Subapriya R, Nagini S
Asian Pac J Cancer Prev. 2003 Jul-Sep;4(3):215-23.
We evaluated the effects of ethanolic neem leaf extract on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced gastric carcinogenesis in Wistar rats. The extent of lipid peroxidation and the status of the antioxidants superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH), glutathione peroxidase (GPx), and glutathione-S-transferase (GST) in the stomach, liver and erythrocytes were used as biomarkers of chemoprevention. Animals were divided into four groups of six animals each. Rats in group 1 were given MNNG (150 mg/kg bw) by intragastric intubation three times with a gap of 2 weeks in between the treatments. Rats in group 2 administered MNNG as in group 1, in addition received intragastric intubation of ethanolic neem leaf extract (200 mg/kg bw) three times per week starting on the day following the first exposure to MNNG and continued until the end of the experimental period. Group 3 animals were given ethanolic neem leaf extract alone, while group 4 served as controls. All the animals were killed after an experimental period of 26 weeks. Diminished lipid peroxidation in the stomach tumour tissue was associated with enhanced antioxidant levels. In contrast to tumour tissue, enhanced lipid peroxidation with compromised antioxidant defences was found in the liver and erythrocytes of tumour bearing animals. Administration of ethanolic neem leaf extract significantly reduced the incidence of stomach tumours, modulated lipid peroxidation and enhanced antioxidant status in the stomach, liver and blood. From the results of our study, we suggest that ethanolic neem leaf extract may exert its chemopreventive effects by modulating lipid peroxidation and enhancing the antioxidant status in the stomach, liver and erythrocytes.
我们评估了乙醇提取的印楝叶提取物对N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的Wistar大鼠胃癌发生的影响。胃、肝脏和红细胞中脂质过氧化程度以及抗氧化剂超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、还原型谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽-S-转移酶(GST)的状态被用作化学预防的生物标志物。将动物分为四组,每组六只。第1组大鼠通过胃内插管给予MNNG(150 mg/kg体重),共三次,每次给药间隔2周。第2组大鼠按第1组方式给予MNNG,此外,从首次接触MNNG后的第二天开始,每周三次通过胃内插管给予乙醇提取的印楝叶提取物(200 mg/kg体重),持续至实验期结束。第3组动物仅给予乙醇提取的印楝叶提取物,第4组作为对照。在26周的实验期后处死所有动物。胃肿瘤组织中脂质过氧化的减少与抗氧化剂水平的提高有关。与肿瘤组织相反,在荷瘤动物的肝脏和红细胞中发现脂质过氧化增强且抗氧化防御受损。给予乙醇提取的印楝叶提取物可显著降低胃肿瘤的发生率,调节脂质过氧化,并提高胃、肝脏和血液中的抗氧化状态。根据我们的研究结果,我们认为乙醇提取的印楝叶提取物可能通过调节脂质过氧化和提高胃、肝脏和红细胞中的抗氧化状态发挥其化学预防作用。