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首页> 外文期刊>Cytotechnology >Eicosapentaenoic acid protects against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced hepatic toxicity in cultured rat hepatocytes
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Eicosapentaenoic acid protects against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced hepatic toxicity in cultured rat hepatocytes

机译:二十碳五烯酸可保护2,3,7,8-四氯二苯并-p-二恶英诱导的大鼠肝细胞肝毒性

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摘要

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a persistent and ubiquitous environmental contaminant. The health impact of TCDD exposure is of great concern to the general public. Recent reports have implied that eicosapentaenoic acid (EPA) might be a potential chemopreventive agent and influence hepatotoxicity. The aim of the current study was to explore the effectiveness of EPA in alleviating the toxicity of TCDD on primary cultured rat hepatocytes. EPA (5, 10 and 20 μM) was added to cultures alone or simultaneously with TCDD (5 and 10 μM). Rat hepatocytes were treated with TCDD and EPA for 48 h, and then cytotoxicity was detected by [3-(4,5-dimethyl-thiazol-2-yl) 2,5-diphenyltetrazolium bromide] (MTT) assay and lactate dehydrogenase (LDH) release, while total antioxidant capacity (TAC) and total oxidative stress (TOS) levels were determined to evaluate the oxidative injury. The DNA damage was also analyzed by liver micronucleus assay (LMN) and 8-oxo-2-deoxyguanosine (8-OH-dG). The results of MTT and LDH assays showed that TCDD but not EPA decreased cell viability. TCDD also increased TOS level and significantly decreased TAC level in rat hepatocytes in a clear dose dependent manner. On the basis of increasing doses, the dioxin caused significant increases of micronucleated hepatocytes (MNHEPs) and 8-OH-dG as compared to control culture. Whereas, in cultures treated with EPA alone, TOS level did not change and the level of TAC significantly increased. The presence of EPA with TCDD minimized the toxic effects of the dioxin on primary hepatocytes cultures. Noteworthy, EPA has a protective effect against TCDD-mediated DNA damages.
机译:2,3,7,8-四氯二苯并-对-二恶英(TCDD)是一种持久存在且普遍存在的环境污染物。 TCDD暴露对健康的影响引起了公众的极大关注。最近的报道暗示二十碳五烯酸(EPA)可能是一种潜在的化学预防剂并影响肝毒性。本研究的目的是探索EPA在减轻TCDD对原代培养的大鼠肝细胞毒性方面的有效性。将EPA(5、10和20μM)单独或与TCDD(5和10μM)同时添加到培养物中。用TCDD和EPA处理大鼠肝细胞48小时,然后通过[3-(4,5-二甲基噻唑-2-基)2,5-二苯基四唑溴化](MTT)测定法和乳酸脱氢酶(LDH)检测细胞毒性释放),同时确定总抗氧化能力(TAC)和总氧化应激(TOS)水平以评估氧化损伤。还通过肝微核试验(LMN)和8-氧-2-脱氧鸟苷(8-OH-dG)分析了DNA损伤。 MTT和LDH分析的结果表明TCDD降低了细胞活力,但EPA却没有。 TCDD还以明显的剂量依赖性方式增加了大鼠肝细胞的TOS水平并显着降低了TAC水平。在增加剂量的基础上,与对照培养相比,二恶英导致微核肝细胞(MNHEPs)和8-OH-dG显着增加。而在单独用EPA处理的培养物中,TOS水平没有变化,TAC的水平也显着增加。带有TCDD的EPA的存在将二恶英对原代肝细胞培养的毒性作用降至最低。值得注意的是,EPA对TCDD介导的DNA损伤具有保护作用。

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