Sevoflurane Attenuates Ischemia-Reperfusion Injury in a Rat Lung Transplantation Model

被引:51
|
作者
Ohsumi, Akihiro
Marseu, Katherine
Slinger, Peter
McRae, Karen
Kim, Hyunhee
Guan, Zehong
Hwang, David M.
Liu, Mingyao
Keshavjee, Shaf
Cypel, Marcelo
机构
[1] Univ Toronto, Latner Thorac Surg Res Labs, Univ Hlth Network, Toronto, ON, Canada
[2] Univ Toronto, Toronto Gen Hosp, Dept Anesthesiol, Toronto, ON, Canada
来源
ANNALS OF THORACIC SURGERY | 2017年 / 103卷 / 05期
关键词
MYOCARDIAL INFARCT SIZE; RANDOMIZED CONTROLLED-TRIAL; ISCHAEMIA/REPERFUSION INJURY; ISOFLURANE; ACTIVATION; DECREASES; SURGERY; KINASE; HEART; ISCHEMIA/REPERFUSION;
D O I
10.1016/j.athoracsur.2016.10.062
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Sevoflurane is one of the most commonly used volatile anesthetic agents with the fastest onset and offset, replacing isoflurane in modern anesthesiology. Preconditioning and postconditioning using volatile anesthetics can attenuate ischemia-reperfusion injury (IRI). However, no previous studies have evaluated the effect of sevoflurane in lung transplantation after cold ischemic injury. We aimed to study the effects of donor and recipient treatment with sevoflurane in a rat lung transplantation model. Methods. Lewis rats were allocated to four groups: control, PreC (preconditioning), PostC (postconditioning), and PreC + PostC. Donor rats in the PreC and PreC + PostC groups were exposed to 1.5% sevoflurane for 30 minutes before donor operation. Donor lungs were flushed with Perfadex and stored for 12 hours at 4 degrees C before transplantation. Recipients received orthotopic left lung transplantation. In the PostC and PreC + PostC groups, sevoflurane was initiated 2 minutes before reperfusion and maintained for 30 minutes. Two hours after reperfusion, lung function was evaluated, and samples were collected for histologic, inflammatory, and cell death assessment. Results. Preconditioning and postconditioning using sevoflurane significantly improved the oxygenation of lung grafts (partial arterial gas pressure of oxygen: 198 mm Hg in control, 406.5 mm Hg in PreC, 472.4 mm Hg in PostC, and 409.7 mm Hg in PreC + PostC, p < 0.0001) and reduced pulmonary edema. Sevoflurane treatment reduced levels of interleukin-1 beta, interleukin-6, and tumor necrosis factor-alpha. Moreover, sevoflurane significantly inhibited apoptotic cells by a decrease in cytochrome c release into cytosol and caspase-3 cleavage. Conclusions. Preconditioning or postconditioning of lungs using sevoflurane exhibits a significant protective effect against early phase of ischemia-reperfusion injury in a rat lung transplantation model. (C) 2017 by The Society of Thoracic Surgeons
引用
收藏
页码:1578 / 1586
页数:9
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