越来越容易生气,几乎会流:炎症性疼痛中的TRPA1
Stephen B McMahon1, John N Wood
1London Pain Consortium, King's College London, London WC2R 2LS, United Kingdom. stephen.mcmahon@kcl.ac.uk
Cell
|March 28, 2006
概括
暂时受体潜在基林1 (TRPA1) 通道是感知催气和大等刺激物引起的炎症性疼痛的关键. 缺乏TRPA1的小鼠对机械和热刺激表现出正常的反应,这表明TRPA1在炎症性疼痛中起着特定的作用.
科学领域:
- 分子生物学分子生物学
- 神经科学是一个神经科学.
- 身体生理学 身体生理学
背景情况:
- 暂时受体潜力 (TRP) 阴离子通道对于感官转导至关重要.
- 这些通道检测机械,热和与疼痛相关的炎症信号.
- 在不同的感官模式中,TRP通道的特定作用仍在被阐明.
研究的目的:
- 研究TRPA1通道在疼痛感觉中的作用.
- 为了确定TRPA1是否参与对炎症媒介和刺激物的反应.
- 评估TRPA1在机械和热传感中的功能.
主要方法:
- 使用TRPA1缺乏的小鼠模型.
- 评估对各种刺激的行为反应,包括炎症媒介和刺激物.
- 测试了对机械和热刺激的感官感知.
主要成果:
- TRPA1在对内源性炎症媒介的疼痛反应中发挥着中心作用.
- TRPA1对于检测各种挥发性刺激物,如催气和大中的易挥发性刺激物至关重要.
- 缺乏TRPA1的小鼠表现出正常的机械和热传感,这表明它们具有特殊的功能.
结论:
- TRPA1通道特别参与炎症性疼痛信号传递.
- 对于正常的机械或热感觉来说,TRPA1不需要.
- TRPA1代表了炎症性疼痛条件的潜在治疗标.
相关概念视频
Thermosensation
Peripheral thermosensation is the perception of external temperature. A change in temperature (on the surface of the skin and other tissues) is detected by a family of temperature-sensitive ion channels called Transient Receptor Potential, or TRP, receptors. These receptors are located on free nerve endings. Those detecting cold temperatures are closer to the surface of the skin than the nerve endings detecting warmth. These thermoTRP channels, while temperature selective, have relatively...
Nociception
Nociception—the ability to feel pain—is essential for an organism’s survival and overall well-being. Noxious stimuli such as piercing pain from a sharp object, heat from an open flame, or contact with corrosive chemicals are first detected by sensory receptors, called nociceptors, located on nerve endings. Nociceptors express ion channels that convert noxious stimuli into electrical signals. When these signals reach the brain via sensory neurons, they are perceived as pain. Thus, pain helps the...
T Cell Types and Functions
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Acute Inflammation I: Inflammatory Response
Acute inflammation is a rapid, short-lived physiological response to tissue injury or infection, designed to eliminate harmful agents and initiate repair. This tightly regulated process typically lasts from minutes to several days and is triggered by factors such as microbial invasion, physical trauma, or chemical injury.Recognition and Mediator ReleaseThe inflammatory response begins when resident immune cells—such as mast cells, macrophages, and dendritic cells—detect damage-associated...
Acute Inflammation III: Local and Systemic Effects
Acute inflammation produces a coordinated set of local and systemic changes that limit injury, eliminate pathogens, and initiate repair. These responses arise within minutes of infection, trauma, or chemical insult and are driven by vascular alterations and leukocyte-derived mediators. When the stimulus resolves, the reaction typically abates within days.Local EffectsAt the site of injury, arteriolar vasodilation increases blood flow, resulting in redness and warmth. Simultaneously, increased...
Inflammatory Bowel Disease II: Ulcerative Colitis
Ulcerative colitis is a chronic inflammatory disorder of the colon characterized by continuous mucosal inflammation that typically begins in the rectum and extends proximally in a uniform pattern. Its pathogenesis involves a complex interplay of genetic predisposition, immune dysregulation, and environmental influences. These factors converge to impair the colon’s epithelial defenses and promote an exaggerated inflammatory response against luminal contents.Breakdown of the Mucosal BarrierA...


