Cheng J B, Townley R G
Biochem Biophys Res Commun. 1984 Aug 16;122(3):949-54. doi: 10.1016/0006-291x(84)91183-5.
To determine whether the action of leukotriene E4 is mediated by its cross reaction with leukotriene D4 receptor sites, we compared [3H] leukotriene E4 and [3H]leukotriene D4 binding activities in selected tissues as well as their competition results in the guinea-pig crude lung membrane. We demonstrated good correlation of [3H]leukotriene E4 and [3H]leukotriene D4 binding activities among the tissues studied. A significant correlation was demonstrated between the ability of leukotriene C4, D4 and E4, FPL-55712 and arachidonic acid to inhibit lung [3H]leukotriene E4 and [3H]leukotriene D4 binding. These correlations suggest that leukotriene E4 binds to a site which is similar to or close to the leukotriene D4 receptor.
为了确定白三烯E4的作用是否通过其与白三烯D4受体位点的交叉反应介导,我们比较了[3H]白三烯E4和[3H]白三烯D4在选定组织中的结合活性以及它们在豚鼠粗制肺膜中的竞争结果。我们证明了在所研究的组织中,[3H]白三烯E4和[3H]白三烯D4的结合活性具有良好的相关性。白三烯C4、D4和E4、FPL-55712以及花生四烯酸抑制肺[3H]白三烯E4和[3H]白三烯D4结合的能力之间存在显著相关性。这些相关性表明白三烯E4与一个类似于或接近白三烯D4受体的位点结合。