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首页> 外文期刊>European journal of cancer prevention: The official journal of the European Cancer Prevention Organisation (ECP) >Chemoprevention of aflatoxin B1-induced genotoxicity and hepatic oxidative damage in rats by kolaviron, a natural bioflavonoid of Garcinia kola seeds.
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Chemoprevention of aflatoxin B1-induced genotoxicity and hepatic oxidative damage in rats by kolaviron, a natural bioflavonoid of Garcinia kola seeds.

机译:黄藻毒素(一种藤黄可乐种子的天然生物类黄酮)化学预防黄曲霉毒素B1诱导的大鼠遗传毒性和肝氧化损伤。

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摘要

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.
机译:研究了鼠李子(一种来自藤黄种子的天然抗氧化剂生物类黄酮)对黄曲霉毒素B1(AFB1)诱导的遗传毒性和肝氧化损伤的化学预防作用。在头2周内每天一次以200 mg / kg的剂量口服Kolaviron,然后在后4周内每天两次以100 mg / kg的剂量对AFB1(2 mg / kg,单剂量,腹膜内)治疗降低AFB1谷草转氨酶(AST),丙氨酸转氨酶(ALT)和γ-谷氨酰转移酶(γ-GT)的活性分别增加了62%,56%和72%。在AFB1处理的大鼠肝脏中观察到丙二醛(MDA)的形成和脂质过氧化氢(LHP)的积累。 Kolaviron大大减少了AFB1诱导的MDA和LHP的形成。维生素C和E对减少AFB1引起的AST,ALT和γ-GT活性增加以及脂质过氧化具有保护作用(P <0.01)。单独施用科拉沃龙的大鼠可导致谷胱甘肽S-转移酶,尿苷葡萄糖醛糖苷基转移酶和NADH:醌氧化还原酶的活性分别显着升高2.45倍,1.62倍和1.38倍。此外,科拉弗龙减弱了AFB1介导的这些酶活性的降低(P <0.01)。单独用维生素K和维生素E预处理的大鼠未产生通过形成微核多色红细胞(MNPCE)评估的遗传毒性(P> 0.05)。在AFB1(1 mg / kg)给药前30分钟和后30分钟,腹腔内用克拉维铁(500 mg / kg)共同治疗大鼠,72 h后AFB1诱导MNPCEs抑制(P <0.001)。尽管维生素C可有效减少AFB1诱导的MNPCE的形成,但维生素E不会引起任何抗原毒性反应。这些结果表明,钴铁蛋白是对抗AFB1诱导的遗传毒性和肝氧化应激的有效化学预防剂。因此,在食品中黄曲霉毒素污染的流行地区,克拉维龙可能有资格对抗黄曲霉病的威胁进行临床试验。

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