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Protective effects of garlic oil on hepatocarcinoma induced by N-nitrosodiethylamine in rats

机译:大蒜油对N-亚硝基二乙胺诱导的大鼠肝癌的保护作用

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摘要

To investigate the protective effects and the possible mechanisms of garlic oil (GO) against N-nitrosodiethylamine (NDEA)-induced hepatocarcinoma in rats Wistar rats were gavaged with GO (20 or 40 mg/kg) for 1 week and then were gavaged with GO and NDEA (10 mg/kg) for the next 20 weeks. The changes of morphology histology the biochemical indices of serum and DNA oxidative damage of liver were examined to assess the protective effects. Lipid peroxidation (LPO) antioxidant defense system and apoptosis-related proteins were measured to investigate potential mechanisms. At the end of the study (21 weeks) GO administration significantly inhibited the increase of the nodule incidence and average nodule number per nodule-bearing liver induced by NDEA improved hepatocellular architecture and dramatically inhibited NDEA-induced elevation of serum biochemical indices (alanine aminotransferase aspartate aminotransferase alkaline phosphatase and gamma-glutamyl transpeptidase) and hepatic 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels in a dose-dependent manner. The mechanistic studies demonstrated that GO counteracted NDEA-induced oxidative stress in rats illustrated by the restoration of glutathione (GSH) superoxide dismutase (SOD) catalase (CAT) glutathione reductase (GR) glutathione peroxidase (GPx) glutathione-S-transferase (GST) levels and the reduction of the malondialdehyde (MDA) levels in liver. Furthermore the mRNA and protein levels of Bcl-2 Bcl-xl andβ -arrestin-2 were significantly decreased whereas those of Bax and caspase-3 were significantly increased. These data suggest that GO exhibited significant protection against NDEA-induced hepatocarcinogenesis which might be related with the enhancement of the antioxidant activity and the induction of apoptosis.
机译:为了研究大蒜油(GO)对N-亚硝基二乙胺(NDEA)诱导的大鼠肝癌的保护作用及其可能的机制,将Wistar大鼠用GO(20或40 mg / kg)灌胃1周,然后用GO灌胃并在接下来的20周内使用NDEA(10 mg / kg)。观察组织形态学变化,血清生化指标和肝脏DNA氧化损伤,以评价其保护作用。测量脂质过氧化(LPO)抗氧化防御系统和凋亡相关蛋白,以研究潜在的机制。在研究结束(21周)时,GO给药显着抑制了由NDEA引起的结节率的增加,每个结节性肝的平均结节数均​​改善了肝细胞结构,并显着抑制了NDEA引起的血清生化指标(丙氨酸氨基转移酶天冬氨酸)的升高氨基转移酶碱性磷酸酶和γ-谷氨酰转肽酶)和肝脏8-羟基-2'-脱氧鸟苷(8-OHdG)水平呈剂量依赖性。机理研究表明,GO可抵消大鼠NDEA诱导的氧化应激,这可以通过恢复谷胱甘肽(GSH)超氧化物歧化酶(SOD)过氧化氢酶(CAT)谷胱甘肽还原酶(GR)谷胱甘肽过氧化物酶(GPx)谷胱甘肽S-转移酶(GST)来说明肝脏中丙二醛(MDA)的水平降低。此外,Bcl-2,Bcl-xl和β-arrestin-2的mRNA和蛋白水平显着降低,而Bax和caspase-3的mRNA和蛋白水平显着升高。这些数据表明GO显示出对NDEA诱导的肝癌发生的显着保护,这可能与抗氧化剂活性的增强和细胞凋亡的诱导有关。

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