A gastroprotective effect occurs when α(2) receptors are innervated. The dextro isomer of
medetomidine,
dexmedetomidine, is a highly selective α(2)-adrenoreceptor agonist. The aim of this study was to investigate whether
dexmedetomidine has an antiulcerative effect and to show whether the antiulcer mechanism of
dexmedetomidine is linked with
oxidant/
antioxidant parameters. The antiulcerative effect of
dexmedetomidine was studied in an
indomethacin-induced
ulcer model, and some
oxidant/
antioxidant parameters were measured in these gastric tissues. Whereas the average ulcerous areas for the groups that received 10, 25, 50, and 100 μg/kg
dexmedetomidine doses were 29 ± 4.2, 8 ± 2.1, 0 ± 0 and 0 ± 0 mm(2), respectively, the ulcerous area was 52.1 ± 4.5 mm(2) in the
indomethacin control group and 0.5 ± 0.2 mm(2) in the
famotidine group. In conclusion, the α(2)-adrenoreceptor agonist
dexmedetomidine showed a significant antiulcerative effect in rat gastric tissue at all doses. This antiulcerative effect is stronger with increasing dosage; at the 50 and 100 μg/kg doses, no ulcerous areas were observed. In light of these results, we conclude that there is a correlation between antiulcer mechanisms and α(2)-receptor activation. In rats given
dexmedetomidine, all of the investigated
antioxidant parameters increased, except for
catalase (CAT). Conversely, aside from
myeloperoxidase (MPO), all
oxidant parameters decreased. Therefore,
oxidant/
antioxidant parameters play a role in the antiulcer mechanism of
dexmedetomidine.