Literature DB >> 3278416

Ablation of free radical-mediated reperfusion injury for the salvage of kidneys taken from non-heartbeating donors. A quantitative evaluation of the proportion of injury caused by reperfusion following periods of warm, cold, and combined warm and cold ischemia.

T Hoshino1, W R Maley, G B Bulkley, G M Williams.   

Abstract

Postischemic renal failure is a severe problem following cadaveric renal transplantation, especially if the kidney has been harvested from a non-heartbeating donor, and thereby subjected to periods of both warm and cold ischemia. It is well established that a substantial component of postischemic injury is produced by oxygen-derived free radicals generated from xanthine oxidase at reperfusion. However, the clinical potential of free radical ablative therapy is dependent upon the proportion of the total injury caused by this reperfusion mechanism, compared with the proportion resulting from ischemic injury per se. Therefore, we quantitatively evaluated these proportions in porcine kidneys subjected to various periods of warm (renal artery occlusion in situ), cold (harvest, cold preservation, and allotransplantation), and combined warm and cold ischemia. Experiments were paired, one kidney treated with either superoxide dismutase (SOD) or allopurinol for free radical ablation, the contralateral kidney serving as a control. Creatinine clearance (Ccr) was measured separately for each kidney 48 hr after reperfusion. After 1 and 2 hr of warm ischemia, Ccr dropped to 50% and 36% of normal, respectively. This was improved to 110% and 55% when SOD was given into the renal artery at reperfusion. Similarly, after 24 and 48 hr of cold ischemia, kidney function was significantly improved from 30% and 18% to 72% and 47% of normal, respectively, when allopurinol was added to the preservation solution. SOD used at harvest and again at reperfusion was particularly effective following combined warm and cold ischemia, in a situation mimicking the harvest of cadaver kidneys from a non-heartbeating donor. These findings suggest that the ablation of free radical-mediated reperfusion injury may improve posttransplant renal function sufficiently to allow expansion of the cadaveric donor pool to include non-heartbeating donors.

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Year:  1988        PMID: 3278416     DOI: 10.1097/00007890-198802000-00006

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  7 in total

Review 1.  Free radical ablation for the prevention of post-ischemic renal failure following renal transplantation.

Authors:  H J Schiller; K A Andreoni; G B Bulkley
Journal:  Klin Wochenschr       Date:  1991-12-15

2.  Comparison of superoxide dismutase, allopurinol, coenzyme Q10, and glutathione for the prevention of warm ischemic injury.

Authors:  W H Cho; D G Kim; N Murase; H J Mischinger; S Todo; T E Starzl
Journal:  Transplantation       Date:  1990-08       Impact factor: 4.939

3.  Hepatocyte growth factor-modified mesenchymal stem cells improve ischemia/reperfusion-induced acute lung injury in rats.

Authors:  S Chen; X Chen; X Wu; S Wei; W Han; J Lin; M Kang; L Chen
Journal:  Gene Ther       Date:  2016-08-24       Impact factor: 5.250

4.  Prevention of renal damage by alpha tocopherol in ischemia and reperfusion models of rats.

Authors:  Mustafa Cihat Avunduk; Talat Yurdakul; Esra Erdemli; Ayşe Yavuz
Journal:  Urol Res       Date:  2003-07-03

5.  Improved renal transplant preservation using a modified intracellular flush solution (PB-2). Characterization of mechanisms by renal clearance, high performance liquid chromatography, phosphorus-31 magnetic resonance spectroscopy, and electron microscopy studies.

Authors:  P N Bretan; N Baldwin; A Martinez; N Stowe; A Scarpa; K Easley; E Erturk; C Jackson; J Pestana; A C Novick
Journal:  Urol Res       Date:  1991

6.  The role of oxygen-derived free radicals and the effect of free radical scavengers on skeletal muscle ischemia/reperfusion injury.

Authors:  A Seyama
Journal:  Surg Today       Date:  1993       Impact factor: 2.549

7.  Cyclin-dependent kinase five mediates activation of lung xanthine oxidoreductase in response to hypoxia.

Authors:  Bo S Kim; Leonid Serebreni; Jonathan Fallica; Omar Hamdan; Lan Wang; Laura Johnston; Todd Kolb; Mahendra Damarla; Rachel Damico; Paul M Hassoun
Journal:  PLoS One       Date:  2015-04-01       Impact factor: 3.240

  7 in total

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