Premium
Attenuation of indomethacin‐ and HCl/ethanol‐induced oxidative gastric mucosa damage in rats by kolaviron, a natural biflavonoid of Garcinia kola seed
Author(s) -
Olaleye S. B.,
Farombi E. O.
Publication year - 2006
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.1793
Subject(s) - ranitidine , pharmacology , superoxide dismutase , glutathione , antioxidant , gastric mucosa , catalase , chemistry , ethanol , garcinia kola , lansoprazole , ulcer index , medicine , stomach , omeprazole , biochemistry , traditional medicine , enzyme
Reactive oxygen species (ROS) have been implicated in the aetiology of HCl/ethanol‐ and indomethacin gastric mucosal damage. This study investigated the protective effects of kolaviron, a natural antioxidant from the seed of Garcinia kola , on oxidative gastric mucosal damage induced by HCl/ethanol, and indomethacin. A HCl/ethanol mixture (1.5 mL of 0.15 n HCl in 70% ethanol) and indomethacin (IND) caused severe gastric damage with an ulcer index of 2.90 ± 0.8 and 2.5 ± 0.4, respectively, and significant reductions in the gastric mucosal content of catalase (CAT), superoxide dismutase (SOD) and glutathione (GSH) ( p < 0.001). Pre‐treatment of animals with kolaviron (100 mg/kg) orally 1 h and once daily for 3 days prior to ulcer induction significantly reduced the formation of ulcers induced by HCl/ethanol with preventive ratios of 65 and 72, respectively, while rats treated with kolaviron 1 day and for 7 days prior to IND treatment attenuated ulcer formation by 59% and 77%. Pre‐treatment with ranitidine 1 h prior to ulcer induction (50 mg/kg) elicited preventive ulcer ratio of 55. Kolaviron pre‐treatment 1 h before ulcer induction attenuated the HCl/ethanol reduction in CAT, SOD and GSH by 43%, 42% and 30%, respectively, and 67%, 68% and 64% following 72 h treatment with kolaviron. Ranitidine elicited 24%, 41% and 29% protective effects, respectively. Similarly, kolaviron administered to rats 1 day and for 7 days before IND treatment attenuated the drug‐induced inhibition of CAT by 44% and 70%; SOD by 23% and 43% and GSH by 32% and 55%, respectively. In a 1 h and 3‐day treatment with kolaviron before HCl/ethanol administration, MDA was reduced by 35% and 55%, respectively, while kolaviron administration 1 day and for 7 days before IND elicited a 39% and 58% reduction in MDA. Ranitidine elicited 39% and 50% reduction in MDA following HCl/ethanol and IND treatment. The results indicate the gastroprotective activity of kolaviron, which may be linked to its intrinsic antioxidant properties. Copyright © 2006 John Wiley & Sons, Ltd.