Puopolo Michelino
Department of Anesthesiology, Stony Brook Medicine, Stony Brook, NY, USA.
Neural Regen Res. 2019 Jun;14(6):925-930. doi: 10.4103/1673-5374.250567.
Nociceptive signals conveyed to the dorsal horn of the spinal cord by primary nociceptors are subject to extensive modulation by local neurons and by supraspinal descending pathways to the spinal cord before being relayed to higher brain centers. Descending modulatory pathways to the spinal cord comprise, among others, noradrenergic, serotonergic, γ-aminobutyric acid (GABA)ergic, and dopaminergic fibers. The contributions of noradrenaline, serotonin, and GABA to pain modulation have been extensively investigated. In contrast, the contributions of dopamine to pain modulation remain poorly understood. The focus of this review is to summarize the current knowledge of the contributions of dopamine to pain modulation. Hypothalamic A11 dopaminergic neurons project to all levels of the spinal cord and provide the main source of spinal dopamine. Dopamine receptors are expressed in primary nociceptors as well as in spinal neurons located in different laminae in the dorsal horn of the spinal cord, suggesting that dopamine can modulate pain signals by acting at both presynaptic and postsynaptic targets. Here, I will review the literature on the effects of dopamine and dopamine receptor agonists/antagonists on the excitability of primary nociceptors, the effects of dopamine on the synaptic transmission between primary nociceptors and dorsal horn neurons, and the effects of dopamine on pain in rodents. Published data support both anti-nociceptive effects of dopamine mediated by D2-like receptors and pro-nociceptive effects mediated by D1-like receptors.
由初级伤害感受器传递至脊髓背角的伤害性信号,在被中继至更高脑区之前,会受到局部神经元以及脊髓上下行通路的广泛调制。脊髓上的下行调制通路包括去甲肾上腺素能、5-羟色胺能、γ-氨基丁酸(GABA)能和多巴胺能纤维等。去甲肾上腺素、5-羟色胺和GABA对疼痛调制的作用已得到广泛研究。相比之下,多巴胺对疼痛调制的作用仍知之甚少。本综述的重点是总结当前关于多巴胺对疼痛调制作用的知识。下丘脑A11多巴胺能神经元投射至脊髓的各级水平,并提供脊髓多巴胺的主要来源。多巴胺受体在初级伤害感受器以及脊髓背角不同板层的脊髓神经元中均有表达,这表明多巴胺可通过作用于突触前和突触后靶点来调制疼痛信号。在此,我将综述关于多巴胺和多巴胺受体激动剂/拮抗剂对初级伤害感受器兴奋性的影响、多巴胺对初级伤害感受器与背角神经元之间突触传递的影响,以及多巴胺对啮齿动物疼痛的影响的文献。已发表的数据支持由D2样受体介导的多巴胺的抗伤害感受作用以及由D1样受体介导的促伤害感受作用。