Donor Treatment With a Hypoxia‐Inducible Factor‐1 Agonist Prevents Donation After Cardiac Death Liver Graft Injury in a Rat Isolated Perfusion Model. Issue 3 (20th December 2017)

• Record Type: Journal Article
• Authors: Zhang, Xingjian; Liu, Zhongzhong; Xiao, Qi; Zeng, Cheng; Lai, Chin‐Hui; Fan, Xiaoli; Ye, Qifa; Wang, Yanfeng; Xiong, Yan
• Is Part Of: Artificial organs. Volume 42:Issue 3(2018)
• Page Start: 280
• Page End: 289
• Publication Date: 2017-12-20
• Subjects: Donation after cardiac death -- —Liver injury -- —Hypoxia‐inducible factor‐1α; Artificial organs -- Periodicals; 617.956
• DOI: 10.1111/aor.13005
• Languages: English
• ISSNs: 0160-564X

Abstract

Abstract: The protective role of hypoxia‐inducible factor‐1 (HIF‐1) against liver ischemia‐reperfusion injury has been well proved. However its role in liver donation and preservation from donation after cardiac death (DCD) is still unknown. The objective of this study was to test the hypothesis that pharmaceutical stabilization of HIF‐1 in DCD donors would result in a better graft liver condition. Male SD rats (6 animals per group) were randomly given the synthetic prolyl hydroxylase domain inhibitor FG‐4592 (Selleck, 6 mg/kg of body weight) or its vehicle (dimethylsulfoxide). Six hours later, cardiac arrest was induced by bilateral pneumothorax. Rat livers were retrieved 30 min after cardiac arrest, and subsequently cold stored in University of Wisconsin solution for 24 h. They were reperfused for 60 min with Krebs‐Henseleit bicarbonate buffer in an isolated perfused liver model, after which the perfusate and liver tissues were investigated. Pretreatment with FG‐4592 in DCD donors significantly improved graft function with increased bile production and synthesis of adenosine triphosphate, decreased perfusate liver enzyme release, histology injury scores and oxidative stress‐induced cell injury and apoptosis after reperfusion with the isolated perfused liver model. The beneficial effects of FG‐4592 is attributed in part to the accumulation of HIF‐1 and ultimately increased PDK1 production. Pretreatment with FG‐4592 in DCD donors resulted in activation of the HIF‐1 pathway and subsequently protected liver grafts from warm ischemia and cold‐stored injury. These data suggest that the pharmacological HIF‐1 induction may provide a clinically applicable therapeutic intervention to prevent injury to DCD allografts.