Varrassi Giustino, Leoni Matteo Luigi Giuseppe, Farì Giacomo, Al-Alwany Ameen Abdulhasan, Al-Sharie Sarah, Fornasari Diego
Department of Research, Fondazione Paolo Procacci, 00193 Roma, Italy.
College of Medicine, University of Bagdad, Bagdad 10071, Iraq.
Cells. 2025 Aug 27;14(17):1320. doi: 10.3390/cells14171320.
Chronic pain is a complex and persistent condition involving sustained nociceptive input, maladaptive neuroplastic changes, and neuroimmune interactions. Central to its pathophysiology is the dysregulation of neuromodulatory signaling pathways, including neurotransmitters (e.g., dopamine, serotonin, norepinephrine), neuropeptides (e.g., substance P, CGRP), and neurotrophic factors (e.g., BDNF), which modulate both central and peripheral sensitization mechanisms. In disorders such as fibromyalgia, altered monoaminergic transmission has been implicated in the attenuation of descending inhibitory control, thereby enhancing pain perception and reducing responsiveness to conventional therapies. Concurrently, neuroinflammation, driven by glial cell activation and cytokine release, further exacerbates neuronal excitability and reinforces maladaptive signaling loops. Recent technological advances, including transcriptomic profiling, functional neuroimaging, and single-cell RNA sequencing, have provided new insights into patient-specific patterns of neuromodulatory dysfunction, highlighting potential biomarkers for disease stratification and therapeutic targeting. These developments support the hypothesis that dysregulated neuromodulatory circuits not only underlie diverse chronic pain phenotypes but may also serve as intervention points for precision medicine. This narrative review synthesizes current evidence on the roles of neuromodulatory systems in chronic pain, focusing on synaptic plasticity, nociceptor sensitization, and neuroimmune crosstalk. By integrating preclinical findings with clinical observations, we propose a mechanistic framework for understanding pain chronification and guiding future therapeutic strategies. Harnessing neuromodulatory targets, whether pharmacologically or via neuromodulation technologies, could offer more personalized and effective approaches to chronic pain management.
慢性疼痛是一种复杂且持续的病症,涉及持续的伤害性感受输入、适应性不良的神经可塑性变化以及神经免疫相互作用。其病理生理学的核心是神经调节信号通路的失调,包括神经递质(如多巴胺、5-羟色胺、去甲肾上腺素)、神经肽(如P物质、降钙素基因相关肽)和神经营养因子(如脑源性神经营养因子),这些物质调节中枢和外周敏化机制。在纤维肌痛等疾病中,单胺能传递的改变与下行抑制控制的减弱有关,从而增强疼痛感知并降低对传统疗法的反应性。同时,由胶质细胞激活和细胞因子释放驱动的神经炎症进一步加剧神经元兴奋性并强化适应性不良的信号回路。最近的技术进步,包括转录组分析、功能神经成像和单细胞RNA测序, 为神经调节功能障碍的患者特异性模式提供了新的见解,突出了疾病分层和治疗靶点的潜在生物标志物。这些进展支持了这样一种假设,即失调的神经调节回路不仅是多种慢性疼痛表型的基础,而且还可能作为精准医学的干预点。这篇叙述性综述综合了关于神经调节系统在慢性疼痛中作用的当前证据,重点关注突触可塑性、伤害感受器敏化和神经免疫串扰。通过将临床前研究结果与临床观察相结合,我们提出了一个理解疼痛慢性化和指导未来治疗策略的机制框架。利用神经调节靶点,无论是通过药理学还是通过神经调节技术,都可以为慢性疼痛管理提供更个性化和有效的方法。