PAF拮抗剂CV-3988和l - 652,731对豚鼠过敏反应肺和血液学反应的影响

Gisela Danko, Joseph E. Sherwood, Beverly Grissom, William Kreutner, Richard W. Chapman
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引用次数: 13

摘要

为了确定PAF在豚鼠过敏反应急性期的作用,我们测量了PAF输注对肺(支气管收缩)和血液学(血小板减少症、白细胞减少症、血液浓度、血浆TxB2升高)的反应,并将这些反应与主动和被动致敏豚鼠抗原暴露的影响进行了比较。我们还确定了结构无关的PAF拮抗剂CV-3988和l - 652,731对这些反应的影响。静脉给药PAF (50 - 400ng /kg)引起剂量相关的支气管收缩、血小板减少、白细胞减少、血液浓度和血浆TxB2升高。CV-3988(3和10 mg/kg,静脉滴注)和l - 652,731 (3 mg/kg,静脉滴注)预处理可不同程度地抑制paf诱导的这些反应。主动或被动致敏豚鼠静脉给予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TxB2未升高。此外,CV-3988 (10 mg/kg,静脉注射)和l - 652,731 (3 mg/kg,静脉注射)对过敏性支气管收缩、血小板减少、白细胞减少(主动致敏)和血液浓度没有抑制作用。PAF和过敏性过敏反应产生的不同变化以及PAF拮抗剂不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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the PAF antagonists, CV-3988 and L-652, 731 on the pulmonary and hematological responses to guinea pig anaphylaxis

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.

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