Subapriya R, Kumaraguruparan R, Abraham S K, Nagini S
Department of Biochemistry, Faculty of Science, Annamalai University, Annamalainagar-608 002, Tamil Nadu, India.
Drug Chem Toxicol. 2004 Feb;27(1):15-26. doi: 10.1081/dct-120027894.
We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduced glutathione (GSH), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) were used as intermediate biomarkers of chemoprotection. Animals were divided into four groups of five animals each. Animals in group 1 were given MNNG (40 mg/kg body weight) by intragastric intubation. Animals in group 2 received intragastric administration of ethanolic neem leaf extract at a concentration of 200 mg/kg body weight for 5 days followed by MNNG 1.5 h after the final feeding. Group 3 animals received ethanolic neem leaf extract alone for five days. Group 4 received the same volume of normal saline and served as control. The animals were sacrificed by cervical dislocation 27 h after the carcinogen exposure. In MNNG-treated mice, enhanced lipid peroxidation with compromised antioxidant defences in the stomach, liver and erythrocytes was accompanied by increase in bone marrow micronuclei. Pretreatment with ethanolic neem leaf extract significantly reduced MNNG-induced micronuclei and lipid peroxides and enhanced GSH-dependent antioxidant activities. The results of the present study demonstrate that ethanolic neem leaf extract exerts protective effects against MNNG-induced genotoxicity and oxidative stress by augmenting host antioxidant defence mechanisms.
我们评估了乙醇提取物预处理对N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的雄性瑞士白化小鼠遗传毒性和氧化应激的影响。微核(MN)频率、脂质过氧化物浓度以及抗氧化剂还原型谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽-S-转移酶(GST)的状态被用作化学保护的中间生物标志物。将动物分为四组,每组五只。第1组动物通过胃内插管给予MNNG(40mg/kg体重)。第2组动物以200mg/kg体重的浓度胃内给予乙醇提取物,持续5天,最后一次喂食后1.5小时给予MNNG。第3组动物单独接受乙醇提取物5天。第4组给予相同体积的生理盐水作为对照。致癌物暴露27小时后,通过颈椎脱臼处死动物。在MNNG处理的小鼠中,胃、肝脏和红细胞中脂质过氧化增强,抗氧化防御受损,同时骨髓微核增加。乙醇提取物预处理显著降低了MNNG诱导的微核和脂质过氧化物,并增强了GSH依赖性抗氧化活性。本研究结果表明,乙醇提取物通过增强宿主抗氧化防御机制,对MNNG诱导的遗传毒性和氧化应激发挥保护作用。