非低血压猪内毒素血症中血小板活化因子拮抗对肺损伤的调节作用。

Circulatory shock Pub Date : 1994-11-01
F M Abu-Zidan, S Walther, S Lennquist
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引用次数: 0

摘要

以36微克/千克/小时的剂量静脉滴注大肠杆菌内毒素诱导18头麻醉猪内毒素血症。9头猪接受新型血小板活化因子(PAF)拮抗剂BB-882预处理,剂量为33 mg/kg/hr,在内毒素治疗前30分钟开始,另外9头猪接受相似体积的载药。静脉晶体复苏维持正常血压。6头猪只注射了BB-882作为对照组。内毒素血症引起急性暂时性肺血管阻力增加300%,两组相同。最初的增加之后是第二次,更缓慢的,抗性上升,BB-882显著减弱(P < 0.01,重复测量方差分析)。BB-882对内毒素诱导的动脉脱氧和肺/胸顺应性下降没有显著影响。内毒猪接受BB-882治疗后,红细胞压积降低(P < 0.02)。与基线相比,对照组无明显变化。结果表明,PAF是非低血压猪内毒素血症早期肺功能障碍的次要决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of lung injury by platelet-activating factor antagonism in nonhypotensive porcine endotoxemia.

Endotoxemia was induced by intravenous infusion of Escherichia coli endotoxin in 18 anesthetized pigs in a dose of 36 micrograms/kg/hr. Nine pigs were pretreated with BB-882, a novel platelet-activating factor (PAF) antagonist, 33 mg/kg/hr, starting 30 min before endotoxin, and nine pigs received a similar volume of vehicle. Normotension was maintained with intravenous crystalloid resuscitation. Six pigs received only BB-882 and served as controls. Endotoxemia induced an acute transient 300% increase in pulmonary vascular resistance, identical in both groups. The initial increase was followed by a second, more gradual, rise in resistance, which was significantly attenuated by BB-882 (P < 0.01, repeated measurements ANOVA). Endotoxin-induced arterial deoxygenation and fall in lung/thorax compliance was not significantly altered by BB-882. Hematocrit was less in endotoxic pigs receiving BB-882 (P < 0.02). There were no significant changes compared to baseline in the control group. The results indicate that PAF is a minor determinant of early pulmonary dysfunction in nonhypotensive porcine endotoxemia.

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