PROTECTIVE ACTION OF THE GENISTEIN DERIVATIVE IN GASTRIC ULCER PREVENTION INDUCED BY ETHANOL IN RATS
Quan-Cheng Zhou, Gui-Hua Sheng, Xiang-Fei Chen, Na Liu, Chuan-Xing Feng,Guang-Yao Zhang, Xiao-Yu Yang, Hai-Liang Zhu
ABSTRACT
Aim: In the present study, a genistein derivative (GD) was firstly
synthesized and evaluated for antigastric ulcer activity in vivo and
investigated the possible mechanisms underlying the anti-ulcerogenic
effects of GD. Materials and methods: GD was synthesized through
genistein with phenylpiperazine, and was analyzed through 1H-NMR
and element analysis. GD was subjected to assess acute oral toxicity
study of animal model, and evaluate the protective effect of ethanolinduced gastric damage in rat model. Ulcer index value, NOx,
GSH/GSSG ratio, CAT, SOD, MPO activity, IL-6, IL-10 and PEG2
were also determined in the stomach tissues or blood serum. Results:
GD has no acute oral toxicity. GD (equivalent to 0.45, 4.5 and 45 mg/kg) dose-dependently
reduced the gastric ulcer index, significantly decreased the NOx, GSH/GSSG ratio, CAT
activity and IL-6, and increase SOD, MPO activity, IL-10, PEG2 and. Conclusion: GD
possesses an enhanced mucosal barrier defense activity. Their possible mechanism of action
was discussed and due to their many positive properties including antioxidant, antiinflammatory and gastroprotective activities might represent a cost effective alternative
sought for in the treatment of gastric ulcers. Based on the results, we suggest that GD has
potential to provide a therapeutic approach to ethanol mediated ulcer as an effective antiulcer agent.
Keywords: genistein, phenylpiperazine, synthesis, gastric ulcer, derivative, prevention.
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