Redl H, Vogl C, Schiesser A, Paul E, Thurnher M, Bahrami S, Schlag G
Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
J Lipid Mediat. 1990;2 Suppl:S195-201.
It has been reported that a platelet-activating factor (PAF) antagonist ONO-6240 had little effect on pulmonary hypertension and lung lymph in sheep injected with endotoxin lipopolysaccharide (LPS); consequently we evaluated a new PAF antagonist, BN 52021. Twelve adult sheep were surgically prepared for chronic study including lung lymph drainage. LPS (S. abortus equii, 36 ng/kg/h over 7 h) was then administered with (BN group) or without (control group) infusion (1 h before LPS) of the PAF antagonist BN 52021 (4 mg/kg/30 min). Comparison of the hemodynamic data between the control group and the BN group reveals an almost identical pattern. In contrast, we find differences in the pulmonary response of the two experimental groups. The early elevation of pulmonary artery pressure after LPS administration is less in the treatment group, as is the duration of pulmonary hypertension. Similarly, thromboxane levels are lower in the treated animals. The increases in lymph flow (LQ) and transvascular protein clearance (L/P X LQ) as well as the protein flux were less prominent in the treatment group. The mean lymph flow per hour was significantly higher in the control group. The mean lymph flow per hour was significantly higher in the control group, as were the corresponding parameters for clearance and protein flux. Thus the pulmonary vasculature and lung fluid balance disruption produced by LPS was markedly reduced by treatment with the PAF blocker.
据报道,血小板活化因子(PAF)拮抗剂ONO - 6240对注射内毒素脂多糖(LPS)的绵羊的肺动脉高压和肺淋巴几乎没有影响;因此,我们评估了一种新的PAF拮抗剂BN 52021。12只成年绵羊接受手术准备用于慢性研究,包括肺淋巴引流。然后在注射LPS(马流产沙门氏菌,7小时内36 ng/kg/h)时,给PAF拮抗剂BN 52021(4 mg/kg/30分钟)(BN组)或不给(对照组)(LPS注射前1小时)输注。对照组和BN组之间血流动力学数据的比较显示出几乎相同的模式。相比之下,我们发现两个实验组在肺部反应方面存在差异。治疗组在LPS给药后肺动脉压的早期升高幅度较小,肺动脉高压的持续时间也较短。同样,治疗动物体内的血栓素水平较低。治疗组中淋巴流量(LQ)、跨血管蛋白清除率(L/P×LQ)以及蛋白通量的增加不太明显。对照组每小时的平均淋巴流量显著更高。对照组每小时的平均淋巴流量显著更高,清除率和蛋白通量的相应参数也是如此。因此,用PAF阻滞剂治疗可显著减轻LPS引起的肺血管系统和肺液平衡破坏。