To determine the role of endothelins (ET) on experimental colitis, followin
g intracolonic trinitrobenzene sulfonic acid administration, rats were give
n orally either bosentan (BS), a nonselective ET receptor antagonist (100 m
g/kg in 5% arabic gum), or arabic gum by gavage for 2 or 14 days. Macroscop
ic damage scores obtained in the vehicle (1.4 +/- 0.4), acute (4.8 +/- 0.6)
and chronic (3.8 +/- 0.3) colitis groups were significantly higher than in
the control group (0). BS treatment reduced the scores in both acute (3 +/
- 0.5) and chronic (2.3 +/- 0.5) colitis groups. Myeloperoxidase (MPO) acti
vities of colonic tissues were elevated in acute and chronic colitis groups
(325.1 +/- 44.9 and 431.8 +/- 54.6 U/g wet weight) as compared with the co
ntrol group (73.6 +/- 11 U/g wet weight). Plasma protein oxidation levels w
ere found to be significantly increased in the chronic colitis group (1,158
.1 +/- 63.4 nmol/ml) compared with the control, ethanol and acute colitis g
roups (274.3 +/- 23.1, 490 +/- 52.2 and 422.2 +/- 50.5 nmol/ml). BS treatme
nt significantly reduced both the protein oxidation level (375.5 +/- 46.9 n
mol/ml) and MPO activity (167.5 +/- 35.8 U/g wet weight). The results of th
e present study suggest the involvement of ETs in the pathogenesis of colon
ic injury in this animal model of colitis.