Calpain inhibitor I reduces colon injury caused by dinitrobenzene sulphonic acid in the rat
Open Access
- 1 April 2001
- Vol. 48 (4) , 478-488
- https://doi.org/10.1136/gut.48.4.478
Abstract
BACKGROUND AND AIMS Inflammatory bowel disease is characterised by oxidative and nitrosative stress, leucocyte infiltration, upregulation of expression of intercellular adhesion molecule 1 (ICAM-1), and upregulation of P-selectin in the colon. The aim of the present study was to examine the effects of calpain inhibitor I in rats subjected to experimental colitis. METHODS Colitis was induced in rats by intracolonic instillation of dinitrobenzene sulphonic acid (DNBS). RESULTS Rats experienced haemorrhagic diarrhoea and weight loss. Four days after administration of DNAB, the mucosa of the colon exhibited large areas of necrosis. Neutrophil infiltration (determined by histology as well as by an increase in myeloperoxidase activity in the mucosa) was associated with upregulation of ICAM-1 and P-selectin as well as high tissue levels of malondialdehyde. Immunohistochemistry for nitrotyrosine and poly (ADP-ribose) polymerase (PARP) showed intense staining in the inflamed colon. Staining of sections of colon obtained from DNBS treated rats with an anti-cyclooxygenase 2 antibody showed diffuse staining of the inflamed tissue. Furthermore, expression of inducible nitric oxide synthase was found mainly in macrophages located within the inflamed colon of DNBS treated rats. Calpain inhibitor I (5 mg/kg daily intraperitoneally) significantly reduced the degree of haemorrhagic diarrhoea and weight loss caused by administration of DNBS. Calpain inhibitor I also caused a substantial reduction in (i) degree of colon injury, (ii) rise in myeloperoxidase activity (mucosa), (iii) increase in tissue levels of malondialdehyde, (iv) increase in staining (immunohistochemistry) for nitrotyrosine and PARP, as well as (v) upregulation of ICAM-1 and P-selectin caused by DNBS in the colon. CONCLUSION Calpain inhibitor I reduces the degree of colitis caused by DNBS. We propose that calpain inhibitor I may be useful in the treatment of inflammatory bowel disease.Keywords
This publication has 77 references indexed in Scilit:
- Myeloperoxidase activity as a quantitative assessment of neutrophil infiltration into ischemie myocardiumPublished by Elsevier ,2002
- Six-Hour Window of Opportunity for Calpain Inhibition in Focal Cerebral Ischemia in RatsStroke, 1998
- RETRACTED: Peroxynitrite‐mediated DNA strand breakage activates poly (ADP‐ribose) synthetase and causes cellular energy depletion in carrageenan‐induced pleurisyImmunology, 1998
- Increased oxidative stress and decreased antioxidant defenses in mucosa of inflammatory bowel diseaseDigestive Diseases and Sciences, 1996
- Proteolytic processing of nuclear factor κB by calpain in vitroFEBS Letters, 1996
- Serine and Cysteine Proteinase Inhibitors Prevent Nitric Oxide Production by Activated Macrophages by Interfering with Transcription of the Inducible NO Synthase GeneBiochemical and Biophysical Research Communications, 1995
- Oxidative DNA damage induced by simultaneous generation of nitric oxide and superoxideFEBS Letters, 1995
- Effects of zileuton, a new 5-lipoxygenase inhibitor, in experimentally induced colitis in ratsInflammation Research, 1993
- Protective Effect of the Protease Inhibitor Leupeptin Against Myocardial StunningJournal of Cardiovascular Pharmacology, 1993
- Calcium-activated neutral protease inhibitor(E-64c) and reperfusion for experimental myocardial infarction.Japanese Heart Journal, 1989