Literature DB >> 23010618

The autologous normothermic ex vivo perfused porcine liver-kidney model: improving the circuit's biochemical and acid-base environment.

Wen Yuan Chung1, Gianpiero Gravante, Dhya Al-Leswas, Ahmed Alzaraa, Roberto Sorge, Seok Ling Ong, Cristina Pollard, David M Lloyd, Matthew S Metcalfe, Ashley R Dennison.   

Abstract

BACKGROUND: The ex vivo porcine liver perfused model isolates the organ from extrinsic regulatory mechanisms, facilitating an improved understanding of the organ physiology and reaction to various conditions. We have assessed the influence of the addition of a porcine kidney to the circuit.
METHODS: Eight livers were harvested and perfused for 6 hours. In 5 additional experiments a kidney also was connected in parallel. Hourly arterial blood gases were collected to analyze glucose, acid base, and renal parameters. The primary end point was an evaluation of the influence of the kidney on glucose, pH, and electrolyte levels.
RESULTS: In the combined porcine liver-kidney circuit all the parameters significantly improved compared with the liver circuit alone. This was particularly evident for glucose values because normoglycemia was reached by the end of the perfusion, and for pH and electrolyte values that were maintained at initial levels.
CONCLUSIONS: The addition of a porcine kidney to the perfusion circuit improves the biochemical milieu. This might produce more consistent and reliable results, particularly during studies requiring a steady-state environment.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23010618     DOI: 10.1016/j.amjsurg.2011.11.016

Source DB:  PubMed          Journal:  Am J Surg        ISSN: 0002-9610            Impact factor:   2.565


  6 in total

1.  Addition of a kidney to the normothermic ex vivo perfused porcine liver model does not increase cytokine response.

Authors:  Wen Yuan Chung; Gianpiero Gravante; Dhya Al-Leswas; Ahmed Alzaraa; Roberto Sorge; Seok Ling Ong; Cristina Pollard; David M Lloyd; Matthew S Metcalfe; Ashley R Dennison
Journal:  J Artif Organs       Date:  2012-04-04       Impact factor: 1.731

2.  Steps for the autologous ex vivo perfused porcine liver-kidney experiment.

Authors:  Wen Yuan Chung; Amar M Eltweri; John Isherwood; Jonathan Haqq; Seok Ling Ong; Gianpiero Gravante; David M Lloyd; Matthew S Metcalfe; Ashley R Dennison
Journal:  J Vis Exp       Date:  2013-12-18       Impact factor: 1.355

3.  Contrast-enhanced ultrasound detects perfusion defects in an ex vivo porcine liver model: a useful tool for the study of hepatic reperfusion.

Authors:  Ahmed Alzaraa; Dhya Al-Leswas; Wen Yuan Chung; Gianpiero Gravante; Morgan Bruno; Kevin West; Ashley Dennison; David Lloyd
Journal:  J Artif Organs       Date:  2013-06-29       Impact factor: 1.731

4.  The "kidney-liver" multiorgan ex vivo perfused model improves the circuit's biochemical milieu during perfusion compared to the "liver-kidney" counterpart.

Authors:  Wen Yuan Chung; Gianpiero Gravante; Amar Eltweri; Roberto Sorge; Seok Ling Ong; Cristina Pollard; Mathew Metcalfe; Ashley Dennison
Journal:  J Artif Organs       Date:  2015-01-04       Impact factor: 1.731

5.  History, ethics, advantages and limitations of experimental models for hepatic ablation.

Authors:  Seok Ling Ong; Gianpiero Gravante; Matthew S Metcalfe; Ashley R Dennison
Journal:  World J Gastroenterol       Date:  2013-01-14       Impact factor: 5.742

Review 6.  Normothermic Ex-vivo Liver Perfusion and the Clinical Implications for Liver Transplantation.

Authors:  Clifford Akateh; Eliza W Beal; Bryan A Whitson; Sylvester M Black
Journal:  J Clin Transl Hepatol       Date:  2018-05-04
  6 in total

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