首页> 外文期刊>Journal of environmental pathology, toxicology and oncology: official organ of the International Society for Environmental Toxicology and Cancer >Aqueous Extract of Smokeless Tobacco (gutkha) Deregulates Tumor Suppressor and DNA Repair Response in a Murine Model of Smokeless Tobacco Use
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Aqueous Extract of Smokeless Tobacco (gutkha) Deregulates Tumor Suppressor and DNA Repair Response in a Murine Model of Smokeless Tobacco Use

机译:无烟烟草(Gutkha)的水质提取物放松无烟烟草使用的小鼠模型中的肿瘤抑制器和DNA修复反应

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The effect of smokeless tobacco (gutkha) was investigated by treating male and female Swiss Albino mice with an aqueous extract of smokeless tobacco (AEST). AEST was administered at a dose of 25 mg kg(-1) body weight per day for different time periods (6, 12, 16, and 24 weeks), and control animals were provided only drinking water without AEST for the same period. Control and AEST-treated mice were observed for different oxidative stress parameters, nitric oxide (NO) release, and myeloperoxidase (MPO) release, and they were evaluated for alterations in tumor suppressor and DNA repair responses in the liver and spleen. Both male and female mice treated with AEST showed significant increase in lipid peroxidation, protein carbonylation, and NO and MPO release in the liver and spleen compared to age-and gender-matched controls. The significant decline in tumor suppressor p53 protein levels, likely mediated by concomitantly upregulated levels of Mdm2, was observed. We also observed a significant decline in the levels of DNA repair proteins Brca2 and Ape-1 compared to the respective controls. Thus, AEST induces oxidative stress, inflammation, and significantly lowers tumor suppressor and DNA repair responses. These factors may work in conjunction to increase the risk for certain diseases, including cancer.
机译:通过用无烟烟草(最可爱)的含水提取物来调查无烟烟草(Gutkha)的效果。在不同时间段(6,12,16和24周)每天以25mg kg(-1)体重(6,12,16和24周)给药,并且对照动物仅在同一时期的情况下仅提供饮用水。观察到不同氧化应激参数,一氧化氮(NO)释放和髓过氧化物酶(MPO)释放的对照和最美处理的小鼠,并评估肝脏和脾脏中肿瘤抑制剂和DNA修复反应的改变。与年龄和性别匹配的对照相比,用最含量处理的血液过氧化,蛋白质羰基化和NO和MPO释放的血液过氧化,蛋白质羰基化和NO和MPO释放的两种雄性和雌性小鼠均显示出肝脏和脾脏。观察到肿瘤抑制器P53蛋白水平的显着下降,可能通过伴随的MDM2伴随的MDM2水平介导。与相应的对照相比,我们还观察到DNA修复蛋白BRCA2和APE-1的水平显着下降。因此,最目的因诱导氧化应激,炎症,并且显着降低肿瘤抑制和DNA修复反应。这些因素可以结合使用患有癌症的某些疾病的风险。

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