Influence of Vitamin C on Antioxidant Capacity of In Vitro Perfused Porcine Kidneys.

acute kidney injury animal models antioxidant ascorbic acid kidney transplantation organ dysfunction oxidative stress porcine kidney perfusion model in vitro techniques primary graft dysfunction reperfusion injury vitamins

Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
01 Aug 2019
Historique:
received: 17 06 2019
revised: 25 07 2019
accepted: 29 07 2019
entrez: 4 8 2019
pubmed: 4 8 2019
medline: 29 1 2020
Statut: epublish

Résumé

Systemic and localized ischemia and reperfusion injury remain clinically relevant issues after organ transplantation and contribute to organ dysfunctions, among which acute kidney injury is one of the most common. An in vitro test-circuit for normothermic perfusion of porcine kidneys after warm ischemia was used to investigate the antioxidant properties of vitamin C during reperfusion. Vitamin C is known to enhance microcirculation, reduce endothelial permeability, prevent apoptosis, and reduce inflammatory reactions. Based on current evidence about the pleiotropic effects of vitamin C, we hypothesize that the antioxidant properties of vitamin C might provide organ-protection and improve the kidney graft function in this model of ischemia and reperfusion. 10 porcine kidneys from 5 Landrace pigs were perfused in vitro for 6 h. For each experiment, both kidneys of one animal were perfused simultaneously with a 1:1 mixture of autologous blood and modified Ringer's solution at 38 °C and 75 mmHg continuous perfusion pressure. One kidney was treated with a 500 mg bolus injection of vitamin C into the perfusate, followed by continuous infusion of 60 mg/h vitamin C. In the control test circuit, an equal volume of Ringer's solution was administered as a placebo. Perfusate samples were withdrawn at distinct points in time during 6 h of perfusion for blood gas analyses as well as measurement of serum chemistry, oxidative stress and antioxidant capacity. Hemodynamic parameters and urine excretion were monitored continuously. Histological samples were analyzed to detect tubular- and glomerular-injury. vitamin C administration to the perfusate significantly reduced oxidative stress (49.8 ± 16.2 vs. 118.6 ± 23.1 mV; Vitamin C treatment increased the antioxidant capacity of in vitro perfused kidney grafts, reduced oxidative stress, preserved red blood cells as oxygen carrier in the perfusate, but did not improve clinically relevant parameters like kidney function or attenuate kidney damage. Nevertheless, due to its antioxidative properties vitamin C might be a beneficial supplement to clinical kidney graft perfusion protocols.

Identifiants

pubmed: 31374900
pii: nu11081774
doi: 10.3390/nu11081774
pmc: PMC6722948
pii:
doi:

Substances chimiques

Antioxidants 0
Cytokines 0
Hemoglobins 0
Ascorbic Acid PQ6CK8PD0R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Christian Bleilevens (C)

Department of Anesthesiology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany. cbleilevens@ukaachen.de.

Benedict M Doorschodt (BM)

Institute for Laboratory Animal Science & Experimental Surgery, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Tamara Fechter (T)

Department of Anesthesiology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Tim Grzanna (T)

Department of Thoracic and Cardiovascular Surgery, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Alexander Theißen (A)

Department of Intensive Care Medicine and Intermediate Care, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Elisa A Liehn (EA)

Institute for Molecular Cardiovascular Research (IMCAR), Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.
Human Genetic Laboratory, University of Medicine and Pharmacy, RO-200000 Craiova, Romania.

Thomas Breuer (T)

Department of Intensive Care Medicine and Intermediate Care, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

René H Tolba (RH)

Institute for Laboratory Animal Science & Experimental Surgery, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Rolf Rossaint (R)

Department of Anesthesiology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Christian Stoppe (C)

Department of Intensive Care Medicine and Intermediate Care, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Peter Boor (P)

Institute of Pathology & Division of Nephrology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Aileen Hill (A)

Department of Anesthesiology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.
Department of Intensive Care Medicine and Intermediate Care, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

Gregor Fabry (G)

Department of Anesthesiology, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.
Department of Intensive Care Medicine and Intermediate Care, Medical Faculty RWTH Aachen University Hospital, D-52074 Aachen, Germany.

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Classifications MeSH