Meloxicam is a new non-steroidal anti-inflammatory drug, that possesses a s
elective inhibition of the inducible isoform of cyclooxygenase enzyme (COX-
2) relative to the constitutive one, COX-1. Oxidative stress has been docum
ented to be involved in the aetiology of many pathological conditions. The
present study aims to further explore the relationship between free radical
generation and the inflammatory process, and extends more to investigate t
he effect of meloxicam on the oxidant status in experimentally induced arth
ritis, namely, Freund's adjuvant-induced arthritis in rats. Results of the
present investigation revealed that animals inoculated with Freund's comple
te adjuvant showed a biphasic response regarding changes in the right hind
paw oedema volume. During the chronic phase of the disease, arthritic anima
ls showed an elevated plasma level of lipid peroxides, enhanced blood gluta
thione peroxidase activity, with depletion of plasma total thiols and album
in; while no significant effects have been observed on erythrocytic superox
ide dismutase activity and plasma total proteins content, as compared to no
rmal untreated rats. Long-term administration of meloxicam, at two dose lev
els, produced significant antioedemetous effect and succeeded in modulating
the altered parameters affected during arthritis. The selected dose regime
ns of meloxicam did not show any apparent lesions in the gastric mucose. Th
e results of the present investigation lend further support to the reported
observations concerning selective COX-2 inhibitors. The modulatory influen
ce of meloxicam on the oxidant status, particularly on lipid peroxidation a
nd thiols might be a relevant effect accounting for its anti-inflammatory p
roperties. (C) 1999 Academic Press.