在偏头痛患者中对Nrf2/Keap1通路的评估
Fatih Koçtürk1, Firdevs Emekli2, Kadir Eği2
1Department of Neurology, Faculty of Medicine, Kahramanmaras Sutcu Imam University, 46040 Kahramanmaras, Turkey.
Medicina (Kaunas, Lithuania)
|October 29, 2025
概括
氧化应激和核因素红色素2相关因子2 (Nrf2) /凯尔赫类ECH相关蛋白1 (Keap1) 途径在偏头痛中至关重要. 较低的Nrf2和较高的Keap1表明抗氧化剂防御不足,这表明这种途径是潜在的偏头痛治疗目标.
科学领域:
- 神经学 神经学
- 生物化学 生物化学
- 病理生理学 病理生理学
背景情况:
- 偏头痛是一种流行的神经系统疾病,影响生活质量.
- 它的发病包括三角神经血管激活,神经性炎症和氧化应激.
研究的目的:
- 为了研究核因子红色素2相关因子2 (Nrf2) /凯尔奇类ECH相关蛋白1 (Keap1) 途径在偏头痛发病过程中的作用.
- 评估偏头痛患者的氧化应激标志物.
主要方法:
- 氧化应激参数的分析:总氧化剂水平 (TOS),总抗氧化剂水平 (TAS) 和氧化应激指数 (OSI).
- 对Nrf2/Keap1信号通路组件的评估.
- 测量氧化LDL (oxLDL) 和GSK3B水平.
主要成果:
- 与对照人群相比,偏头痛患者的Keap1水平显著提高,Nrf2和TAS水平降低.
- 增加的oxLDL和GSK3B证实了氧化应激负担的增加.
- 显著更高的OSI值表明偏头痛患者的系统氧化失衡.
结论:
- 氧化应激和Nrf2/Keap1通路是偏头痛病原体的组成部分.
- 降低Nrf2活性和升高Keap1表明偏头痛中抗氧化剂防御受损.
- 针对Nrf2/Keap1通路并减少氧化应激可能提供新的偏头痛治疗策略.
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