Magder Sheldon, Parthenis Dimitrios G, Ghouleh Imad Al
Critical Care Division, Royal Victoria Hospital, 687 Pine Ave W, Montreal, QC H3A 1A1, Canada.
Vascular Surgery of Nikaia, Peiraeous 18454, Greece.
Int J Mol Sci. 2015 Mar 25;16(4):6801-17. doi: 10.3390/ijms16046801.
Sepsis is associated with an increase in reactive oxygen species (ROS), however, the precise role of ROS in the septic process remains unknown. We hypothesized that treatment with EUK-134 (manganese-3-methoxy N,N'-bis(salicyclidene)ethylene-diamine chloride), a compound with superoxide dismutase and catalase activity, attenuates the vascular manifestations of sepsis in vivo. Pigs were instrumented to measure cardiac output and blood flow in renal, superior mesenteric and femoral arteries, and portal vein. Animals were treated with saline (control), lipopolysaccharide (LPS; 10 µg·kg-1·h-1), EUK-134, or EUK-134 plus LPS. Results show that an LPS-induced increase in pulmonary artery pressure (PAP) as well as a trend towards lower blood pressure (BP) were both attenuated by EUK-134. Renal blood flow decreased with LPS whereas superior mesenteric, portal and femoral flows did not change. Importantly, EUK-134 decreased the LPS-induced fall in renal blood flow and this was associated with a corresponding decrease in LPS-induced protein nitrotyrosinylation in the kidney. PO2, pH, base excess and systemic vascular resistance fell with LPS and were unaltered by EUK-134. EUK-134 also had no effect on LPS-associated increase in CO. Interestingly, EUK-134 alone resulted in higher CO, BP, PAP, mean circulatory filling pressure, and portal flow than controls. Taken together, these data support a protective role for EUK-134 in the renal circulation in sepsis.
脓毒症与活性氧(ROS)增加有关,然而,ROS在脓毒症过程中的具体作用尚不清楚。我们假设用EUK-134(锰-3-甲氧基-N,N'-双(水杨醛)乙二胺氯化物)进行治疗,一种具有超氧化物歧化酶和过氧化氢酶活性的化合物,可减轻体内脓毒症的血管表现。对猪进行仪器安装以测量心输出量以及肾动脉、肠系膜上动脉、股动脉和门静脉的血流量。动物分别接受生理盐水(对照)、脂多糖(LPS;10μg·kg-1·h-1)、EUK-134或EUK-134加LPS治疗。结果显示EUK-134减轻了LPS诱导肺动脉压(PAP)的升高以及血压(BP)降低的趋势。LPS使肾血流量减少,而肠系膜上动脉、门静脉和股动脉血流量未改变。重要的是,EUK-134减少了LPS诱导的肾血流量下降,这与肾脏中LPS诱导的蛋白质硝基酪氨酸化相应减少有关。LPS使PO2、pH、碱剩余和全身血管阻力下降,而EUK-134对此无影响。EUK-134对LPS相关的心输出量增加也无作用。有趣的是,单独使用EUK-134导致的心输出量、血压、肺动脉压、平均循环充盈压和门静脉血流量均高于对照组。综上所述,这些数据支持EUK-134在脓毒症肾循环中具有保护作用。