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Protective effects of escin against indomethacin-induced gastric ulcer in mice.

Authors :
Wang, Tian
Zhao, Shanshan
Wang, Yucun
Yang, Yujiao
Yao, Le
Chu, Liuxiang
Du, Hanhan
Fu, Fenghua
Source :
Toxicology Mechanisms & Methods. Dec2014, Vol. 24 Issue 8, p560-566. 7p. 1 Color Photograph, 5 Graphs.
Publication Year :
2014

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15376516
Volume :
24
Issue :
8
Database :
Academic Search Index
Journal :
Toxicology Mechanisms & Methods
Publication Type :
Academic Journal
Accession number :
99076150
Full Text :
https://doi.org/10.3109/15376516.2014.951815