Ischemia-Reperfusion Injuries Assessment during Pancreas Preservation.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
13 May 2021
Historique:
received: 13 03 2021
revised: 25 04 2021
accepted: 10 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 11 6 2021
Statut: epublish

Résumé

Maintaining organ viability between donation and transplantation is of critical importance for optimal graft function and survival. To date in pancreas transplantation, static cold storage (SCS) is the most widely practiced method of organ preservation. The first experiments in ex vivo perfusion of the pancreas were performed at the beginning of the 20th century. These perfusions led to organ oedema, hemorrhage, and venous congestion after revascularization. Despite these early hurdles, a number of factors now favor the use of perfusion during preservation: the encouraging results of HMP in kidney transplantation, the development of new perfusion solutions, and the development of organ perfusion machines for the lung, heart, kidneys and liver. This has led to a resurgence of research in machine perfusion for whole organ pancreas preservation. This review highlights the ischemia-reperfusion injuries assessment during ex vivo pancreas perfusion, both for assessment in pre-clinical experimental models as well for future use in the clinic. We evaluated perfusion dynamics, oedema assessment, especially by impedance analysis and MRI, whole organ oxygen consumption, tissue oxygen tension, metabolite concentrations in tissue and perfusate, mitochondrial respiration, cell death, especially by histology, total cell free DNA, caspase activation, and exocrine and endocrine assessment.

Identifiants

pubmed: 34068301
pii: ijms22105172
doi: 10.3390/ijms22105172
pmc: PMC8153272
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Thomas Prudhomme (T)

Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, 44000 Nantes, France.
Centre de Recherche en Transplantation et Immunologie (CRTI) UMR1064, INSERM, Université de Nantes, 44000 Nantes, France.

John F Mulvey (JF)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Liam A J Young (LAJ)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.
Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Radcliffe Department of Medicine, University of Oxford, Oxford OX3 9DU, UK.

Benoit Mesnard (B)

Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, 44000 Nantes, France.
Centre de Recherche en Transplantation et Immunologie (CRTI) UMR1064, INSERM, Université de Nantes, 44000 Nantes, France.

Maria Letizia Lo Faro (ML)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Ann Etohan Ogbemudia (AE)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Fungai Dengu (F)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Peter J Friend (PJ)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Rutger Ploeg (R)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

James P Hunter (JP)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Julien Branchereau (J)

Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, 44000 Nantes, France.
Centre de Recherche en Transplantation et Immunologie (CRTI) UMR1064, INSERM, Université de Nantes, 44000 Nantes, France.
Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

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