Postdoctoral Fellow, Anesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Harvard Medical School at Massachusetts General Hospital, Boston, Massachusetts.
Instructor in Anesthesia, Anesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Harvard Medical School at Massachusetts General Hospital, Boston, Massachusetts.
Anesthesiology. 2012 Dec;117(6):1190-202. doi: 10.1097/ALN.0b013e318272d866.
The authors investigated whether transfusion with stored erythrocytes would increase tissue injury, inflammation, oxidative stress, and mortality (adverse effects of transfusing stored erythrocytes) in a murine model of hemorrhagic shock. They tested whether the adverse effects associated with transfusing stored erythrocytes were exacerbated by endothelial dysfunction and ameliorated by inhaling nitric oxide.
The authors studied mice fed a high-fat diet (HFD-fed; to induce endothelial dysfunction) or a standard diet for 4-6 weeks. Mice were subjected to 90 min of hemorrhagic shock, followed by resuscitation with leukoreduced syngeneic erythrocytes stored less than 24 h (fresh erythrocytes) or stored for 2 weeks (stored erythrocytes).
In standard-diet-fed mice at 2 h after resuscitation, transfusion with stored erythrocytes increased tissue injury more than transfusion with fresh erythrocytes. The adverse effects of transfusing stored erythrocytes were more marked in HFD-fed mice and associated with increased lactate levels and short-term mortality. Compared with fresh erythrocytes, resuscitation with stored erythrocytes was associated with a reduction in P50, increased plasma hemoglobin levels, and increased indices of inflammation and oxidative stress, effects that were exacerbated in HFD-fed mice. Inhaled nitric oxide reduced tissue injury, lactate levels, and indices of inflammation and oxidative stress and improved short-term survival in HFD-fed mice resuscitated with stored erythrocytes.
Resuscitation with stored erythrocytes adversely impacts outcome in mice with hemorrhagic shock, an effect that is exacerbated in mice with endothelial dysfunction. Inhaled nitric oxide reduces tissue injury and improves short-term survival in HFD-fed mice resuscitated with stored erythrocytes.
作者研究了在失血性休克的小鼠模型中,输注储存的红细胞是否会增加组织损伤、炎症、氧化应激和死亡率(输注储存红细胞的不良后果)。他们测试了输注储存的红细胞是否会加剧内皮功能障碍,并通过吸入一氧化氮来改善这种情况。
作者研究了高脂饮食(HFD 喂养;诱导内皮功能障碍)或标准饮食喂养 4-6 周的小鼠。小鼠经历 90 分钟的失血性休克,然后用少于 24 小时(新鲜红细胞)或储存 2 周(储存红细胞)的白细胞减少的同种异体红细胞复苏。
在复苏后 2 小时,标准饮食喂养的小鼠输注储存的红细胞比输注新鲜红细胞增加了更多的组织损伤。在 HFD 喂养的小鼠中,输注储存的红细胞的不良影响更为明显,与乳酸水平升高和短期死亡率增加有关。与新鲜红细胞相比,用储存的红细胞复苏与 P50 降低、血浆血红蛋白水平升高以及炎症和氧化应激指标增加有关,这些影响在 HFD 喂养的小鼠中更为明显。吸入一氧化氮可减少组织损伤、乳酸水平以及炎症和氧化应激的指标,并改善 HFD 喂养的小鼠用储存的红细胞复苏后的短期生存率。
在失血性休克的小鼠中,用储存的红细胞复苏会对结果产生不利影响,而在有内皮功能障碍的小鼠中,这种影响更为明显。吸入一氧化氮可减少组织损伤并提高 HFD 喂养的小鼠用储存的红细胞复苏后的短期生存率。