Toxicology mechanisms and methods · 2014
Protective effects of escin against indomethacin-induced gastric ulcer in mice.
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Wang Tian, Zhao Shanshan, Wang Yucun, Yang Yujiao, Yao Le, Chu Liuxiang, Du Hanhan, Fu Fenghua
Аннотация
Escin, a natural mixture of triterpenoid saponin isolated from the seed of the horse chestnut, is reported to have a potent antiulcer activity against ethanol-induced gastric mucosal lesions. This study investigated the possible mechanisms underlying the gastroprotective effect of escin against indomethacin-induced gastric ulcer in mice. Gastric ulceration was induced by a single intragastric administration of indomethacin (18 mg/kg). The mice underwent intragastric treatment with escin at doses of 0.45, 0.9 or 1.8 mg/kg. Gastric lesion was estimated morphometrically and histopathologically 6 h after the indomethacin administration. The antioxidative parameters in gastric mucosa were measured. Moreover, the activity of myeloperoxidase and the contents of TNF-α, P-selectin and VCAM-1 in gastric tissues were determined. The results showed that escin protected gastric tissues against indomethacin-induced gastropathy as demonstrated from a reduction in the ulcer index and an attenuation of histopathologic changes. Escin caused significant reductions of the contents of malondialdehyde, TNF-α, P-selectin, VCAM-1 and myeloperoxidase activity. The altered activities of superoxide dismutase, catalase and glutathione peroxidase in the stomach tissues were also ameliorated by escin treatment. The present study demonstrated that escin had a protective effect against indomethacin-induced gastric ulcer in mice, not only by virtue of its antioxidant potential, but also due to its anti-inflammatory effect.
Предметные рубрики MeSH
AnimalsAnti-Inflammatory Agents, Non-SteroidalAnti-Ulcer AgentsAntioxidantsDose-Response Relationship, DrugEscinGastric MucosaH(+)-K(+)-Exchanging ATPaseIndomethacinLipid PeroxidationMiceOxidoreductasesP-SelectinProtective AgentsRandom AllocationSeverity of Illness IndexStomachStomach UlcerTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1