Farombi E O, Adepoju B F, Ola-Davies O E, Emerole G O
Drug Metabolism and Toxicology Unit, Department of Biochemistry, College of Medicine, University of Ibadan, Nigeria.
Eur J Cancer Prev. 2005 Jun;14(3):207-14. doi: 10.1097/00008469-200506000-00003.
The chemopreventive effects of kolaviron, a natural antioxidant bioflavonoid from the seeds of Garcinia kola, on aflatoxin B1 (AFB1)-induced genotoxicity and hepatic oxidative damage was investigated in rats. Kolaviron administered 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 (gamma-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 gamma-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.
研究了可乐维隆(一种从可乐果种子中提取的天然抗氧化生物类黄酮)对黄曲霉毒素B1(AFB1)诱导的大鼠遗传毒性和肝脏氧化损伤的化学预防作用。在AFB1(2mg/kg,单次腹腔注射)处理的前2周,每天口服一次剂量为200mg/kg的可乐维隆,然后在最后4周每天口服两次剂量为100mg/kg的可乐维隆,结果显示其使AFB1诱导的天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)和γ-谷氨酰转移酶(γ-GT)活性增加分别降低了62%、56%和72%。在AFB1处理的大鼠肝脏中观察到丙二醛(MDA)形成和脂质氢过氧化物(LHP)积累。可乐维隆显著降低了AFB1诱导的MDA和LHP形成。维生素C和E在降低AFB1引起的AST、ALT和γ-GT活性增加以及脂质过氧化方面具有保护作用(P<0.01)。单独给大鼠服用可乐维隆导致谷胱甘肽S-转移酶、尿苷葡糖醛酸基转移酶和NADH:醌氧化还原酶的活性分别显著升高2.45倍、1.62倍和1.38倍。此外,可乐维隆减弱了AFB1介导的这些酶活性的降低(P<0.01)。单独用可乐维隆、维生素C和E预处理大鼠,通过微核多染红细胞(MNPCEs)形成评估未显示出遗传毒性(P>0.05)。在AFB1(1mg/kg)给药前30分钟和给药后30分钟腹腔注射可乐维隆(500mg/kg)共同处理大鼠,72小时后抑制了AFB1诱导的MNPCEs(P<0.001)。虽然维生素C有效降低了AFB1诱导的MNPCEs形成,但维生素E未引发任何抗遗传毒性反应。这些结果表明可乐维隆是对抗AFB1诱导的遗传毒性和肝脏氧化应激的有效化学预防剂。因此,可乐维隆可能有资格在食品受黄曲霉毒素污染的流行地区进行临床试验,以对抗黄曲霉毒素中毒的威胁。