Neuropathic pain, antidepressant drugs, and inflammation: a narrative review.

Giulia Catalisano, Gioacchina Martina Campione, Giulia Spurio, Alberto Nicolò Galvano, Cesira Palmeri di Villalba, Antonino Giarratano, Antonietta Alongi, Mariachiara Ippolito, Andrea Cortegiani
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Abstract

Background: Neuropathic pain (NP) is a chronic and disabling condition, caused by a lesion or disease of the somatosensory nervous system, characterized by a systemic inflammatory state. Signs and associated symptoms are rarely recognized, and response to usual analgesic drugs is poor. Antidepressant drugs are first-line agents for the treatment of NP. This narrative review aims to summarize the role of antidepressant drugs in treating NP and their mechanism of action, focusing on the effects on inflammatory cytokines.

Main text: Peripheral nerve injury leads to a local inflammatory response and to the disruption of the blood-medullary barrier, allowing the influx of peripheral immune cells into the central nervous system. Antidepressants have antinociceptive effects because they recruit long-term neuronal plasticity. Amitriptyline modulates the inflammatory response due to the reduction of the mRNA of pro-inflammatory cytokines acting as an adenosine agonist and leading to the activation of the A3AR receptor. Through toll-like receptors, local inflammation determines the release of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) that drives and stimulates the hyperflammation in NP. Nortriptyline has an important antiallodynic effect in NP as it determines the recruitment of norepinephrine in the dorsal root ganglia. By modulating the β2-adrenoreceptors expressed by non-neuronal satellite cells, it inhibits the local production of TNF-α and determines a reduction of NP symptoms. Following the administration of antidepressants, there is a reduction in the production of TNF-α in the brain which in turn transforms the function of the α2-adrenergic receptor from an inhibitor to an activator of the release of norepinephrine. This is important to prevent the development of chronic pain.

Conclusion: Inflammatory cytokines are the main players in a bidirectional communication between the central and peripheral nervous system and the immune system in NP. Antidepressants have an important role in NP. Further research should explore the interaction between neuroinflammation in NP, the effects of antidepressants and the clinical relevance of this interaction.

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神经性疼痛、抗抑郁药物和炎症:叙述性综述。
背景:神经病理性疼痛(NP)是一种慢性致残性疾病,由躯体感觉神经系统的病变或疾病引起,以全身炎症状态为特征。其体征和相关症状很少被察觉,对常用镇痛药物的反应也很差。抗抑郁药物是治疗 NP 的一线药物。这篇叙述性综述旨在总结抗抑郁药物在治疗 NP 中的作用及其作用机制,重点是对炎症细胞因子的影响:外周神经损伤导致局部炎症反应和血髓屏障破坏,使外周免疫细胞涌入中枢神经系统。抗抑郁药具有抗痛觉作用,因为它们能促进神经元的长期可塑性。阿米替林作为一种腺苷激动剂,可减少促炎细胞因子的 mRNA,从而激活 A3AR 受体,从而调节炎症反应。通过收费样受体,局部炎症决定了肿瘤坏死因子-α(TNF-α)等促炎细胞因子的释放,从而推动和刺激 NP 的炎症亢进。去甲替林对 NP 有重要的镇痛作用,因为它决定了去甲肾上腺素在背根神经节中的募集。通过调节非神经元卫星细胞表达的 β2-肾上腺素受体,它能抑制 TNF-α 在局部的产生,从而减轻 NP 症状。服用抗抑郁药后,大脑中 TNF-α 的分泌会减少,这反过来又会使α2-肾上腺素能受体的功能从去甲肾上腺素释放的抑制剂转变为激活剂。这对于预防慢性疼痛的发生非常重要:炎性细胞因子是 NP 中枢神经系统、外周神经系统和免疫系统之间双向交流的主要参与者。抗抑郁药在 NP 中发挥着重要作用。进一步的研究应探讨 NP 中神经炎症、抗抑郁药的作用以及这种相互作用的临床意义之间的相互作用。
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