Reduced ischemia-reoxygenation injury in rat intestine after luminal preservation with a tailored solution

• Published in: Transplantation Vol. 90; no. 6; p. 622
• Main Authors: Roskott, Anne Margot, Nieuwenhuijs, Vincent B, Leuvenink, Henri G D, Dijkstra, Gerard, Ottens, Petra, de Jager, Marina H, Gonalves Dias Pereira, Patricia, Fidler, Vaclav, Groothuis, Geny M M, Ploeg, Rutger J, de Graaf, Inge A M
• Format: Journal Article
• Language: English
• Published: United States 27.09.2010
• Subjects: Adenosine; Allopurinol; Animals; Cell Survival; Gene Expression Regulation; Glutathione; Ice; Insulin; Intestinal Mucosa - cytology; Intestinal Mucosa - pathology; Intestines - cytology; Intestines - pathology; Intestines - physiopathology; Ischemia - prevention & control; Microvilli - pathology; Microvilli - physiology; Organ Preservation - methods; Organ Preservation Solutions; Raffinose; Rats; RNA, Messenger - genetics; RNA, Messenger - isolation & purification
• ISSN: 1534-6080
• DOI: 10.1097/TP.0b013e3181ebf796

The intestine is extremely sensitive to ischemic preservation and reoxygenation injury. Current vascular perfusion and cold storage with University of Wisconsin (UW) solution neglect the intestinal lumen and the ongoing mucosal metabolism during hypothermia. This study was designed to test the effects of luminal preservation with an alternative preservation solution in addition to the common vascular flush with UW solution on graft viability after preservation and ex vivo reoxygenation. Rat intestine was preserved on ice for 6 hr in UW solution or Williams Medium E with additional buffering, impermeants, and a colloid (WMEplus) after being stapled or after flushing and filling the lumen with the respective preservation solution. Tissue slices were prepared from fresh and preserved intestines and were incubated with oxygen for 6 hr at 37°C to assess the viability after reoxygenation. Directly after preservation, histologic damage was mild and unaffected by preservation strategy. Contrary to luminal preservation, closed preservation resulted in significantly decreased ATP levels compared with control. Reoxygenation aggravated damage and revealed differences between the strategies. Luminal preservation better maintained the ATP levels and histologic integrity (vs. closed preservation) for both solutions. Histomorphologic integrity was superior after preservation with WMEplus (vs. UW solution). Expression of stress responsive genes was least up-regulated in the slices from tissue preserved luminally with WMEplus. In conclusion, preservation and reoxygenation injury can be attenuated by luminal preservation with WMEplus.