Post‐ischaemic restituted intestinal mucosa is more resistant to further ischaemia than normal mucosa in the pig

Abstract

Objective. Ischaemic preconditioning may protect the intestine from subsequent prolonged ischaemia. This study evaluates whether a much longer initial ischaemia, encountered clinically, may modify intestinal resistance to further ischaemia in a pig model. Material and methods. After cross‐clamping of the superior mesenteric artery for 1 h, the intestine was either reperfused for 8 h or a second cross‐clamping for 1 h was performed at 4 h of reperfusion. Based on microarray analysis of intestinal samples at 1, 4 and 8 h of reperfusion, mRNA of selected genes was measured with QRT‐PCR. Results. The first ischaemic period caused exfoliation of surface epithelial cells from the basement membrane comprising about 90 % of the villi tips, a marked increase in permeability and depletion of ATP. The second ischaemic challenge caused about 30 % less denudation of the basement membrane (p = 0.008), no increase in permeability (p = 0.008) and less depletion of ATP (p = 0.039). mRNAs for superoxide dismutase 2, heat shock proteins and signal transducer and activator of transcription 3, which may protect against ischaemia/reperfusion injury, were up‐regulated throughout the reperfusion period. mRNAs for matrix metalloproteinase 1, connexin 43 and peripheral myelin 22, which may be associated with cell migration or tight junctions, showed a particular up‐regulation at 4 h of reperfusion. Conclusion. One hour of initial ischaemia followed by 4 h of reperfusion is associated with increased intestinal resistance to further ischaemia. The differential regulation of genes identified in this study provides working hypotheses for mechanisms behind this observation.

• ATP
• histology
• intestine
• ischaemia
• microarray
• permeability
• reperfusion

Acknowledgements

We thank Karin Bakkelund, Oddveig Lyng and Borgny Ytterhus for excellent technical assistance. Financial support in the form of grants from the St. Olav University Hospital (No. 140110234630) and from the Sintef Unimed Research Fund are gratefully acknowledged.