The Benefits of Fibrinolysis Combined with Venous Systemic Oxygen Persufflation (VSOP) in a Rat Model of Donation after Circulatory Death and Orthotopic Liver Transplantation

• Published in: International journal of molecular sciences 2022-05, Vol.23 (9), p.5272
• Main Authors: Kröger, Nadja, Czigany, Zoltan, Jiang, Jipin, Afify, Mamdouh, Paschenda, Pascal, Nagai, Kazuyuki, Yagi, Shintaro, Tolba, René H
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Blood & organ donations; Cold storage; Cold tolerance; Cryopreservation; Cytokines; Damage tolerance; Fibrinolysis; Ischemia; ischemia-reperfusion injury; L-Lactate dehydrogenase; Lactate dehydrogenase; Lactic acid; Liver; Liver Transplantation; Liver transplants; Male; Measurement techniques; Microvasculature; Organ Preservation; Organs; orthotopic liver transplantation; oxygen; Oxygen - pharmacology; Perfusion; Rats; Rats, Inbred Lew; Streptokinase; Transplantation; Values; Velocity; VSOP
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23095272

Organ shortage has led to the increasing utilization of livers retrieved from donors after circulatory death (DCD). These pre-damaged organs are susceptible to further warm ischemia and exhibit minimal tolerance for cold storage. The aim was thus to examine the effects of fibrinolysis combined with Venous Systemic Oxygen Persufflation (VSOP) on the preservation of DCD livers in vivo. Livers of male Lewis rats were explanted after 45 min of warm ischemia, cold-stored for 18 h, and transplanted into a recipient animal. Livers were left untreated or underwent either VSOP or fibrinolysis via Streptokinase (SK) or received combined SK and VSOP. Combined treatment exhibited improved microvascular flow at 168 h (p = 0.0009) and elevated microperfusion velocity at 24 h post-transplantation (p = 0.0007). Combination treatment demonstrated increased portal venous flow (PVF) at 3 and 24 h post-transplantation (p = 0.0004, p < 0.0001), although SK and VSOP analogously achieved increases at 24 h (p = 0.0036, p = 0.0051). Enzyme release was decreased for combination treatment (p = 0.0002, p = 0.0223) and lactate dehydrogenase (LDH) measurements were lower at 24 h post-transplantation (p = 0.0287). Further supporting findings have been obtained in terms of serum cytokine levels and in the alterations of endothelial injury markers. The combination treatment of SK + VSOP might provide improved organ integrity and viability and may therefore warrant further investigation as a potential therapeutic approach in the clinical setting of DCD.