Gangar Subhash Chander, Sandhir Rajat, Koul Ashwani
Department of Biophysics, Basic Medical Sciences Block, Panjab University, Chandigarh, 160014, India.
Acta Pol Pharm. 2010 Jul-Aug;67(4):381-90.
Abstract: Present study evaluated the anti-clastogenic efficacy of Azadirchta indica (A. indica) against benzo(a)pyrene [B(a)P] in murine forestomach tumorigenesis bioassay protocol. Female Balb/c mice were divided into four groups (n = 8). Each mouse from B(a)P and B(a)P + A. indica groups received intragastric instillations of B(a)P at a dose of 40 mg/kg b. w. in 0.2 mL olive oil twice a week, starting from 3rd week to the end of 6th week of the experiment. Mice of control and A. indica groups received 0.2 mL olive oil in the same schedule as for B(a)P and B(a)P + A indica groups. Mice of A. indica and B(a)P + A. indica groups received oral doses of 100 mg/kg b. w. aqueous A. indica leaf extract (AAILE) on alternate days throughout the experiment. Two weeks after the last B(a)P instillation, mice were sacrificed and spleens were processed for micronucleus (MN) assay, while liver tissues were analyzed for lipid peroxidation (LPO), as well as antioxidant defense enzymes, namely: catalase, superoxide dismutase (SOD), glutathione reductase (GR) and glutathione peroxidase (GPx). The incidence of MN formation increased in spleen cells of mice that received only B(a)P instillations. In hepatic tissues, the extent of oxidative stress increased upon B(a)P instillations as was evidenced from enhanced LPO levels with concomitant decrease in antioxidant defense enzyme activities in mice that received only B(a)P instillations. Interestingly, A. indica treatment significantly reversed these effects as observed in mice receiving AAILE along with B(a)P when compared to only B(a)P receiving mice. Moreover, in only AAILE receiving mice, enhanced antioxidant defense with slightly decreased levels of LPO as well as MN incidences were observed. Observations of the present study suggest that A. indica exert anticlastogenic effects against B(a)P by modulating oxidative stress and antioxidant defense.
本研究在小鼠前胃肿瘤发生生物测定方案中评估了印度楝(Azadirchta indica,A. indica)对苯并(a)芘[B(a)P]的抗致断裂作用。将雌性Balb/c小鼠分为四组(n = 8)。从实验第3周开始至第6周结束,B(a)P组和B(a)P + A. indica组的每只小鼠每周两次经胃内灌胃给予剂量为40 mg/kg体重的B(a)P,溶于0.2 mL橄榄油中。对照组和A. indica组的小鼠按与B(a)P组和B(a)P + A. indica组相同的时间表给予0.2 mL橄榄油。A. indica组和B(a)P + A. indica组的小鼠在整个实验期间每隔一天经口给予剂量为100 mg/kg体重的印度楝叶水提取物(AAILE)。在最后一次灌胃B(a)P两周后,处死小鼠并取脾脏进行微核(MN)测定,同时分析肝脏组织的脂质过氧化(LPO)以及抗氧化防御酶,即过氧化氢酶、超氧化物歧化酶(SOD)、谷胱甘肽还原酶(GR)和谷胱甘肽过氧化物酶(GPx)。仅接受B(a)P灌胃的小鼠脾脏细胞中微核形成的发生率增加。在肝脏组织中,仅接受B(a)P灌胃的小鼠中,B(a)P灌胃后氧化应激程度增加,这从LPO水平升高以及抗氧化防御酶活性同时降低得到证明。有趣的是,与仅接受B(a)P的小鼠相比,在接受AAILE和B(a)P的小鼠中观察到,印度楝处理显著逆转了这些效应。此外,在仅接受AAILE的小鼠中,观察到抗氧化防御增强,LPO水平略有降低以及微核发生率降低。本研究的观察结果表明,印度楝通过调节氧化应激和抗氧化防御对B(a)P发挥抗致断裂作用。