舒洛曲班选择性抑制猫周围血管床血栓素受体介导的反应。

Eicosanoids Pub Date : 1992-01-01
P Kvamme, R K Minkes, P J Kadowitz
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引用次数: 0

摘要

在控制猫后腿和肠系膜血管床血流的条件下,研究了舒洛曲班(bm13.177, SK&F 95587)的作用。注射血栓素(TX) A2模拟物U46619和U44069引起灌注压的剂量相关性升高。SK&F 95587给药后,血管收缩剂对TXA2模拟物的反应明显降低,剂量-反应曲线平行向右移动。去甲肾上腺素、苯肾上腺素、酪胺、内皮素-1、血管紧张素II、BAY K8644、乙酰胆碱、硝普钠、异丙肾上腺素、lemakalim、前列腺素(PG) E1和PGF2 α等通过多种机制改变血管阻力的药物的反应未被TXA2受体拮抗剂改变。然而,SK&F 95587降低了PGD2对肠系膜血管收缩剂的反应。本研究结果表明,SK&F 95587以竞争和选择性的方式阻断猫后躯循环中tx受体介导的反应,并减少肠系膜血管对TXA2模拟物和PGD2的反应。这些数据表明,该拮抗剂将有助于研究TXA2在猫全身血管床的生理和病理生理过程中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sulotroban selectively inhibits thromboxane-receptor-mediated responses in the peripheral vascular bed of the cat.

The effects of Sulotroban (BM 13.177, SK&F 95587) were investigated under conditions of controlled blood flow in the hindquarters and mesenteric vascular beds of the cat. Injections of the thromboxane (TX) A2 mimics, U46619 and U44069, caused dose-related increases in perfusion pressure. After administration of SK&F 95587, vasoconstrictor responses to the TXA2 mimics were reduced significantly, and the dose-response curves were shifted to the right in a parallel fashion. Responses to norepinephrine, phenylephrine, tyramine, endothelin-1, angiotensin II, BAY K8644, acetylcholine, sodium nitroprusside, isoproterenol, lemakalim, prostaglandin (PG) E1, and PGF2 alpha, agents which alter vascular resistance by a variety of mechanisms, were not changed by the TXA2 receptor antagonist. However, SK&F 95587 reduced mesenteric vasoconstrictor responses to PGD2. Results of the present study indicate that SK&F 95587 blocks TX-receptor-mediated responses in the hindquarters circulation of the cat in a competitive and selective manner and reduces mesenteric vascular responses to the TXA2 mimics, as well as PGD2. These data suggest that this antagonist would be useful in studies on the role of TXA2 in physiologic and pathophysiologic processes in the systemic vascular bed of the cat.

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