神经科学
痛觉过敏
弥漫性有害抑制控制
刺激
伤害
抑制性突触后电位
有害刺激
刺激(心理学)
长时程增强
心理学
兴奋性突触后电位
总和
物理刺激
医学
内科学
受体
心理治疗师
作者
Ryan Patel,Joseph L. Taylor,Anthony H. Dickenson,Stephen B. McMahon,Kirsty Bannister
出处
期刊:Pain
[Ovid Technologies (Wolters Kluwer)]
日期:2024-01-09
卷期号:165 (9): 1978-1989
被引量:3
标识
DOI:10.1097/j.pain.0000000000003166
摘要
In humans and animals, high-frequency electrocutaneous stimulation (HFS) induces an "early long-term potentiation-like" sensitisation, where synaptic plasticity is underpinned by an ill-defined interaction between peripheral input and central modulatory processes. The relative contributions of these processes to the initial pain or nociceptive response likely differ from those that underpin development of the heightened response. To investigate the impact of HFS-induced hyperalgesia on pain and nociception in perception and neural terms, respectively, and to explore the impact of descending inhibitory pathway activation on the development of HFS-induced hyperalgesia, we performed parallel studies utilising identical stimuli to apply HFS concurrent to (1) a conditioned pain modulation paradigm during psychophysical testing in healthy humans or (2) a diffuse noxious inhibitory controls paradigm during in vivo electrophysiological recording of spinal neurones in healthy anaesthetised rats. High-frequency electrocutaneous stimulation alone induced enhanced perceptual responses to pinprick stimuli in cutaneous areas secondary to the area of electrical stimulation in humans and increased the excitability of spinal neurones which exhibited stimulus intensity-dependent coded responses to pinprick stimulation in a manner that tracked with human psychophysics, supporting their translational validity. Application of a distant noxious conditioning stimulus during HFS did not alter perceived primary or secondary hyperalgesia in humans or the development of primary or secondary neuronal hyperexcitability in rats compared with HFS alone, suggesting that, upon HFS-response initiation in a healthy nervous system, excitatory signalling escapes inhibitory control. Therefore, in this model, dampening facilitatory mechanisms rather than augmenting top-down inhibitions could prevent pain development.
科研通智能强力驱动
Strongly Powered by AbleSci AI