Danko G, Sherwood J E, Grissom B, Kreutner W, Chapman R W
Department of Allergy and Inflammation, Schering-Plough Corporation, Bloomfield, New Jersey 07003.
Pharmacol Res Commun. 1988 Sep;20(9):785-98. doi: 10.1016/s0031-6989(88)80717-3.
To define the role of PAF in the acute phase of guinea pig anaphylaxis, we have measured the pulmonary (bronchoconstrictor) and hematological (thrombocytopenia, leukopenia, hemoconcentration, plasma TxB2 increase) responses to PAF infusion and compared these responses to the effect of antigen exposure in actively and passively sensitized guinea pigs. We have also determined the effect of the structurally unrelated PAF antagonists, CV-3988 and L-652,731 on these responses. Intravenous administration of PAF (50-400 ng/kg) caused a dose-related bronchoconstriction, thrombocytopenia, leukopenia, hemoconcentration and increase in plasma TxB2. These PAF-induced responses were inhibited, to a variable degree, by pretreatment with CV-3988 (3 and 10 mg/kg, i.v.) and L-652,731 (3 mg/kg, i.v.). Intravenous administration of ovalbumin to actively or passively sensitized guinea pigs caused bronchoconstriction, thrombocytopenia, leukopenia and hemoconcentration, but there was no increase in TxB2. Moreover, the anaphylactic bronchoconstriction, thrombocytopenia, leukopenia (actively sensitized) and hemoconcentration were not inhibited by CV-3988 (10 mg/kg, i.v.) and L-652,731 (3 mg/kg, i.v.). The different profile of changes produced by PAF and allergic anaphylaxis and the failure to alter the responses to allergic anaphylaxis with PAF antagonists suggest that PAF is not an important mediator of the acute phase of guinea pig anaphylaxis.
为了确定血小板活化因子(PAF)在豚鼠过敏反应急性期的作用,我们测量了静脉注射PAF后肺部(支气管收缩)和血液学方面(血小板减少、白细胞减少、血液浓缩、血浆血栓素B2增加)的反应,并将这些反应与主动和被动致敏豚鼠接触抗原后的效应进行了比较。我们还测定了结构不相关的PAF拮抗剂CV - 3988和L - 652,731对这些反应的影响。静脉注射PAF(50 - 400 ng/kg)可引起剂量相关的支气管收缩、血小板减少、白细胞减少、血液浓缩以及血浆血栓素B2增加。预先静脉注射CV - 3988(3和10 mg/kg)和L - 652,731(3 mg/kg)可不同程度地抑制这些PAF诱导的反应。对主动或被动致敏的豚鼠静脉注射卵清蛋白可引起支气管收缩、血小板减少、白细胞减少和血液浓缩,但血栓素B2没有增加。此外,CV - 3988(10 mg/kg,静脉注射)和L - 652,731(3 mg/kg,静脉注射)不能抑制过敏反应性支气管收缩、血小板减少、白细胞减少(主动致敏)和血液浓缩。PAF和过敏性过敏反应产生的不同变化模式以及PAF拮抗剂未能改变对过敏性过敏反应的反应表明,PAF不是豚鼠过敏反应急性期的重要介质。