Barst S, Mullane K
Eur J Pharmacol. 1985 Aug 27;114(3):383-7. doi: 10.1016/0014-2999(85)90384-x.
Myocardial infarction was induced in rabbits and 24-48 h later the hearts were removed and perfused in vitro with the coronary effluent superfusing a guinea-pig ileum. The formyl tripeptide (FMLP: 10-100 ng) induced the dose-related release of a substance which contracted the ileum, an effect mimicked by exogenous LTD4 (2-200 ng), blocked by FPL 55712 (2 micrograms/ml) and inhibited with BW755C (2 micrograms/ml) but not indomethacin (1 micrograms/ml). The delayed release of this LTD4-like material may suggest a role in the complications accompanying myocardial infarction.
在兔身上诱发心肌梗死,24 - 48小时后取出心脏,在体外将冠状动脉流出液灌注到豚鼠回肠上进行灌注。甲酰三肽(FMLP:10 - 100纳克)诱导一种使回肠收缩的物质呈剂量相关释放,外源性白三烯D4(LTD4,2 - 200纳克)可模拟该效应,FPL 55712(2微克/毫升)可阻断该效应,BW755C(2微克/毫升)可抑制该效应,但吲哚美辛(1微克/毫升)无此作用。这种类LTD4物质的延迟释放可能提示其在心肌梗死相关并发症中发挥作用。