首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Comparative study of the cytotoxic effect of microcistin-LR and purified extracts from Microcystis aeruginosa on a kidney cell line
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Comparative study of the cytotoxic effect of microcistin-LR and purified extracts from Microcystis aeruginosa on a kidney cell line

机译:Microcistin-LR和铜绿微囊藻纯化提取物对肾细胞系的细胞毒性作用的比较研究

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摘要

Microcystin-LR (MCLR) is a potent hepatotoxin, but increasing evidences suggest that it might also induce kidney injury. The aim of this work was to evaluate the cytotoxicity of MCLR on a kidney cell line (Vero-E6). Cells were exposed for up to 72 h either to Microcystis aeruginosa extracts from both MCLR-producer and non-MCLR-producer isolates or to pure MCLR (1.5-200 mu M). The cytotoxic effects were evaluated by several cell viability assays (MTT, Neutral Red and LDH). Pure MCLR, the extract fromMCLR-producer and the mixture of the non-MCLR-producer with pure MCLR, induced cell viability decrease in a similar dose/time-dependent manner. Conversely, no effects were induced by the extract of non-MCLR-producer. These results suggest that the cytotoxic effects of M. aeruginosa extract were due to MCLR and excluded the eventual toxicity of other cyanobacteria bioactive compounds. The lowest cytotoxic MCLR concentration varied between 11 and 100 |iM depending on the employed cell viability assay andis within the range of MCLR dosage reported to affect other mammalian cell lines. The NR assay was the most sensitive to evaluate the MCLR-induced cytotoxicity. Our results suggest that Vero-E6 cell line may constitute a cell model to evaluate the nephrotoxicity of microcystins.
机译:微囊藻毒素-LR(MCLR)是有效的肝毒素,但越来越多的证据表明它也可能诱发肾脏损伤。这项工作的目的是评估MCLR对肾细胞系(Vero-E6)的细胞毒性。将细胞暴露于来自MCLR生产者和非MCLR生产者的铜绿微囊藻提取物或纯MCLR(1.5-200μM)暴露长达72小时。通过几种细胞活力测定(MTT,中性红和LDH)评估了细胞毒性作用。纯MCLR,MCLR生产者的提取物以及非MCLR生产者与纯MCLR的混合物,诱导的细胞活力以相似的剂量/时间依赖性方式降低。相反,非MCLR生产者的提取物未引起作用。这些结果表明铜绿假单胞菌提取物的细胞毒性作用归因于MCLR,但排除了其他蓝细菌生物活性化合物的最终毒性。最低的细胞毒性MCLR浓度在11至100μM之间变化,具体取决于所采用的细胞生存力测定,并且在报告影响其他哺乳动物细胞系的MCLR剂量范围内。 NR分析对评估MCLR诱导的细胞毒性最敏感。我们的结果表明,Vero-E6细胞系可能构成评估微囊藻毒素的肾毒性的细胞模型。

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