Levi R, Burke J A, Guo Z G, Hattori Y, Hoppens C M, McManus L M, Hanahan D J, Pinckard R N
Circ Res. 1984 Feb;54(2):117-24. doi: 10.1161/01.res.54.2.117.
Platelet-activating factor is a novel phospholipid that has been implicated as an important mediator of acute allergic reactions. The intravenous administration of acetyl glyceryl ether phosphorylcholine, a pure, synthetic platelet-activating factor, causes electrocardiographic changes in the rabbit similar to those which are characteristic manifestations of systemic anaphylaxis. To determine whether platelet-activating factor contributes to anaphylactic cardiac dysfunction, we measured platelet-activating factor release from the sensitized guinea pig heart challenged in vitro with specific antigen and compared the resulting cardiac dysfunction with that induced by the injection of acetyl glyceryl ether phosphorylcholine into nonsensitized hearts. The results of these studies document that, during anaphylaxis in the isolated guinea pig heart, a platelet-activating factor is released into the coronary effluent that has physicochemical and functional properties similar to those of acetyl glyceryl ether phosphorylcholine. The intracardiac administration of acetyl glyceryl ether phosphorylcholine (10(-14) to 3 X 10(-9) mol) induced dose-related decreases in left ventricular contractile force (-5 to -85%) and coronary flow (-5 to -85%), as well as impaired atrioventricular conduction. The negative inotropic effect of acetyl glyceryl ether phosphorylcholine also was present in hearts perfused at constant flow. Although, in these hearts, acetyl glyceryl ether phosphorylcholine increased coronary resistance, which may have caused regional shunting and ischemia, it is unlikely that the negative inotropic effect of acetyl glyceryl ether phosphorylcholine was secondary to changes in coronary flow, since acetyl glyceryl ether phosphorylcholine also caused a dose-dependent negative inotropic effect in the electrically paced, noncoronary-perfused left atrium and right ventricular papillary muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
血小板活化因子是一种新型磷脂,被认为是急性过敏反应的重要介质。静脉注射乙酰甘油醚磷酸胆碱(一种纯的合成血小板活化因子)会使兔子出现心电图变化,类似于全身性过敏反应的特征性表现。为了确定血小板活化因子是否导致过敏性心脏功能障碍,我们测量了用特异性抗原体外攻击致敏豚鼠心脏时血小板活化因子的释放,并将由此产生的心脏功能障碍与向未致敏心脏注射乙酰甘油醚磷酸胆碱所诱导的心脏功能障碍进行比较。这些研究结果表明,在离体豚鼠心脏过敏反应期间,一种血小板活化因子释放到冠状动脉流出液中,其理化和功能特性与乙酰甘油醚磷酸胆碱相似。心内注射乙酰甘油醚磷酸胆碱(10^(-14)至3×10^(-9)摩尔)会导致左心室收缩力(-5%至-85%)和冠状动脉血流量(-5%至-85%)呈剂量相关下降,以及房室传导受损。乙酰甘油醚磷酸胆碱的负性肌力作用在恒流灌注的心脏中也存在。虽然在这些心脏中,乙酰甘油醚磷酸胆碱增加了冠状动脉阻力,这可能导致局部分流和缺血,但乙酰甘油醚磷酸胆碱的负性肌力作用不太可能继发于冠状动脉血流量的变化,因为乙酰甘油醚磷酸胆碱在电起搏、非冠状动脉灌注的左心房和右心室乳头肌中也产生了剂量依赖性的负性肌力作用。(摘要截断于250字)