Biliverdin Protects against Liver Ischemia Reperfusion Injury in Swine
Author(s) -
Barbara Andria,
Adele Bracco,
Chiara Attanasio,
Sigismondo Castaldo,
Maria Grazia Cerrito,
Santolo Cozzolino,
Daniele Di Napoli,
Roberto Giovani,
Antonio Mancini,
Antonino Musumeci,
E. Mezza,
Mario Nasti,
Vincenzo Scuderi,
Stefania Staibano,
Marialuisa Lavitrano,
Leo E. Otterbein,
Fulvio Calise
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0069972
Subject(s) - biliverdin , reperfusion injury , liver transplantation , bilirubin , transplantation , medicine , ischemia , pharmacology , pathology , animal model , hepatocyte , biology , heme , heme oxygenase , biochemistry , in vitro , enzyme
Ischemia reperfusion injury (IRI) in organ transplantation remains a serious and unsolved problem. Organs that undergo significant damage during IRI, function less well immediately after reperfusion and tend to have more problems at later times when rejection can occur. Biliverdin has emerged as an agent that potently suppress IRI in rodent models. Since the use of biliverdin is being developed as a potential therapeutic modality for humans, we tested the efficacy for its effects on IRI of the liver in swine, an accepted and relevant pre-clinical animal model. Administration of biliverdin resulted in rapid appearance of bilirubin in the serum and significantly suppressed IRI-induced liver dysfunction as measured by multiple parameters including urea and ammonia clearance, neutrophil infiltration and tissue histopathology including hepatocyte cell death. Taken together, our findings, in a large animal model, provide strong support for the continued evaluation of biliverdin as a potential therapeutic in the clinical setting of transplantation of the liver and perhaps other organs.
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