Abstract

Introduction: Gastric ulcer (GU) is the most common gastrointestinal tract disorder, representing about 20% of peptic ulcer due to an imbalance between gastric defense mechanisms and aggressive factors, mainly Helicobacter pylori and non-steroidal anti-infl ammatory drugs (NSAIDs). The study aims to evaluate trimetazidine’s protective eff ect on histopathology, GU severity, infl ammatory and oxidative stress markers (TNF- alpha, MPO and MDA) in rate model of indomethacin induced GU. Method: Total 30 healthy male albino rats were divided into fi ve groups each of ten (N=10). Group A: Given indomethacin vehicles (normal saline 0.9% and tween 80) orally via gavage tube and serve as control positive group. Group B: Induced ulcer by Indomethacin 60 mg/kg orally via oral gavage serve as control negative. Group C: Pretreated with trimetazidine 50 mg/ kg orally by gavage tube 1-hour before administering indomethacin 60 mg/kg. At the end of study histological examination, anti-infl ammatory and antioxidant markers were evaluated. Results: TMZ 50 mg/kg pretreated groups show a signifi cant (p 0.01) reduction in GU severity score and histopathology damage score in comparison with the indomethacin ulcerated group. Moreover, pretreated groups TMZ 50 mg/kg showed a signifi cant reduction in infl ammatory markers (TNF-alpha and MPO) and oxidative stress marker (MDA) in comparison with the induction group, similar to the results of the reference drug. Conclusion: TMZ dihydrochloride has similar effi cacy as standard omeprazole drug by a decrease in oxidative stress status manifested by a reduction in lipid peroxidation indicator marker and a reduction in pro-infl ammatory cytokine level and leukocyte recruitment indicator marker and fi nally, macroscopic and microscopic evaluation show a reduction GU severity.

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