Underwood D C, Kriseman T, McNamara D B, Hyman A L, Kadowitz P J
J Appl Physiol (1985). 1987 Jun;62(6):2193-200. doi: 10.1152/jappl.1987.62.6.2193.
The effects of SQ 29,548, a thromboxane receptor antagonist, on airway responses were investigated in paralyzed, anesthetized, mechanically ventilated cats. Intravenous injections of the thromboxane and prostaglandin precursor, arachidonic acid (AA), and the thromboxane mimic, U 46619, produced dose-related increases in transpulmonary pressure and lung resistance and decreases in dynamic compliance. After administration of SQ 29,548 (0.5 mg/kg iv), bronchoconstrictor responses to AA were reduced by approximately 50%, whereas responses to U 46619 were reduced by approximately 90%. The cyclooxygenase inhibitor, sodium meclofenamate (2.5 mg/kg iv), blocked the component of the airway response to AA remaining after treatment with SQ 29,548. The thromboxane receptor antagonist had no significant effect on bronchoconstrictor responses to prostaglandins F2 alpha, and D2, methacholine, 5-hydroxytryptamine, histamine, or BAY K 8644, an agent that promotes calcium entry. Reductions in systemic arterial pressure in response to AA were enhanced by the thromboxane receptor antagonist and abolished by meclofenamate. SQ 29,548 had no effect on terminal enzyme activity in microsomal fractions from cat lung. These data support the hypothesis that AA-induced bronchoconstriction in the cat is mediated in large part by the actions of thromboxane A2. These data also suggest that U 46619 and U 44069 stimulate the same airway receptor as thromboxane A2 and mimic the bronchomotor effects of this hormone, which has not yet been isolated as a pure substance. These data demonstrate that SQ 29,548 is a selective thromboxane receptor antagonist in the airways of the closed-chest cat and may be a useful probe for studying responses to thromboxane A2 in physiological and pathophysiological processes in the lung.
在麻痹、麻醉、机械通气的猫身上研究了血栓素受体拮抗剂SQ 29,548对气道反应的影响。静脉注射血栓素和前列腺素前体花生四烯酸(AA)以及血栓素类似物U 46619,可使跨肺压和肺阻力呈剂量依赖性增加,动态顺应性降低。给予SQ 29,548(0.5毫克/千克静脉注射)后,对AA的支气管收缩反应降低约50%,而对U 46619的反应降低约90%。环氧化酶抑制剂甲氯芬那酸钠(2.5毫克/千克静脉注射)可阻断在用SQ 29,548治疗后剩余的对AA的气道反应成分。血栓素受体拮抗剂对前列腺素F2α、D2、乙酰甲胆碱、5-羟色胺、组胺或促进钙内流的药物BAY K 8644引起的支气管收缩反应无显著影响。血栓素受体拮抗剂增强了对AA的全身动脉压降低反应,而甲氯芬那酸钠可消除这种反应。SQ 29,548对猫肺微粒体部分的终末酶活性无影响。这些数据支持这样的假设,即猫中AA诱导的支气管收缩在很大程度上是由血栓素A2的作用介导的。这些数据还表明,U 46619和U 44069与血栓素A2刺激相同的气道受体,并模拟这种尚未作为纯物质分离出来的激素的支气管运动效应。这些数据表明,SQ 29,548是闭胸猫气道中的一种选择性血栓素受体拮抗剂,可能是研究肺生理和病理生理过程中对血栓素A2反应的有用探针。