Glial cells as target for antidepressants in neuropathic pain

Q3 Medicine
Neuroforum Pub Date : 2022-03-24 DOI:10.1515/nf-2021-0036
Elisa Damo, Phillip Rieder, Ilknur Coban, Rangel Leal Silva, Frank Kirchhoff, Manuela Simonetti, Amit Agarwal
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引用次数: 1

Abstract

Abstract Several forms of chronic pain do not respond to the conventional analgesics, such as opioids, but can be treated with antidepressants, such as serotonin and noradrenalin reuptake inhibitors (SNRIs). Recent studies indicate that noradrenalin signalling is a key target for SNRI-induced analgesia in neuropathic pain. SNRIs inhibit chronic pain by blocking reuptake of noradrenalin and subsequent activation of adrenergic receptors on neurons in the dorsal horn of the spinal cord. However, in the nervous system, various subtypes of adrenergic receptors are highly expressed by astrocytes and microglial cells. Activation of these receptors on astrocytes engages complex intracellular signalling pathways and prevents inflammatory changes of microglia, which in turn can affect neuronal activity. Hence, SNRIs-induced modulations of the glial cell physiology can impact neural circuit functions and pain perception. In this review, we summarize our current knowledge on the impact of SNRIs on glial cells and in modulating chronic pain in experimental animal models.
神经胶质细胞作为抗抑郁药物治疗神经性疼痛的靶点
几种形式的慢性疼痛对阿片类药物等传统镇痛药没有反应,但可以用抗抑郁药治疗,如血清素和去甲肾上腺素再摄取抑制剂(SNRIs)。最近的研究表明,去甲肾上腺素信号是snri诱导的神经性疼痛镇痛的关键靶点。SNRIs通过阻断去甲肾上腺素的再摄取和随后脊髓背角神经元上肾上腺素能受体的激活来抑制慢性疼痛。然而,在神经系统中,各种亚型的肾上腺素能受体在星形胶质细胞和小胶质细胞中高度表达。星形胶质细胞上这些受体的激活参与了复杂的细胞内信号通路,并阻止了小胶质细胞的炎症变化,这反过来又可以影响神经元的活动。因此,snris诱导的神经胶质细胞生理调节可以影响神经回路功能和疼痛感知。在这篇综述中,我们总结了目前在实验动物模型中SNRIs对神经胶质细胞和慢性疼痛调节的影响方面的知识。
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来源期刊
Neuroforum
Neuroforum NEUROSCIENCES-
CiteScore
1.70
自引率
0.00%
发文量
30
期刊介绍: Neuroforum publishes invited review articles from all areas in neuroscience. Readership includes besides basic and medical neuroscientists also journalists, practicing physicians, school teachers and students. Neuroforum reports on all topics in neuroscience – from molecules to the neuronal networks, from synapses to bioethics.
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