Mathew Sharon, Ashraf Sadaf, Shorter Susan, Tozzi Gianluca, Koutsikou Stella, Ovsepian Saak V
Faculty of Engineering and Science, University of Greenwich London, Chatham Maritime, Kent, UK.
Medway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, Kent, UK.
Neuroscientist. 2024 Dec 12;31(4):10738584241293049. doi: 10.1177/10738584241293049.
Swelling, stiffness, and pain in synovial joints are primary hallmarks of osteoarthritis and rheumatoid arthritis. Hyperactivity of nociceptors and excessive release of inflammatory factors and pain mediators play a crucial role, with emerging data suggesting extensive remodelling and plasticity of joint innervations. Herein, we review structural, functional, and molecular alterations in sensory and autonomic axons wiring arthritic joints and revisit mechanisms implicated in the sensitization of nociceptors, leading to chronic pain. Sprouting and reorganization of sensory and autonomic fibers with the invasion of ectopic branches into surrounding inflamed tissues are associated with the upregulation of pain markers. These changes are frequently complemented by a phenotypic switch of sensory and autonomic profiles and activation of silent axons, inferring homeostatic adjustments and reprogramming of innervations. Identifying critical molecular players and neurobiological mechanisms underpinning the rewiring and sensitization of joints is likely to elucidate causatives of neuroinflammation and chronic pain, assisting in finding new therapeutic targets and opportunities for interventions.
滑膜关节的肿胀、僵硬和疼痛是骨关节炎和类风湿性关节炎的主要特征。伤害感受器的过度活跃以及炎症因子和疼痛介质的过度释放起着关键作用,最新数据表明关节神经支配存在广泛的重塑和可塑性。在此,我们综述了感觉和自主神经轴突连接关节炎关节时的结构、功能和分子改变,并重新审视了与伤害感受器敏化相关的机制,这些机制会导致慢性疼痛。感觉和自主神经纤维的发芽和重组,以及异位分支侵入周围炎症组织,与疼痛标志物的上调有关。这些变化常常伴随着感觉和自主神经表型的转换以及沉默轴突的激活,这意味着神经支配的稳态调整和重新编程。确定关节重新布线和敏化背后的关键分子参与者和神经生物学机制,可能会阐明神经炎症和慢性疼痛的病因,有助于找到新的治疗靶点和干预机会。