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DC Field | Value | Language |
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dc.contributor.author | Farombi, E. O. | - |
dc.contributor.author | Adepoju, B. F. | - |
dc.contributor.author | Ola-Davies, O. E. | - |
dc.contributor.author | Emerole, G. O. | - |
dc.date.accessioned | 2021-06-02T14:32:38Z | - |
dc.date.available | 2021-06-02T14:32:38Z | - |
dc.date.issued | 2005 | - |
dc.identifier.issn | 0959-8278 | - |
dc.identifier.other | ui_art_farombi_chemoprevention_2005 | - |
dc.identifier.other | European Journal of Cancer prevention 14, pp. 207-214 | - |
dc.identifier.uri | http://ir.library.ui.edu.ng/handle/123456789/5375 | - |
dc.description.abstract | The chemopreventive effects of kolaviron, a natural antioxidant biflavonoid from the seeds of Garcinia kola, on aflatoxin B1 (AFB1)-induced genotoxicity and hepatic oxidative damage was investigated in rats. Kolavironmadministered orally at a dose of 200 mg/kg once a day for the first 2 weeks and then 100 mg/kg twice a day for the last 4 weeks of AFB1 (2 mg/kg, single dose, intraperitoneal) treatment reduced the AFB1-increased activities of aspartate amino transferase (AST), alanine amino transferase (ALT) and gamma glutamyltransferase (c-GT) by 62%, 56% and 72% respectively. Malondialdehyde (MDA) formation and lipid hydroperoxide (LHP) accumulation were observed in the livers of AFB1-treated rats. Kolaviron significantly reduced the AFB1-induced MDA and LHP formation. Vitamins C and E were protective in reducing the increase in the activities of AST, ALT and c-GT as well as lipid peroxidation caused by AFB1 (P < 0.01). Administration of rats with kolaviron alone resulted in significant elevation in the activities of glutathione S-transferase, uridyl glucuronosyl transferase and NADH:quinone oxidoreductase by 2.45-, 1.62- and 1.38-folds respectively. In addition, kolaviron attenuated the AFB1-mediated decrease in the activities of these enzymes (P < 0.01). Pretreatment of rats with kolaviron, vitamins C and E alone did not exert genotoxicity assessed by the formation of micronucleated polychromatic erythrocytes (MNPCEs) (P> 0.05). Co-treatment of rats intraperitoneally with kolaviron (500 mg/kg) 30 min before and 30 min after AFB1 (1 mg/kg) administration inhibited the induction of MNPCEs by AFB1 (P < 0.001) after 72 h. While vitamin C was effective in reducing AFB1- induced MNPCEs formation, vitamin E did not elicit any antigenotoxic response. These results indicate kolaviron as effective chemopreventive agent against AFB1-induced genotoxicity and hepatic oxidative stress. Thus kolaviron may qualify for clinical trial in combating the menace of aflatoxicosis in endemic areas of aflatoxin contamination of foods. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.subject | Aflatoxin B1 | en_US |
dc.subject | Antioxidants | en_US |
dc.subject | Chemoprevention | en_US |
dc.subject | Garcinia kola | en_US |
dc.subject | Genotoxicity | en_US |
dc.subject | Hepatotoxicity | en_US |
dc.subject | Kolaviron | en_US |
dc.subject | Micronuclei | en_US |
dc.title | Chemoprevention of aflatoxin B1-induced genotoxicity and hepatic oxidative damage in rats by kolaviron, a natural biflavonoid of garcinia kola seeds | en_US |
dc.type | Article | en_US |
Appears in Collections: | scholarly works |
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