vitro. The tension of the isolated arterial rings was measured isometrically. After precontraction, concentration-response curves with the compounds were performed. PGE1 and SPM 206 elicited concentration-dependent relaxations which are counteracted by a contractile action in higher concentrations. In PGE0, the contractile action occurred even in lower concentrations. This contraction was antagonized by the selective thromboxane A2 antagonist SQ 29,548, resulting in an equipotent relaxation for all three compounds.

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