在老鼠中,内活性氧物种通过TRPA1调解炎症性疼痛和过敏症
Youping Zhang1, Jamila Asgar1, Huizhong Shou1
1Department of Neural and Pain Sciences, University of Maryland School of Dentistry, Baltimore, MD, United States.
Frontiers in pain research (Lausanne, Switzerland)
|June 16, 2023
概括
周围炎症增加了三腺 (TG) 中的活性氧物种 (ROS),导致疼痛过敏. 减少ROS或阻断TG中的TRPA1通道可以缓解这种炎症性疼痛.
科学领域:
- 神经科学是一个神经科学.
- 疼痛研究 疼痛研究
- 细胞生物学 细胞生物学
背景情况:
- 反应性氧物种 (ROS) 在疼痛途径中发挥作用.
- 在炎症性疼痛期间,ROS在感觉质中的功能尚不清楚.
研究的目的:
- 为了确定外周炎症是否会导致长时间的ROS积聚在三角关节 (TG) 中.
- 通过TRPA1激活来调查内ROS是否会通过TRPA1激活调解疼痛过敏.
- 为了检查ROS是否在炎症期间在TG上调TRPA1表达.
主要方法:
- 诱导周围炎症和评估机械过敏症.
- 在TG中测量ROS水平.
- 在TG中进行ROS的药理清除和TRPA1的阻断.
- 在TG中TRPA1表达的评估.
主要成果:
- 周围炎症导致TG在高峰超症期间的ROS产量增加.
- 清除ROS或阻断TG中的TRPA1可以减少炎症性过敏症.
- 在TG中外源性ROS通过TRPA1.1诱导过敏症和疼痛类行为.
- 内ROS增加了TG中的TRPA1表达.
结论:
- 在TG中的ROS积累有助于以TRPA1依赖的方式导致炎症性疼痛和过敏症.
- 通过上调TRPA1表达,ROS会加剧疼痛.
- 针对质性ROS的治疗可以缓解炎症性疼痛.
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