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Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation

机译:在止血带引起的肢体缺血再灌注损伤期间使用FTY720可减轻全身炎症

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摘要

Acute ischemia-reperfusion injury (IRI) of the extremities leads to local and systemic inflammatory changes which can hinder limb function and can be life threatening. This study examined whether the administration of the T-cell sequestration agent, FTY720, following hind limb tourniquet-induced skeletal muscle IRI in a rat model would attenuate systemic inflammation and multiple end organ injury. Sprague-Dawley rats were subjected to 1 hr of ischemia via application of a rubber band tourniquet. Animals were randomized to receive an intravenous bolus of either vehicle control or FTY720 15 min after band placement. Rats (n = 10/time point) were euthanized at 6, 24, and 72 hr post-IRI. Peripheral blood as well as lung, liver, kidney, and ischemic muscle tissue was analyzed and compared between groups. FTY720 treatment markedly decreased the number of peripheral blood T cells (p < 0.05) resulting in a decreased systemic inflammatory response and lower serum creatinine levels and had a modest but significant effect in decreasing the transcription of injury-associated target genes in multiple end organs. These findings suggest that early intervention with FTY720 may benefit the treatment of IRI of the limb. Further preclinical studies are necessary to characterize the short-term and long-term beneficial effects of FTY720 following tourniquet-induced IRI.
机译:四肢的急性缺血再灌注损伤(IRI)导致局部和全身性炎症改变,这可能会阻碍肢体功能并危及生命。这项研究检查了在大鼠模型中后肢止血带诱导的骨骼肌IRI后施用T细胞螯合剂FTY720是否能减轻全身炎症和多端器官损伤。通过应用橡皮筋止血带对Sprague-Dawley大鼠进行1小时的局部缺血。放置带后15分钟,将动物随机接受溶媒对照或FTY720的静脉推注。将大鼠(n = 10 /时间点)在IRI后的6、24和72小时处以安乐死。在各组之间分析和比较外周血以及肺,肝,肾和缺血性肌肉组织。 FTY720处理显着减少了外周血T细胞的数量(p <0.05),导致全身炎症反应降低和血清肌酐水平降低,并且在减少多个末端器官中与损伤相关的靶基因的转录方面具有适度但重要的作用。这些发现表明,早期使用FTY720进行干预可能有益于肢体IRI的治疗。进一步的临床前研究对于表征FTY720在止血带诱发的IRI后的短期和长期有益作用是必要的。

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