Orally administered RDP58 reduces the severity of dextran sodium sulphate induced colitis.

Abstract

Oral administration of the novel anti-inflammatory peptide RDP58 markedly reduced the severity of dextran sulphate sodium (DSS) colitis as determined by clinical and quantitative histological criteria. The architecture of the colonic epithelium in DSS treated mice receiving RDP58 remained relatively normal compared with that of control DSS treated animals. 5-Bromo-2'-deoxyuridine (BrdU) labelling studies showed a pronounced inhibition of colonic epithelial cell proliferation during DSS treatment, which was partially reversed by RDP58 therapy. Remarkably, RDP58 almost completely prevented colonic epithelial cell death induced by DSS treatment. RDP58 therapy also inhibited the accumulation of neutrophils in the colon of DSS treated mice and effectively down regulated tumour necrosis factor (TNF) expression. Preservation of the intestinal mucosa by RDP58 may thus derive from its influence on TNF expression as well as additional anti-inflammatory properties. These findings indicate that RDP58 represents a new, orally available agent potentially useful in the treatment of inflammatory bowel disease.

• Authors: R Boismenu, Y Chen, K Chou, A El-Sheikh, R Buelow
• Journal: Annals of the rheumatic diseases (Ann Rheum Dis) Vol. 61 Suppl 2 Pg. ii19-24 (Nov 2002) ISSN: 0003-4967 [Print] England
• PMID: 12379615 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Anti-Inflammatory Agents
• Peptides
• Tumor Necrosis Factor-alpha
• allotrap
• Dextran Sulfate

Topics

• Acute Disease
• Administration, Oral
• Animals
• Anti-Inflammatory Agents (therapeutic use)
• Apoptosis (drug effects)
• Cell Division (drug effects)
• Colitis (chemically induced, pathology, prevention & control)
• Dextran Sulfate
• Epithelial Cells (drug effects, pathology)
• Female
• Intestinal Mucosa (drug effects, pathology)
• Mice
• Mice, Inbred C57BL
• Neutrophil Infiltration (drug effects)
• Peptides (therapeutic use)
• Tumor Necrosis Factor-alpha (biosynthesis)