Sirois P, Roy S, Borgeat P
Prostaglandins. 1983 Jul;26(1):91-101. doi: 10.1016/0090-6980(83)90077-1.
The novel metabolites of arachidonic acid, leukotriene (LT) A4, B4, C4, D4 and E4 have potent myotropic activity on guinea-pig lung parenchymal strip in vitro. The receptors responsible for their action were characterized using desensitization experiments and the selective SRS-A antagonist, FPL-55712. During the continuous infusion of LTB4, the tissues became desensitized to LTB4 but were still responsive to histamine, LTA4, LTC4, LTD4 and LTE4. When LTD4 was infused continuously, the lung strips contracted to LTB4 and histamine but were no longer responsive to LTA4, LTC4, LTD4 and LTE4. Furthermore, FPL-55712 (10 ng ml-1 - 10 ug ml-1) produced dose-dependent inhibitions of LTA4, LTC4, LTD4 and LTE4 without inhibiting the contraction to LTB4 and histamine. On the basis of these results, it appears that the guinea-pig lung parenchyma may have one type of receptor for LTB4 and another for LTD4; LTA4, LTC4 and LTE4 probably act on the LTD4 receptor.
花生四烯酸的新型代谢产物白三烯(LT)A4、B4、C4、D4和E4在体外对豚鼠肺实质条具有强大的肌动活性。利用脱敏实验和选择性慢反应物质A(SRS - A)拮抗剂FPL - 55712对其作用所涉及的受体进行了表征。在持续输注白三烯B4(LTB4)的过程中,组织对LTB4产生了脱敏,但对组胺、白三烯A4(LTA4)、白三烯C4(LTC4)、白三烯D4(LTD4)和白三烯E4(LTE4)仍有反应。当持续输注LTD4时,肺条对LTB4和组胺收缩,但对LTA4、LTC4、LTD4和LTE4不再有反应。此外,FPL - 55712(10纳克/毫升 - 10微克/毫升)对LTA4、LTC4、LTD4和LTE4产生剂量依赖性抑制,而不抑制对LTB4和组胺的收缩。基于这些结果,豚鼠肺实质似乎可能有一种针对LTB4的受体和另一种针对LTD4的受体;LTA4、LTC4和LTE4可能作用于LTD4受体。