Assessment of Gastroprotective Potential of Delonix regia (Boj Ex Hook) Raf against Ethanol and Cold Restrain Stress-Induced Ulcer in Rats
Purpose: To assess the gastroprotective potential of the stem bark ethanol extract of Delonix regia (EDR) on ethanol and cold restrain stress-induced ulcer in experimental rats. Methods: EDR (100, 200 and 400 mg/kg doses, orally) was evaluated on ethanol and cold restrain stress-induced ulcer in exp...
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Veröffentlicht in: | Tropical journal of pharmaceutical research 2015-07, Vol.14 (6), p.1063 |
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Sprache: | eng |
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Zusammenfassung: | Purpose: To assess the gastroprotective potential of the stem bark
ethanol extract of Delonix regia (EDR) on ethanol and cold restrain
stress-induced ulcer in experimental rats. Methods: EDR (100, 200 and
400 mg/kg doses, orally) was evaluated on ethanol and cold restrain
stress-induced ulcer in experimental rats. In ethanol induced ulcer
model, ulcer index, percent protection, reduced glutathione (GSH),
malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT),
myeloperoxidase (MPO), cytokines and nitric oxide (NO) levels in
stomach tissue were evaluated. In the cold restrain stress model, ulcer
index, percent protection, and GSH levels were evaluated.
2,2-Diphenyl-1-picryl hydrazyl (DPPH) radical scavenging assay of EDR
was also performed. Results: EDR caused a significant (p <
0.05-0.001) decreased ulcer index in ethanol (61.33-76.00%) and cold
restrain stress (47.34-84.28 %) models. The EDR caused a significant (p
< 0.05 - 0.001) increase in SOD (0.20 - 0.27 U/mg protein, CAT (200
-270 μmole H2O2/mg of protein/minute), GSH (1.63 - 1.17 μg/mg
protein) and reduction in nitric oxide (NO) level, pro-inflammatory
cytokine (TNF-αand IL-6) levels and inhibition in neutrophil
accumulation (p < 0.001) in ethanol-induced model. EDR exhibited
significant antioxidant activity with IC50 value of 45.23 ± 3.23
μg/ml. Conclusion: The results suggest that EDR has
gastroprotective effect in the two ulcer models and this may be due to
its antioxidant effect. |
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ISSN: | 1596-5996 1596-9827 |
DOI: | 10.4314/tjpr.v14i6.18 |