体外膜肺氧合可改善脑死亡大鼠供体血液动力学不稳定的肝损伤。

IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL International Journal of Artificial Organs Pub Date : 2024-10-14 DOI:10.1177/03913988241278189
Jianbao Yang, Jian Li, Awang Zhuoga, Zeyuan Yu, Yongnan Li, Zuoyi Jiao
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引用次数: 0

摘要

背景:脑死亡后捐献(DBD)是肝移植的主要来源。然而,通过脑死亡后捐献获得的肝脏往往会因血流动力学不稳定而受损,从而可能影响移植结果。体外膜肺氧合(ECMO)作为供体肝脏取回的最佳技术,已在临床中得到应用。尽管ECMO已应用于临床,但其增强肝功能的确切机制仍难以捉摸。本研究旨在探讨 ECMO 如何改善脑死亡供体肝功能的机制:我们将 18 只雄性 Sprague-Dawley (SD) 大鼠(350 ± 50 克)随机分为三组:Con 组(n = 6)、DBD 辅助药物组(n = 6)和 DBD 辅助 ECMO 组(n = 6)。ECMO 3 小时后,大鼠被处死。我们评估并比较了 Con 组、DBD 辅助药物组和 DBD 辅助 ECMO 组大鼠的心率、血压、累积性肝损伤(通过 HE 和 TUNEL 染色评估)、血清 AST 和 ALT 水平、血清氧化应激因子(MDA、H2O2、SOD 和 8-OHdG)的变化以及相关炎症因子(白细胞介素 [IL]-1β、IL-6、IL-8 和 TNF-α)的血清浓度。随后,我们建立了大鼠正位肝移植(OLT)模型,并移植了通过上述方法获得的肝脏。观察了移植后肝脏的状态:结果:脑死亡 3 小时后,肝损伤恶化,血清转氨酶、炎症反应、氧化应激和 TUNEL 染色显著增加。令人震惊的是,ECMO 不仅稳定了脑死亡后的血流动力学,还减轻了肝损伤,从而缓解了肝移植后的状况:结论:ECMO 可稳定血液动力学,减轻炎症反应和氧化应激,从而提高肝移植移植物的质量。
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Extracorporeal membrane oxygenation ameliorate hepatic injury in brain death rat donors with hemodynamic instability.

Background: Donation after brain death (DBD) serves as the primary source for liver transplantation. However, livers obtained through DBD often incur damage due to unstable hemodynamics, potentially impacting transplantation outcomes. Extracorporeal Membrane Oxygenation (ECMO) emerges as an optimal technique for donor liver retrieval and has found application in clinical settings. Despite its clinical implementation, the precise mechanisms through which ECMO enhances liver functions remain elusive. This study aims to investigate the mechanisms underlying how ECMO ameliorates liver function in brain-dead donors.

Methods: We randomly assigned 18 male Sprague-Dawley (SD) rats (350 ± 50 g) into three groups: Con (n = 6), DBD-assisted drug (n = 6), and DBD-assisted ECMO (n = 6). After 3 h of ECMO, the rats were sacrificed. We assessed and compared changes in heart rate, blood pressure, cumulative liver damage (evaluated through HE and TUNEL staining), serum levels of AST and ALT, alterations in serum oxidative stress factors (MDA, H2O2, SOD, and 8-OHdG), and serum concentrations of related inflammatory factors (interleukin [IL]-1β, IL-6, IL-8, and TNF-α) among rats in the Con, DBD-assisted drug, and DBD-assisted ECMO groups. Subsequently, we established a rat orthotopic liver transplantation (OLT) model and transplanted livers obtained through the aforementioned methods. The post-transplantation status of the livers was observed.

Results: After 3 h of brain death, liver injury worsened, accompanied by a significant increase in serum transaminases, inflammatory responses, oxidative stress, and TUNEL staining. Strikingly, ECMO not only stabilized hemodynamics after DBD but also mitigated liver damage, leading to an alleviated status post liver transplantation.

Conclusions: ECMO stabilizes hemodynamics, attenuates inflammatory responses and oxidative stress, thereby enhancing the quality of liver grafts for transplantation.

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来源期刊
International Journal of Artificial Organs
International Journal of Artificial Organs 医学-工程:生物医学
CiteScore
3.40
自引率
5.90%
发文量
92
审稿时长
3 months
期刊介绍: The International Journal of Artificial Organs (IJAO) publishes peer-reviewed research and clinical, experimental and theoretical, contributions to the field of artificial, bioartificial and tissue-engineered organs. The mission of the IJAO is to foster the development and optimization of artificial, bioartificial and tissue-engineered organs, for implantation or use in procedures, to treat functional deficits of all human tissues and organs.
期刊最新文献
Design of eye phantom for optical coherence tomography angiography study. Correlation between circulating dephosphorylated uncarboxylated matrix Gla protein and vascular calcification in peritoneal dialysis patients. Investigation of the acute effect of the synthetic hemodialysis membrane on the expression of XRCC1 and PARP1 in chronic hemodialysis patients. Dynamic modeling of variable speed left ventricular assist devices coupled to the cardiovascular system. Extracorporeal membrane oxygenation ameliorate hepatic injury in brain death rat donors with hemodynamic instability.
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