Woodman O L, Dusting G J
Eur J Pharmacol. 1982 Dec 17;86(1):125-8. doi: 10.1016/0014-2999(82)90410-1.
In the anaesthetized dog LTC4, LTD4 (0.3-10 micrograms, injected into the coronary artery) and the thromboxane-mimetic U46619 (5-10 micrograms) decreased coronary blood flow. LTE4 (1-10 micrograms), however, did not affect coronary blood flow. The vasoconstrictor responses to LTC4, LTD4 or U46619 were not altered by the cyclo-oxygenase inhibitor indomethacin (5 mg/kg i.v.). LTC4 and LTD4 did not stimulate the release of any prostaglandin-like substance into the pericardial fluid. It is concluded that LTC4 and LTD4 are able to produce coronary vasoconstriction in vivo independent of the production of any cyclo-oxygenase metabolites of arachidonic acid.
在麻醉犬中,白三烯C4(LTC4)、白三烯D4(LTD4,0.3 - 10微克,注入冠状动脉)和血栓素类似物U46619(5 - 10微克)可降低冠状动脉血流量。然而,白三烯E4(LTE4,1 - 10微克)对冠状动脉血流量无影响。环氧化酶抑制剂吲哚美辛(5毫克/千克静脉注射)不会改变对LTC4、LTD4或U46619的血管收缩反应。LTC4和LTD4不会刺激任何类前列腺素物质释放到心包液中。得出的结论是,LTC4和LTD4能够在体内产生冠状动脉血管收缩,而与花生四烯酸的任何环氧化酶代谢产物的产生无关。