Toggle Main Menu Toggle Search

Open Access padlockePrints

Ischemia-reperfusion injury in cadaveric nonheart beating, cadaveric heart beating and live donor renal transplants

Lookup NU author(s): Muhammed Gok, Dr Brian Shenton, Dr David Mantle, David Rix, Bryon Jaques, Professor Naeem Soomro, Professor Derek Manas, David Talbot

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

Purpose: Ischemia-reperfusion injury is gaining importance in transplantation as being responsible for allograft dysfunction. Ischemia occurs during kidney procurement, which is shortest in LDs, and prolonged in cadaveric HBDs and NHBDs. Materials and Methods: Renal transplants from 17 LDs, 15 HBDs and 19 NHBDs were assessed during reperfusion for biochemical markers of ischemia-reperfusion injury and assessed clinically. Central venous blood sampling was assayed for free radicals using electron spin resonance and tissue injury biomarkers, namely lactate dehydrogenase, fatty acid binding protein, alanine aminopeptidase, lactate and total antioxidants. Results: The return to stable renal function was more rapid in LD renal transplants, while recovery continued from 3 months after hospital discharge in NHBD renal transplants. Injury markers, such as lactate dehydrogenase, fatty acid binding protein, alanine aminopeptidase and lactate, were raised at the time of reperfusion, especially in NHBD renal transplants. Free radical release measured by electron spin resonance showed 2 phase release, that is early (0 to 10-minute) and late (20 to 40-minute) release. In NHBD, HBD and LD renal transplants the index of free radical release in the early phase was 1.43, 1.36 and 1.20, and in the late phase it was 1.43, 1.38 and 0.97, respectively (each ANOVA p < 0.05). Conclusions: NHBD renal transplants were accompanied by a greater release of free radicals at reperfusion (NHBD > HBD > LD), which was associated with an increase in tissue injury markers at reperfusion. This was reflected in a slower return to stable renal function in NHBD compared to HBD and LD renal transplants.


Publication metadata

Author(s): Gok MA, Shenton BK, Pelsers M, Whitwood A, Mantle D, Cornell C, Peaston R, Rix DA, Jaques BC, Soomro NA, Manas DM, Talbot D

Publication type: Article

Publication status: Published

Journal: Journal of Urology

Year: 2006

Volume: 175

Issue: 2

Pages: 641-647

ISSN (print): 0022-5347

ISSN (electronic): 1527-3792

URL: http://dx.doi.org/10.1016/S0022-5347(05)00170-9

DOI: 10.1016/S0022-5347(05)00170-9


Altmetrics

Altmetrics provided by Altmetric


Share