AI Article Synopsis

  • Intestinal preservation for transplantation often involves long periods of ischemia that can cause structural damage due to lack of blood and oxygen supply.
  • This study tested a method of delivering intraluminal oxygen during warm ischemia in a pig model to see if it could prevent ischemic damage.
  • Results showed that the pigs receiving intraluminal oxygen had better mucosal integrity and overall viability compared to the control group, suggesting it could enhance methods for preserving the intestine for transplantation.

Article Abstract

Intestinal preservation for transplantation is accompanied by hypoperfusion with long periods of ischemia with total blood cessation and absolute withdrawal of oxygen leading to structural damage. The application of intraluminal oxygen has been successfully tested in small-animal series during storage and transport of the organ but have been so far clinically unrelatable. In this study, we tested whether a simple and clinically approachable method of intraluminal oxygen application could prevent ischemic damage in a large animal model, during warm ischemia time. We utilised a local no-flow ischemia model of the small intestine in pigs. A low-flow and high-pressure intraluminal oxygen deliverance system was applied in 6 pigs and 6 pigs served as a control group. Mucosal histopathology, hypoxia and barrier markers were evaluated after two hours of no-flow conditions, in both treatment and sham groups, and in healthy tissue. Macro- and microscopically, the luminal oxygen delivered treatment group showed preserved small bowel's appearance, viability, and mucosal integrity. A gradual deterioration of histopathology and barrier markers and increase in hypoxia-inducible factor 1-α expression towards the sites most distant from the oxygen application was observed. Intraluminal low-flow, high oxygen delivery can preserve the intestinal mucosa during total ischemia of the small intestine. This finding can be incorporated in methods to overcome small bowel ischemia and improve intestinal preservation for transplantation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11178904PMC
http://dx.doi.org/10.1038/s41598-024-64660-xDOI Listing

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