Ikram Ben Jeddou, Mohamed Amine Zaouali, Roua Chaabani, Sameh Belgacem, Amira Cherif, Hassen Ben Abdennebi
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Liver injury, graft function, energy balance, autophagy, oxidative stress as well as inflammatory response were assessed.</p><p><strong>Results: </strong>Flushing hepatic grafts with PEG35-enriched RLS resulted in decreased transaminase levels after cold ischemia. The improved graft function was evidenced by increased bile flow, enhanced BSP clearance, and reduced vascular resistance in these flushed grafts. Phospho-AMPK protein expression, as well as LC3B gene and protein expression were significantly increased compared to those unflushed and flushed only with RLS. PEG35-enriched RLS also maintained the oxidative state, as indicated by reduced activities of antioxidant enzymes and decreased MDA concentration. Additionally, this graft rinse solution down-regulated the inflammatory response by inhibiting the expression of genes involved in the HMGB-1/NF-κB/TNF-α signaling pathway.</p><p><strong>Conclusion: </strong>These data strongly suggest that rinsing liver grafts with PEG35-enriched RLS prior to reperfusion represents a simple and cost-effective strategy to enhance liver functional recovery after cold IR injury. 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引用次数: 0
摘要
背景:肝移植(LT)过程中冷缺血再灌注(IR)损伤是影响肝移植功能的多因素过程。虽然在再灌注前冲洗肝移植物已经有了很好的研究,但预防冷IR损伤的最佳移植物冲洗溶液仍未明确。本研究的目的是评估聚乙二醇PM 35000 Da (PEG35)与乳酸溶液(RLS)的新型冲洗液是否能减轻Wistar大鼠的冷IR损伤。方法:分离肝脏,保存24小时,在体外再灌注RLS或富含peg35的RLS之前立即冲洗肝脏。评估肝损伤、移植物功能、能量平衡、自噬、氧化应激和炎症反应。结果:富peg35 RLS的肝移植物在冷缺血后转氨酶水平降低。在这些冲洗过的移植物中,胆汁流量增加,BSP清除增强,血管阻力降低,证明了移植物功能的改善。与未冲洗和仅冲洗的RLS相比,Phospho-AMPK蛋白表达、LC3B基因和蛋白表达均显著升高。富含peg35的RLS也保持了氧化状态,表现为抗氧化酶活性降低,MDA浓度降低。此外,该移植物冲洗液通过抑制HMGB-1/NF-κB/TNF-α信号通路相关基因的表达来下调炎症反应。结论:这些数据强烈提示,在再灌注前用富含peg35的RLS冲洗肝移植物是一种简单且经济有效的策略,可以增强冷IR损伤后的肝功能恢复。这种方法可以作为临床应用中RLS的可行替代方法,强调需要进一步研究以探索其更广泛的意义。
Mitigating hepatic ischemia and reperfusion injury with polyethylene glycol-enriched Ringer's lactate fluid: insights from an isolated perfused rat model.
Background: Cold ischemia-reperfusion (IR) injury is a multifactorial process detrimental to liver graft function during liver transplantation (LT). Although flushing hepatic grafts prior to reperfusion have been well explored, the optimal graft rinse solution to prevent cold IR injury remains largely undefined. The aim of this study was to evaluate whether a new rinse solution combining polyethylene glycol PM 35,000 Da (PEG35) with lactated solution (RLS) could mitigate cold IR injury in Wistar rats.
Methods: Livers were isolated, preserved for 24 h and flushed immediately before ex vivo reperfusion with either RLS or PEG35-enriched RLS. Liver injury, graft function, energy balance, autophagy, oxidative stress as well as inflammatory response were assessed.
Results: Flushing hepatic grafts with PEG35-enriched RLS resulted in decreased transaminase levels after cold ischemia. The improved graft function was evidenced by increased bile flow, enhanced BSP clearance, and reduced vascular resistance in these flushed grafts. Phospho-AMPK protein expression, as well as LC3B gene and protein expression were significantly increased compared to those unflushed and flushed only with RLS. PEG35-enriched RLS also maintained the oxidative state, as indicated by reduced activities of antioxidant enzymes and decreased MDA concentration. Additionally, this graft rinse solution down-regulated the inflammatory response by inhibiting the expression of genes involved in the HMGB-1/NF-κB/TNF-α signaling pathway.
Conclusion: These data strongly suggest that rinsing liver grafts with PEG35-enriched RLS prior to reperfusion represents a simple and cost-effective strategy to enhance liver functional recovery after cold IR injury. This approach could serve as a viable alternative to RLS in clinical applications, highlighting the need for further research to explore its broader implications.
期刊介绍:
BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.