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A natural tetrahydropyrimidine, ectoine, ameliorates ischemia reperfusion injury after intestinal transplantation in rats

  • Thomas Pech
  • , Ichiro Ohsawa
  • , Michael Praktiknjo
  • , Marcus Overhaus
  • , Sven Wehner
  • , Martin von Websky
  • , Kareem Abu-Elmagd
  • , Gerhild van Echten-Deckert
  • , Joerg C. Kalff
  • , Nico Schaefer
  • University of Bonn
  • Mie University
  • Department of Neurology, Stroke Institute, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background/Aims: Ischemia reperfusion (I/R) injury after small bowel transplantation leads to inflammatory reactions and loss of structural integrity with subsequent graft contractile dysfunction in the early postoperative phase. The natural tetrahydropyrimidine ectoine (1-,4-,5-,6-tetrahydro-2-methyl-4- pyrimidine carboxylic acid; THP) protects the ileal mucosa and muscularis against effects of I/R injury in an experimental model of isolated graft reperfusion. The effects of THP treatment were evaluated in an established experimental intestinal transplant model. Methods: Isogenic, orthotopic small bowel transplantation was performed in Lewis rats (6 h cold ischemia time). Perioperative THP treatment (intraluminal/intravascular) groups were compared to vehicle-treated animals (after 3 and 24 h) and non-transplanted controls (n = 5/group). Park's score defined the effects of I/R injury. The infiltration of neutrophils, monocytes and macrophages, mRNA expression of IL-6 and TNF-α, serum levels of IL-6 and NO and smooth muscle contractility were evaluated. Results: Improved graft outcome after intraluminal and intravascular THP treatment was defined by considerably ameliorated neutrophil infiltration and less histological signs of I/R injury (p ≤ 0.05). In the presence of THP, mRNA expression of IL-6 and TNF-α and IL-6 and NO serum levels were reduced and smooth muscle function was improved. Conclusion: THP treatment offers protection against the effects of I/R injury in intestinal transplantation in vivo, however, only as supplementary treatment option. Copyright © 2012 S. Karger AG, Basel.
Original languageEnglish
Pages (from-to)102-110
JournalPathobiology
Volume80
Issue number2
DOIs
Publication statusPublished - Nov 2012
Externally publishedYes

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