Sodium thiosulfate-supplemented UW solution protects renal grafts against prolonged cold ischemia-reperfusion injury in a murine model of syngeneic kidney transplantation

被引:18
作者
Dugbartey, George J. [1 ,2 ,3 ,5 ]
Zhang, Max Y. [1 ,3 ]
Liu, Winnie [3 ]
Haig, Aaron [3 ]
McLeod, Patrick [1 ]
Arp, Jacqueline [1 ]
Sener, Alp [1 ,2 ,3 ,4 ]
机构
[1] Western Univ, Matthew Mailing Ctr Translat Transplant Studies, London Hlth Sci Ctr, London, ON, Canada
[2] Western Univ, London Hlth Sci Ctr, Dept Surg, Div Urol, London, ON, Canada
[3] Western Univ, London Hlth Sci Ctr, Multiorgan Transplant Program, London, ON, Canada
[4] Univ Western Ontario, Schulich Sch Med & Dent, Dept Microbiol & Immunol, London, ON, Canada
[5] Univ Ghana, Coll Hlth Sci, Sch Pharm, Dept Pharmacol & Toxicol, Legon, Accra, Ghana
关键词
Sodium thiosulfate (STS); Ischemia-reperfusion injury (IRI); Static cold storage (SCS); Kidney transplantation; Graft and recipient survival; HYDROGEN-SULFIDE; OXIDATIVE STRESS; RAT HEARTS; SURVIVAL; DIALYSIS; TIME; RECIPIENTS; REDUCTION; MORTALITY; APOPTOSIS;
D O I
10.1016/j.biopha.2021.112435
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Cold ischemia-reperfusion injury (IRI) is an inevitable event that increases post-transplant complications. We have previously demonstrated that supplementation of University of Wisconsin (UW) solution with non-FDA-approved hydrogen sulfide (H2S) donor molecules minimizes cold IRI and improves renal graft function after transplantation. The present study investigates whether an FDA-approved H2S donor molecule, sodium thiosulfate (STS), will have the same or superior effect in a clinically relevant rat model of syngeneic orthotopic kidney transplantation. Method: Thirty Lewis rats underwent bilateral nephrectomy followed by syngeneic orthotopic transplantation of the left kidney after 24-hour preservation in either UW or UW+STS solution at 4 degrees C. Rats were monitored to posttransplant day 14 and sacrificed to assess renal function (urine output, serum creatinine and blood urea nitrogen). Kidney sections were stained with H&E, TUNEL, CD68, and myeloperoxidase (MPO) to detect acute tubular necrosis (ATN), apoptosis, macrophage infiltration, and neutrophil infiltration. Result: UW+STS grafts showed significantly improved graft function immediately after transplantation, with improved recipient survival compared to UW grafts (p < 0.05). Histopathological examination revealed significantly reduced ATN, apoptosis, macrophage and neutrophil infiltration and downregulation of proinflammatory and pro-apoptotic genes in UW+STS grafts compared to UW grafts (p < 0.05). Conclusion: We show for the first time that preservation of renal grafts in STS-supplemented UW solution protects against prolonged cold IRI by suppressing apoptotic and inflammatory pathways, and thereby improving graft function and prolonging recipient survival. This could represent a novel clinically applicable therapeutic strategy to minimize the detrimental clinical outcome of prolonged cold IRI in kidney transplantation.
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页数:8
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