4.6 Article

Effect of cisapride on intestinal bacterial and endotoxin translocation in cirrhosis

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 9, Issue 3, Pages 534-538

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v9.i3.534

Keywords

-

Ask authors/readers for more resources

AIM: To investigate the effects of cisapride on intestinal bacterial overgrowth (IBO), bacterial and endotoxin translocation, intestinal transit and permeability in cirrhotic rats. METHODS: All animals were assessed with variables including bacterial and endotoxin translocation, intestinal bacterial overgrowth, intestinal transit and permeability. Bacterial translocation (BT) was assessed by bacterial culture of MLN, liver and spleen, IBO by a jejunal bacterial count of the specific organism, intestinal permeability by determination of the 24-hour urinary Tc-99m-DTPA excretion and intestinal transit by measurement of the distribution of Cr-51 in the intestine. RESULTS: Bacterial translocation (BT) and IBO was found in 48 % and 80 % cirrhotic rats respectively and none in control rats. Urinary excretion of Tc-99m-DTPA in cirrhotic rats with BT (22.2 +/- 7.8) was greater than these without BT (10.5 +/- 2.9). Intestinal transit (geometric center ratio) was significantly delayed in cirrhotic rats (0.31 +/- 0.06) and further more delayed in cirrhotic rats with BT (0.24 +/- 0.06) than these without BT (0.38 +/- 0.11). Cirrhotic rats with IBO had significantly higher rates of intestinal bacterial and endotoxin translocation, slower intestinal transit time and higher intestinal permeability than those without IBO. It was also found that BT was closely associated with IBO and the injury of intestinal barrier. Compared with the placebo group, cisapride-treated rats had lower rates of bacterial/endotoxin translocation and IBO, which was closely associated with increased intestinal transit and improved intestinal permeability by cisapride. CONCLUSION: These results indicate that endotoxin and bacterial translocation in cirrhotic rats may be attributed to IBO and increased intestinal permeability. Cisapride that accelerates intestinal transit and improve intestinal permeability might be helpful in preventing intestinal bacterial and endotoxin translocation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available