Published online Dec 21, 2014. doi: 10.3748/wjg.v20.i47.17905
Revised: June 18, 2014
Accepted: July 15, 2014
Published online: December 21, 2014
Processing time: 259 Days and 19.3 Hours
AIM: To investigate the effects of terminal ileostomy on bacterial translocation (BT) and systemic inflammation after intestinal ischemia/reperfusion (I/R) injury in rats.
METHODS: Thirty-two rats were assigned to either the sham-operated group, I/R group, I/R + resection and anastomosis group, or the I/R + ileostomy group. The superior mesenteric artery was occluded for 60 min. After 4 h, tissue samples were collected for analysis. BT was assessed by bacteriologic cultures, intestinal permeability and serum levels of endotoxin; systemic inflammation was assessed by serum levels of tumor necrosis factor (TNF)-α, interleukin (IL)-6 and IL-10, as well as by the activity of myeloperoxidase (MPO) and by intestinal histopathology.
RESULTS: Intestinal I/R injury not only caused morphologic damage to ileal mucosa, but also induced BT, increased MPO activity and promoted the release of TNF-α, IL-6, and IL-10 in serum. BT and ileal mucosa injuries were significantly improved and levels of TNF-α and IL-6 in serum were decreased in the I/R + ileostomy group compared with the I/R + resection and anastomosis group.
CONCLUSION: Terminal ileostomy can prevent the detrimental effects of intestinal I/R injury on BT, intestinal tissue, and inflammation.
Core tip: Few studies have evaluated the occurrence of bacterial cecoileal reflux. We performed ileostomy to block the route of bacterial cecoileal reflux after intestinal ischemia/reperfusion injury. Compared with resection and anastomosis, ileostomy could improve the bacterial translocation, ileal mucosal injuries and systemic inflammation. The results provide a theoretic basis for the choice of ileostomy and resection/anastomosis in clinical practice.