Wang Qian, Xie Yilin, Ma Shichao, Luo Hongliang, Qiu Yue
Department of Endocrinology and Metabolism, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, China.
School of Ophthalmology and Optometry, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Front Cell Dev Biol. 2024 Jul 29;12:1421191. doi: 10.3389/fcell.2024.1421191. eCollection 2024.
Approximately one-third of the patients with diabetes worldwide suffer from neuropathic pain, mainly categorized by spontaneous and stimulus-induced pain. Microglia are a class of immune effector cells residing in the central nervous system and play a pivotal role in diabetic neuropathic pain (DNP). Microglia specifically respond to hyperglycemia along with inflammatory cytokines and adenosine triphosphate produced during hyperglycemic damage to nerve fibers. Because of the presence of multiple receptors on the microglial surface, microglia are dynamically and highly responsive to their immediate environment. Following peripheral sensitization caused by hyperglycemia, microglia are affected by the cascade of inflammatory factors and other substances and respond accordingly, resulting in a change in their functional state for DNP pathogenesis. Inhibition of receptors such as P2X reporters, reducing cytokine expression levels in the microglial reactivity mechanisms, and inhibiting their intracellular signaling pathways can effectively alleviate DNP. A variety of drugs attenuate DNP by inhibiting the aforementioned processes induced by microglial reactivity. In this review, we summarize the pathological mechanisms by which microglia promote and maintain DNP, the drugs and therapeutic techniques available, and the latest advances in this field.
全球约三分之一的糖尿病患者患有神经病理性疼痛,主要分为自发性疼痛和刺激诱发性疼痛。小胶质细胞是一类存在于中枢神经系统的免疫效应细胞,在糖尿病性神经病理性疼痛(DNP)中起关键作用。小胶质细胞对高血糖以及高血糖损伤神经纤维过程中产生的炎性细胞因子和三磷酸腺苷有特异性反应。由于小胶质细胞表面存在多种受体,它们对周围环境具有动态且高度的反应性。在高血糖引起外周敏化后,小胶质细胞受到一系列炎性因子和其他物质的影响并做出相应反应,导致其功能状态发生变化,从而引发DNP发病机制。抑制P2X受体等,降低小胶质细胞反应性机制中的细胞因子表达水平,并抑制其细胞内信号通路,可有效缓解DNP。多种药物通过抑制小胶质细胞反应性诱导的上述过程来减轻DNP。在本综述中,我们总结了小胶质细胞促进和维持DNP的病理机制、可用的药物和治疗技术,以及该领域的最新进展。