Semrad S D, Moore J N
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens 30602.
Res Vet Sci. 1987 Sep;43(2):137-42.
Thromboxane A2 may play a major role in circulatory shock. In some species, thromboxane synthetase inhibitors have a beneficial effect on shock induced by endotoxin, trauma, sepsis and administration of arachidonate. In some shock models, however, results with thromboxane synthetase inhibitors have been conflicting. The effect of UK-38,485, a selective thromboxane inhibitor, was evaluated in ponies injected with endotoxin intraperitoneally. Four groups of ponies were used to compare the effects of endotoxin alone, UK-38,485 alone, treatment with UK-38,485 before endotoxin challenge and treatment with UK-38,485 after endotoxin challenge. Haematological, metabolic, eicosanoid and clinical responses in each group were evaluated. The results indicated that UK-38,485 is an effective inhibitor of thromboxane A2 generation following endotoxin challenge. Prostacyclin values were elevated compared with baseline in ponies administered UK-38,485 and endotoxin. However, prostacyclin values were not significantly different from those of ponies receiving endotoxin alone. Furthermore, UK-38,485 failed to attenuate the haematological, metabolic and clinical manifestations commonly seen in the pony after endotoxin challenge.
血栓素A2可能在循环性休克中起主要作用。在某些物种中,血栓素合成酶抑制剂对内毒素、创伤、脓毒症和花生四烯酸盐给药诱导的休克具有有益作用。然而,在一些休克模型中,血栓素合成酶抑制剂的结果一直存在矛盾。在腹腔注射内毒素的小马中评估了选择性血栓素抑制剂UK-38,485的作用。使用四组小马比较单独使用内毒素、单独使用UK-38,485、在内毒素攻击前用UK-38,485治疗以及在内毒素攻击后用UK-38,485治疗的效果。评估了每组的血液学、代谢、类花生酸和临床反应。结果表明,UK-38,485是内毒素攻击后血栓素A2生成的有效抑制剂。与给予UK-38,485和内毒素的小马的基线相比,前列环素值升高。然而,前列环素值与仅接受内毒素的小马的前列环素值没有显著差异。此外,UK-38,485未能减轻小马在内毒素攻击后常见的血液学、代谢和临床表现。