Literature DB >> 1580605

Kidney preservation ex vivo for transplantation.

J V Bonventre1, J M Weinberg.   

Abstract

Ischemic injury to the renal allograft, prior to implantation, is an important cause of delayed graft function. With improved understanding of the pathophysiological mechanisms involved, strategies have been devised to minimize ischemic injury during preservation ex vivo. It is clear that reducing the warm ischemic time, flushing the kidney with hypothermic solution containing cell-impermeant compounds, and maintaining the organ at low temperature ex vivo have increased the duration that the kidney can be preserved. The effectiveness of a number of other components of preservation solutions, as well as the relative merits of continuous perfusion of the organ ex vivo, is more controversial. In this chapter, we review the mechanistic features of ischemic acute renal failure and discuss various preservation strategies and their success in the context of these basic principles of ischemic pathophysiology.

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Year:  1992        PMID: 1580605     DOI: 10.1146/annurev.me.43.020192.002515

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  3 in total

Review 1.  The role of glycine in regulated cell death.

Authors:  Joel M Weinberg; Anja Bienholz; M A Venkatachalam
Journal:  Cell Mol Life Sci       Date:  2016-04-11       Impact factor: 9.261

2.  High Dose Meclizine Prevents Renal Ischemia-Reperfusion Injury in Healthy Male Mice.

Authors:  Gerard A Rongen
Journal:  EBioMedicine       Date:  2015-09-12       Impact factor: 8.143

3.  Effects of angiopeptin on transplant arteriosclerosis in the rat.

Authors:  M L Akyürek; A Wanders; M Aurivillius; E Larsson; K Funa; B C Fellström
Journal:  Transpl Int       Date:  1995       Impact factor: 3.782

  3 in total

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