In vivo antioxidant and antiulcer activity of Parkia speciosa ethanolic leaf extract against ethanol-induced gastric ulcer in rats

PLoS One. 2013 May 28;8(5):e64751. doi: 10.1371/journal.pone.0064751. Print 2013.

Abstract

Background: The current study was carried out to examine the gastroprotective effects of Parkia speciosa against ethanol-induced gastric mucosa injury in rats.

Methodology/principal findings: Sprague Dawley rats were separated into 7 groups. Groups 1-2 were orally challenged with carboxymethylcellulose (CMC); group 3 received 20 mg/kg omeprazole and groups 4-7 received 50, 100, 200 and 400 mg/kg of ethanolic leaf extract, respectively. After 1 h, CMC or absolute ethanol was given orally to groups 2-7. The rats were sacrificed after 1 h. Then, the injuries to the gastric mucosa were estimated through assessment of the gastric wall mucus, the gross appearance of ulcer areas, histology, immunohistochemistry and enzymatic assays. Group 2 exhibited significant mucosal injuries, with reduced gastric wall mucus and severe damage to the gastric mucosa, whereas reductions in mucosal injury were observed for groups 4-7. Groups 3-7 demonstrated a reversal in the decrease in Periodic acid-Schiff (PAS) staining induced by ethanol. No symptoms of toxicity or death were observed during the acute toxicity tests.

Conclusion: Treatment with the extract led to the upregulation of heat-shock protein 70 (HSP70) and the downregulation of the pro-apoptotic protein BAX. Significant increases in the levels of the antioxidant defense enzymes glutathione (GSH) and superoxide dismutase (SOD) in the gastric mucosal homogenate were observed, whereas that of a lipid peroxidation marker (MDA) was significantly decreased. Significance was defined as p<0.05 compared to the ulcer control group (Group 2).

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Anti-Ulcer Agents / adverse effects
  • Anti-Ulcer Agents / pharmacology
  • Anti-Ulcer Agents / therapeutic use*
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use*
  • Ethanol
  • Fabaceae / chemistry*
  • Female
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / metabolism
  • Gastric Mucosa / pathology
  • Glutathione / metabolism
  • HSP70 Heat-Shock Proteins / metabolism
  • Hydrogen-Ion Concentration / drug effects
  • Immunohistochemistry
  • Male
  • Malondialdehyde / metabolism
  • Mucus / metabolism
  • Periodic Acid-Schiff Reaction
  • Plant Extracts / adverse effects
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use*
  • Plant Leaves / chemistry*
  • Rats
  • Rats, Sprague-Dawley
  • Stomach Ulcer / drug therapy*
  • Stomach Ulcer / enzymology
  • Stomach Ulcer / pathology
  • Superoxide Dismutase / metabolism
  • Toxicity Tests, Acute
  • bcl-2-Associated X Protein / metabolism

Substances

  • Anti-Ulcer Agents
  • Antioxidants
  • HSP70 Heat-Shock Proteins
  • Plant Extracts
  • bcl-2-Associated X Protein
  • Ethanol
  • Malondialdehyde
  • Superoxide Dismutase
  • Glutathione

Grants and funding

The authors express gratitude to the University of Malaya for the financial support of UM/MOHE High Impact Research Grant (HIR Grant No. F000009-21001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.