...
首页> 外文期刊>Journal of international management >Dose- and Time-dependent Effects of Permethrin on HepG2 Cells: Cell Survival, Lipid Peroxidation and Antioxidant Defence System
【24h】

Dose- and Time-dependent Effects of Permethrin on HepG2 Cells: Cell Survival, Lipid Peroxidation and Antioxidant Defence System

机译:PEPRENRIN对HEPG2细胞的剂量和时间依赖性作用:细胞存活,脂质过氧化和抗氧化防御系统

获取原文
获取原文并翻译 | 示例

摘要

There is very limited knowledge about in vitro hepatotoxicity of permethrin concerning dose and duration even though humans and nontargeted beings are exposed. In this study, three different doses of permethrin (1 mu M, 10 mu M, 100 mu M) were administered in three different time periods (24, 48, 72 h) and cell viability (WST-1 and Trypan blue test), lipid peroxidation (high performance lipid chromatography), and antioxidant (SOD-1, SOD-2 and GPx-1) gene expression levels (real time PCR) were evaluated. The LC50 dose of permethrin was calculated as 1111 mu M. Significant decrease in cell viability was detected in every time period except at the lowest dose (P<0.05). Each permethrin dose caused a significant increase (P<0.01) in superoxide dismutase-1 levels (except 1 tiM at 48 h). The 10 mu M and 100 mu NI groups' superoxide dismutase-2 levels were higher than the controls at each exposure level though the 1 mu M group was significantly lower at 24 and 48 h and higher at 72 h. Interestingly, a non-uniform statistically significant difference for glutathione peroxidase-1 was seen in each exposure duration and doses either as up- or down regulation (P<0.01). Generally, malondialdehyde concentrations were significantly increased (P<0.01), although at each dose in 72 h a significant decrease in malonaldehyde levels was seen (P<0.01). Our results may help in understanding the molecular aspects of high dose permethrin hepatotoxicity. More comprehensive research is required to evaluate long term low dose exposure.
机译:对于莫西蛋白的体外肝毒性有关剂量和持续时间的高度知识,即使人类和不确定的生物暴露。在该研究中,在三种不同的时间段(24,48,72h)和细胞活力(WST-1和Trypan Blue Test)中施用三种不同剂量的滤液(1μm,10μm,100μm),评价脂质过氧化(高性能脂质色谱)和抗氧化剂(SOD-1,SOD-2和GPX-1)基因表达水平(实时PCR)。渗透素的LC50剂量计算为1111μm。除了最低剂量之外,在每次段中检测到细胞活力的显着降低(P <0.05)。每种渗透素剂量在超氧化物歧化酶-1水平中引起显着增加(P <0.01)(在48小时内除外。 10μm和100μln的超氧化物歧化酶-2水平高于每种曝光水平的对照,尽管在24和48小时的情况下显着降低,72小时较高。有趣的是,在每个曝光持续时间内观察到谷胱甘肽过氧化物酶-1的非均匀统计学显着差异,并剂量为上下调节(P <0.01)。通常,丙二醛浓度明显增加(P <0.01),尽管在72小时内每剂量进行显着降低,但是(P <0.01)。我们的结果可能有助于了解高剂量氯菊酯肝毒性的分子方面。需要更全面的研究来评估长期低剂量暴露。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号