Bienvenu K, Granger D N
Department of Physiology, LSU Medical Center, Shreveport 71130-3932.
Blood Cells. 1993;19(2):279-88; discussion 288-9.
Reperfusion of ischemic tissues is associated with a sequence of events that closely resembles an acute inflammatory response. The increased leukocyte rolling, adherence and emigration in postcapillary venules elicited by ischemia/reperfusion appear to result from an accumulation of mediators such as platelet activating factor and leukotriene B4. These adhesive interactions between circulating leukocytes and venular endothelium are modulated by adhesion glycoproteins expressed on the surface of activated neutrophils and endothelial cells, reactive oxygen metabolites and granule-associated proteins produced by neutrophils, and by hydrodynamic forces generated within the microcirculation. Therapeutic interventions directed against either of these factors may prove to be effective in reducing ischemia/reperfusion injury.
缺血组织的再灌注与一系列类似于急性炎症反应的事件相关。缺血/再灌注引起的毛细血管后微静脉中白细胞滚动、黏附和移出增加,似乎是由血小板活化因子和白三烯B4等介质的积累所致。循环白细胞与微静脉内皮之间的这些黏附相互作用,受到活化中性粒细胞和内皮细胞表面表达的黏附糖蛋白、中性粒细胞产生的活性氧代谢产物和颗粒相关蛋白,以及微循环内产生的流体动力的调节。针对这些因素中的任何一个进行治疗干预,可能都被证明对减轻缺血/再灌注损伤有效。