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An in vitro analysis of the rat C6 glioma cells to elucidate the linear alkylbenzene sulfonate induced oxidative stress and consequent G2/M phase cell cycle arrest and cellular apoptosis

机译:对大鼠C6胶质瘤细胞进行体外分析,以阐明直链烷基苯磺酸盐诱导的氧化应激以及随后的G2 / M期细胞周期阻滞和细胞凋亡

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摘要

Linear alkylbenzene Sulphonate (LAS) is the anionic surfactant component of globally consumed detergents. Exposure of sub-inhibitory fractions viz., 1/10th (T1), 1/5th (T2), and 1/2.5th (T3) of IC50 for 48 h, of LAS (5 mu M, 10 mu M, and 20 mu M, respectively) to viable C6 glioma cells of rat, besides imparting morphological alterations leads to gross cytotoxicity. Expression of the damaged DNA coupled with cleaved PARP (p 0.05; p 0.01 and p 0.001) were recorded for T1, T2 and T3, respectively. Subsequently, the cell cycle at G2/M check point was significantly arrested (p 0.05 for T1 and T2; p 0.01 for T3). The flow cytometric analysis reveals the initiation of apoptosis in C6 cells as is evident by a significant increase (p 0.01 for T1, p 0.001 for T2, and T3) in the intake of annexin-V, the calcium dependent apoptotic phospholipid binding protein. Moreover, significantly increased reactive oxygen species (ROS) (p 0.05; p 0.01 and p 0.001) after 6 h of exposure for all the three sets, registered a declining trend (P 0.001) when T3 cells were co-treated with N-acetyl cysteine (NAC). Furthermore, the significant attenuation (p 0.01) of expression of the cleaved PARP and a consequent decrease (p 0.05) in the cell cycle arrest at G2/M phase after scavenging ROS induced oxidative stress by treating C6 cells with NAC clearly evinces that LAS induced apoptosis is mediated by intracellular ROS. Thus, these findings provide a tangible basis for further investigations including in vivo studies, to unravel the molecular mechanism involved in ROS mediated and LAS induced cytotoxic manifestations. (C) 2018 Elsevier Ltd. All rights reserved.
机译:直链烷基苯磺酸盐(LAS)是全球消费的洗涤剂中的阴离子表面活性剂组分。 LAS(5μM,10μM和20)的IC50的亚抑制级分分别暴露于IC50的1/10(T1),1/5(T2)和1 / 2.5(T3)分别对每只鼠的C6胶质瘤细胞而言,除了赋予形态学改变外,还会导致总的细胞毒性。分别记录了T1,T2和T3受损DNA与裂解PARP的表达(p <0.05; p <0.01和p <0.001)。随后,在G2 / M检查点的细胞周期被显着停止(对于T1和T2,p <0.05;对于T3,p <0.01)。流式细胞仪分析显示,钙依赖性凋亡磷脂结合蛋白Annexin-V的摄入量显着增加(对于T1,p <0.01,对于T2和T3,p <0.001),明显证明了C6细胞凋亡的启动。 。此外,所有三组暴露6 h后,活性氧(ROS)显着增加(p <0.05; p <0.01和p <0.001),当共同处理T3细胞时,下降趋势(P <0.001)与N-乙酰半胱氨酸(NAC)。此外,通过用NAC处理C6细胞清除ROS诱导的氧化应激后,裂解的PARP的表达显着减弱(p <0.01),随后在G2 / M期细胞周期停滞减少(p <0.05)。 LAS诱导的细胞凋亡是由细胞内ROS介导的。因此,这些发现为包括体内研究在内的进一步研究提供了切实的基础,以揭示参与ROS介导的和LAS诱导的细胞毒性表现的分子机制。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere》 |2018年第8期|443-451|共9页
  • 作者单位

    Univ Lucknow, Dept Zool, Environm Toxicol & Bioremediat Lab, Lucknow 226007, Uttar Pradesh, India;

    Univ Lucknow, Dept Zool, Environm Toxicol & Bioremediat Lab, Lucknow 226007, Uttar Pradesh, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    C6 glioma cells; LAS; ROS; Apoptosis; Cell cycle arrest; PARP;

    机译:C6神经胶质瘤细胞;LAS;ROS;凋亡;细胞周期阻滞;PARP;

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