Biochanin a gastroprotective effects in ethanol-induced gastric mucosal ulceration in rats

PLoS One. 2015 Mar 26;10(3):e0121529. doi: 10.1371/journal.pone.0121529. eCollection 2015.

Abstract

Background: Biochanin A notable bioactive compound which is found in so many traditional medicinal plant. In vivo study was conducted to assess the protective effect of biochanin A on the gastric wall of Spraguedawley rats` stomachs.

Methodology: The experimental set included different animal groups. Specifically, four groups with gastric mucosal lesions were receiving either a) Ulcer control group treated with absolute ethanol (5 ml/kg), b) 20 mg/kg of omeprazole as reference group, c) 25 of biochanin A, d) 50 mg/kg of biochanin A. Histopathological sectioning followed by immunohistochemistry staining were undertaken to evaluate the influence of the different treatments on gastric wall mucosal layer. The gastric secretions were collected in the form of homogenate and exposed to superoxide dismutase (SOD) and nitric oxide enzyme (NO) and the level of malondialdehyde (MDA) and protein content were measured. Ulceration and patchy haemorrhage were clearly observed by light microscopy. The morphology of the gastric wall as confirmed by immunohistochemistry and fluorescent microscopic observations, exhibited sever deformity with notable thickness, oedematous and complete loss of the mucosal coverage however the biochanin-pretreated animals, similar to the omeprazole-pretreated animals, showed less damage compared to the ulcer control group. Moreover, up-regulation of Hsp70 protein and down-regulation of Bax protein were detected in the biochanin A pre-treated groups and the gastric glandular mucosa was positively stained with Periodic Acid Schiff (PAS) staining and the Leucocytes infiltration was commonly seen. Biochanin A displayed a great increase in SOD and NO levels and decreased the release of MDA.

Conclusions: This gastroprotective effect of biochanin A could be attributed to the enhancement of cellular metabolic cycles perceived as an increase in the SOD, NO activity, and decrease in the level of MDA, and also decrease in level of Bax expression and increase the Hsp70 expression level.

Publication types

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

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Ethanol
  • Female
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / pathology*
  • Gastric Mucosa / physiopathology
  • Genistein / pharmacology
  • Genistein / therapeutic use*
  • HSP70 Heat-Shock Proteins / metabolism
  • Immunohistochemistry
  • Liver Function Tests
  • Malondialdehyde / metabolism
  • Nitric Oxide / metabolism
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Rats, Sprague-Dawley
  • Staining and Labeling
  • Stomach Ulcer / chemically induced*
  • Stomach Ulcer / drug therapy*
  • Stomach Ulcer / pathology
  • Stomach Ulcer / physiopathology
  • Superoxide Dismutase / metabolism
  • Toxicity Tests, Acute
  • bcl-2-Associated X Protein / metabolism

Substances

  • Antioxidants
  • HSP70 Heat-Shock Proteins
  • Protective Agents
  • bcl-2-Associated X Protein
  • Nitric Oxide
  • Ethanol
  • Malondialdehyde
  • Genistein
  • Superoxide Dismutase
  • biochanin A

Grants and funding

The authors would like to thank the University of Malaya for supporting this project PV069-2012A, and HIR-MOHE (F000009-21001) from the Ministry of Higher Education Malaysia. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.