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首页> 外文期刊>In vivo. >Chemopreventive Action by Ethanol-extracted Brazilian Green Propolis on Post-initiation Phase of Inflammation-associated Rat Colon Tumorigenesis
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Chemopreventive Action by Ethanol-extracted Brazilian Green Propolis on Post-initiation Phase of Inflammation-associated Rat Colon Tumorigenesis

机译:乙醇提取的巴西绿蜂胶对炎症相关大鼠结肠肿瘤发生后启动阶段的化学预防作用。

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Background/Aim: Propolis has since long been utilized in numerous folk medicines with a variety of medicinal properties. In this study, the effects of ethanol-extracted (EEP) and water-extracted (WEP) Brazilian green propolis on the post-initiation phase of inflammation-associated rat colon tumorigenesis were directly compared. Materials and Methods: Male F344 rats at 6 weeks of age were subcutaneously injected with 1,2-dimethylhydrazine (DMH) at 40 mg/kg body weight twice during the first week, followed by 1% dextran sodium sulfate (DSS) in drinking water for one week. After a 1-week no-treatment period, animals were administered either basal Oriental MF powdered diet, or 1% EEP or 1% WEP in the basal diet until week 32. Results: Post-initiation treatment with EEP significantly reduced the multiplicity of colorectal carcinomas compared to the control (0.40{+/-}0.13/rat vs. 2.29{+/-}0.84/rat, respectively, p<0.05), and EEP also reduced the tumor volume. Immunohistochemically, expression of inflammation-associated proteins inducible nitric oxide synthase, tumor necrotic factor alpha, nuclear factor kappa B and glutathione peroxidase-2 were significantly diminished in colorectal tumors from EEP-treated rats. Conclusion: Suppression of inflammation and oxidative stress, which had been triggered by DMH and promoted by DSS, was a primary mechanism by which EEP suppressed carcinogenesis.
机译:背景/目的:蜂胶长期以来被广泛用于多种具有多种医学特性的民间药物中。在这项研究中,直接比较了乙醇提取(EEP)和水提取(WEP)巴西绿色蜂胶对炎症相关大鼠结肠肿瘤发生的初始阶段的影响。材料和方法:在6周龄的雄性F344大鼠中,在第一周两次皮下注射40 mg / kg体重的1,2-二甲基肼(DMH),然后在饮用水中注射1%的葡聚糖硫酸钠(DSS)一周。经过1周的无治疗期后,动物接受了基础东方MF粉饮食或基础饮食中1%EEP或1%WEP的饮食,直到第32周为止。结果:EEP的初始治疗显着降低了结直肠的多样性与对照组相比(0.40 {+/-} 0.13 / rat vs. 2.29 {+/-} 0.84 / rat,分别为p <0.05),并且EEP也减少了肿瘤体积。免疫组化显示,在EEP处理的大鼠的大肠肿瘤中,炎症相关蛋白可诱导的一氧化氮合酶,肿瘤坏死因子α,核因子κB和谷胱甘肽过氧化物酶2的表达显着降低。结论:由DMH引发并由DSS促进的炎症和氧化应激的抑制是EEP抑制癌变的主要机制。

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