From the US Army Institute of Surgical Research, JBSA Fort Sam Houston, TX, United States.
From the US Army Institute of Surgical Research, JBSA Fort Sam Houston, TX, United States.
Vet J. 2024 Oct;307:106221. doi: 10.1016/j.tvjl.2024.106221. Epub 2024 Aug 8.
Hemorrhagic shock and subsequent resuscitation can cause significant dysregulation of critical systems, including the vascular endothelium. Following hemorrhage, the endothelial lining (glycocalyx) can shed, causing release of glycocalyx components, endothelial activation, and systemic inflammation. A canine model of hemorrhagic shock was used to evaluate five resuscitation fluids, including Lactated Ringers+Hetastarch, Whole Blood (WB), Fresh Frozen Plasma+packed Red Blood Cells (FFP+pRBC), and two hemoglobin-based oxygen carrier (HBOC) fluids, for their impact on glycocalyx shedding. Under anesthesia, purpose-bred adult canines were instrumented and subjected to a controlled hemorrhage with blood being drawn until a mean arterial pressure of <50 mmHg was reached or 40 % of the estimated blood volume was removed. Canines were left in shock for 45 mins before being resuscitated with one of the resuscitation fluids over 30 mins. Following resuscitation, the dogs were monitored up to 2 weeks. Following an additional 3-4 weeks for washout, the canines repeated the protocol, undergoing each resuscitation fluid individually. Blood samples were collected during each round at various timepoints for serum isolation, which was used for detection of glycocalyx biomarker. Comparison of baseline and post-hemorrhage alone showed a significant reduction in serum protein (p<0.0001), heparan sulfate (p<0.001), and syndecan-1 (p<0.0001) concentrations, and a significant increase in hyaluronan (p<0.0001) concentration. Intercomparisons of resuscitation fluids indicated minimal differences in glycocalyx markers over time. Comparisons within each fluid showed dynamic responses in glycocalyx biomarkers over time. Relative to individual baselines, syndecan-1 was significantly reduced after resuscitation in most cases (p<0.0001), excluding WB and FFP+pRBC. In all cases, VE-cadherin was significantly elevated at 24 hr compared to baseline (p<0.001). Hyaluronan was significantly elevated by 3 hr in all cases (p<0.01), except for HBOC fluids. Total glycosaminoglycans were significantly reduced only at 3 hr (p<0.001) for non-HBOC fluids. Similarly, heparan sulfate was significantly reduced with all fluids between resuscitation and 24 hr (p<0.01), except WB. The temporal changes in canine glycocalyx biomarkers were atypical of hemorrhage response in other species. This suggests that the hemorrhage lacked severity and/or typical glycocalyx biomarkers do not reflect the canine endothelium compared to other species. Further research is needed to characterize the canine endothelium and the response to resuscitation fluids.
失血性休克及随后的复苏可导致关键系统出现显著失调,包括血管内皮。出血后,内皮衬里(糖萼)可能会脱落,导致糖萼成分释放、内皮激活和全身炎症。使用犬失血性休克模型来评估五种复苏液,包括乳酸林格氏液+羟乙基淀粉、全血(WB)、新鲜冷冻血浆+浓缩红细胞(FFP+pRBC)和两种血红蛋白基氧载体(HBOC)液体,以评估它们对糖萼脱落的影响。在麻醉下,对专门饲养的成年犬进行仪器操作,并进行控制性出血,直到平均动脉压<50mmHg 或估计血容量的 40%被抽出。犬在休克中停留 45 分钟,然后用其中一种复苏液进行 30 分钟的复苏。复苏后,狗被监测长达 2 周。在 3-4 周的洗脱期后,犬重复该方案,分别使用每种复苏液。在每个循环的不同时间点采集血液样本进行血清分离,用于检测糖萼生物标志物。与基线和单独出血后相比,血清蛋白(p<0.0001)、硫酸乙酰肝素(p<0.001)和连接蛋白-1(p<0.0001)浓度显著降低,透明质酸(p<0.0001)浓度显著升高。复苏液的相互比较表明,糖萼标志物随时间的变化差异很小。每种液体中的比较显示,糖萼生物标志物随时间的动态反应。与个体基线相比,大多数情况下(p<0.0001),复苏后连接蛋白-1显著降低,除 WB 和 FFP+pRBC 外。在所有情况下,与基线相比,VE-钙粘蛋白在 24 小时时显著升高(p<0.001)。透明质酸在所有情况下均在 3 小时时显著升高(p<0.01),除 HBOC 液体外。只有非 HBOC 液体在 3 小时时总糖胺聚糖显著降低(p<0.001)。同样,肝素硫酸在复苏和 24 小时之间所有液体中均显著降低(p<0.01),除 WB 外。犬糖萼生物标志物的时间变化与其他物种的出血反应不同。这表明,与其他物种相比,这种出血缺乏严重性,而且典型的糖萼生物标志物不能反映犬的内皮。需要进一步研究来描述犬的内皮和对复苏液的反应。