红醇丰富的Magnolia officinalis树皮提取物减轻了创伤诱导的神经病痛
Vittoria Borgonetti1, Nicoletta Galeotti1
1Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA), Section of Pharmacology and Toxicology, University of Florence, Viale G. Pieraccini 6, 50139 Florence, Italy.
Antioxidants (Basel, Switzerland)
|August 26, 2023
概括
在神经病痛模型中,Magnolia officinalis提取物 (MOE) 和Honokiol (HNK) 显示了缓解疼痛的效果. 这些天然化合物减少神经炎症和氧化应激,为管理这种困难的疼痛状况提供了潜力.
科学领域:
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
- 自然产品化学 自然产品化学
背景情况:
- 神经病痛 (NP) 影响8%的人口,治疗选择有限.
- 氧化应激和神经炎症是慢性NP的关键因素.
- 天然抗氧化剂对NP管理有很大的前景.
研究的目的:
- 在神经病痛模型中研究一种富含荣基醇 (HNK) 的Magnolia officinalis提取物 (MOE) 的疗效.
- 探索MOE对神经炎症和氧化应激的影响背后的分子机制.
- 评估HNK对炎症反应的直接影响.
主要方法:
- 在NP.中利用了节省神经损伤 (SNI) 鼠标模型.
- 口服的MOE (30 mg/kg) 和评估的抗艾洛丁效应和运动运动活性.
- 对炎症标志物 (p-p38,p-JNK1,iNOS,p-p65,IL-1ß,IL-10,MBP,Nrf2) 和Notch通路组件 (Jagged1,NEXT) 的脊髓组织进行了分析.
- 研究了HNK对LPS刺激的BV2微质细胞的影响.
主要成果:
- 在SNI小鼠中,MOE表现出显著的抗氨酸效应,而不会导致发动机功能障碍.
- MOE降低了脊髓中神经炎症和氧化应激的关键标志物.
- MOE和HNK调节了Notch信号通路,并减少了促炎性细胞因子的产生.
- 影响部分由CB1受体相互作用介导.
结论:
- 在神经病痛疼痛模型中,MOE和HNK表现出显著的止痛特性.
- 这些化合物通过调节氧化应激,神经炎症和Notch信号通路来发挥作用.
- MOE和HNK代表了治疗神经病痛的有希望的自然疗法候选者.
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