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Nephrol Dial Transplant (2001) 16: 1262-1266
© 2001 European Renal Association-European Dialysis and Transplant Association


Technical Note

An experimental sclerosing encapsulating peritonitis model in mice

Yasuo Ishii1, Tokihiko Sawada1,, Akira Shimizu2, Tamotsu Tojimbara1, Ichiro Nakajima1, Shohei Fuchinoue1 and Satoshi Teraoka1

1 Tokyo Women's Medical University, Kidney Center, Department of Surgery and 2 Nippon Medical School, Department of Pathology, Tokyo, Japan

Abstract

Background. Sclerosing encapsulating peritonitis (SEP) is a life-threatening complication of continuous ambulatory peritoneal dialysis. To elucidate the mechanism and develop treatments for this condition, an experimental SEP model in mice was constructed.

Methods. C57BL/6 mice were administered 0.3 ml of 0.1% chlorhexidine gluconate and 15% ethanol dissolved in saline, intraperitoneally, on a daily basis for 56 days (group 1, n=15). A control group of C57BL/6 mice were administered 0.3 ml of phosphate-buffered saline only in the same manner (group 2, n=15). The mice were sacrificed on days 3, 7, 21, 56 and were prepared for histological analysis.

Results. In group 1, all mice had developed macroscopic evidence of SEP 56 days after the injection. Microscopically we observed peritoneal fibrosis and an increase in infiltrates of mononuclear cells over time. The peritoneal fibrosis reached the chronic inflammatory stage by 56 days after the injection.

Conclusion. We have developed a convenient experimental model of SEP in mice, which may be useful in elucidating the pathogenesis of SEP and in establishing possible treatments.

Keywords: chlorhexidine gluconate; ethanol; murine model; peritoneal dialysis; sclerosing encapsulating peritonitis

Notes

Correspondence and offprint requests to: Tokihiko Sawada, Tokyo Women's Medical University, Kidney Center, Department of Surgery, 8-1 Kawata-cho, Shinjuku-ku, Tokyo 162-8666, Japan.


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