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百里醌对过氧亚硝酸盐诱导的组蛋白 H2A 修饰的保护作用:体外研究。

Protective potential of thymoquinone against peroxynitrite induced modifications in histone H2A: In vitro studies.

机构信息

College of Medicine, Qassim University, Buraidah, Saudi Arabia.

College of Medicine, Qassim University, Buraidah, Saudi Arabia.

出版信息

Int J Biol Macromol. 2018 Jun;112:169-174. doi: 10.1016/j.ijbiomac.2018.01.157. Epub 2018 Feb 26.

Abstract

Peroxynitrite (ONOO) is a reactive oxidant involved in numerous pathological conditions. Thymoquinone (TQ) is an active constituent of Nigella sativa and is reported to have anti-disease activities, but its role on ONOO has never been investigated. This study was undertaken to investigate the role of TQ on ONOO-induced damage of histone-H2A. Our novel data showed TQ significantly inhibited ONOO-induced oxidative damage in histone-H2A. ONOO induces UV-hypochromicity of histone-H2A, whereas TQ reversed this effect to hyperchromicity. Tyrosine fluorescence was significantly reduced by ONOO and was significantly increased upon TQ treatment. TQ reduces ONOO-induced hydrophobicity in histone-H2A and also reduces thermal stability of ONOO-histone H2A complex. SDS-PAGE of native histone-H2A showed a single band, which disappeared when treated with ONOO alone. This changed was retained when protein samples were treated with TQ. Similar protective effects of TQ were found when protein carbonyl contents were estimated. In conclusion, this is the first study that shows the potential of TQ against ONOO-induced damaged of histone-H2A. TQ inhibits oxidative modification of tyrosine, lysine, arginine, proline and threonine in histone-H2A. These results have importance for the development of novel therapeutic strategies for the treatment of disorders, where ONOO plays a role.

摘要

过氧亚硝酸盐 (ONOO) 是一种参与多种病理状况的反应性氧化剂。百里醌 (TQ) 是黑种草的一种活性成分,据报道具有抗疾病活性,但它对 ONOO 的作用从未被研究过。本研究旨在研究 TQ 对 ONOO 诱导的组蛋白-H2A 损伤的作用。我们的新数据表明,TQ 可显著抑制 ONOO 诱导的组蛋白-H2A 氧化损伤。ONOO 诱导组蛋白-H2A 的 UV 减色性,而 TQ 逆转了这种超色性。酪氨酸荧光被 ONOO 显著降低,而 TQ 处理后显著增加。TQ 降低 ONOO 诱导的组蛋白-H2A 疏水性,并降低 ONOO-组蛋白 H2A 复合物的热稳定性。天然组蛋白-H2A 的 SDS-PAGE 显示出单一条带,当单独用 ONOO 处理时,该条带消失。当用 TQ 处理蛋白质样品时,这种变化得以保留。当估计蛋白质羰基含量时,发现 TQ 具有相似的保护作用。总之,这是第一项表明 TQ 具有对抗 ONOO 诱导的组蛋白-H2A 损伤的潜力的研究。TQ 抑制组蛋白-H2A 中酪氨酸、赖氨酸、精氨酸、脯氨酸和苏氨酸的氧化修饰。这些结果对于开发治疗 ONOO 发挥作用的疾病的新型治疗策略具有重要意义。

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