首页> 外文期刊>Acta Poloniae Pharmaceutica: Durg Research >Anti-clastogenic activity of Azadirachta indica against benzo(a)pyrene in murine forestomach tumorigenesis bioassay.
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Anti-clastogenic activity of Azadirachta indica against benzo(a)pyrene in murine forestomach tumorigenesis bioassay.

机译:在鼠前胃癌成瘤生物测定中,印za印对苯并(a)py的抗破灭活性。

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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.
机译:摘要:本研究在鼠前胃癌发生生物测定方案中评估了印za(A。indica)对苯并(a)py [B(a)P]的抗破灭作用。将雌性Balb / c小鼠分为四组(n = 8)。来自B(a)P和B(a)P +印度。组的每只小鼠均接受40 mg / kg b剂量的B(a)P胃内滴注。 w。从实验的第3周到第6周结束,每周两次加入0.2 mL橄榄油。对照组和印度A组的小鼠接受与B(a)P和B(a)P + A d组相同的时间表的0.2 mL橄榄油。 A. indica和B(a)P + A. indica组的小鼠接受100 mg / kg b的口服剂量。 w。在整个实验过程中的隔几天,将A树叶片水提取物(AAILE)提取。最后一次B(a)P滴注后两周,处死小鼠并处理脾脏进行微核(MN)测定,同时分析肝组织的脂质过氧化(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滴注的小鼠脾细胞中MN形成的发生率增加。在肝组织中,滴注B(a)P后氧化应激的程度增加,这可以从仅接受B(a)P滴注的小鼠中升高的LPO水平伴随着抗氧化防御酶活性的降低而得到证明。有趣的是,与仅接受B(a)P的小鼠相比,印度。虫的治疗显着逆转了在接受AAILE和B(a)P的小鼠中观察到的这些作用。此外,仅在接受AAILE的小鼠中,观察到增强的抗氧化剂防御能力,LPO水平以及MN发病率略有降低。本研究的观察结果表明,印度A草通过调节氧化应激和抗氧化防御作用而对B(a)P发挥抗生胶作用。

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