Research Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, Girona, Spain.
Department of Anatomy, Division of Neuroanatomy, Faculty of Medicine, Masaryk University, Brno, Czechia.
Sci Rep. 2022 Sep 2;12(1):14980. doi: 10.1038/s41598-022-19109-4.
More than half of spinal cord injury (SCI) patients develop central neuropathic pain (CNP), which is largely refractory to current treatments. Considering the preclinical evidence showing that polyphenolic compounds may exert antinociceptive effects, the present work aimed to study preventive effects on SCI-induced CNP development by repeated administration of two vegetal polyphenolic extracts: grape stalk extract (GSE) and coffee extract (CE). Thermal hyperalgesia and mechanical allodynia were evaluated at 7, 14 and 21 days postinjury. Then, gliosis, ERK phosphorylation and the expression of CCL2 and CX3CL1 chemokines and their receptors, CCR2 and CX3CR1, were analyzed in the spinal cord. Gliosis and CX3CL1/CX3CR1 expression were also analyzed in the anterior cingulate cortex (ACC) and periaqueductal gray matter (PAG) since they are supraspinal structures involved in pain perception and modulation. GSE and CE treatments modulated pain behaviors accompanied by reduced gliosis in the spinal cord and both treatments modulated neuron-glia crosstalk-related biomolecules expression. Moreover, both extracts attenuated astrogliosis in the ACC and PAG as well as microgliosis in the ACC with an increased M2 subpopulation of microglial cells in the PAG. Finally, GSE and CE prevented CX3CL1/CX3CR1 upregulation in the PAG, and modulated their expression in ACC. These findings suggest that repeated administrations of either GSE or CE after SCI may be suitable pharmacologic strategies to attenuate SCI-induced CNP development by means of spinal and supraspinal neuroinflammation modulation.
超过一半的脊髓损伤 (SCI) 患者会出现中枢神经性疼痛 (CNP),而目前的治疗方法对此类疼痛大多效果不佳。鉴于临床前证据表明多酚化合物可能具有镇痛作用,本研究旨在通过重复给予两种植物多酚提取物——葡萄茎提取物 (GSE) 和咖啡提取物 (CE),研究其对 SCI 诱导的 CNP 发展的预防作用。在损伤后 7、14 和 21 天评估热痛觉过敏和机械性痛觉过敏。然后,分析脊髓中的神经胶质增生、ERK 磷酸化以及趋化因子 CCL2 和 CX3CL1 及其受体 CCR2 和 CX3CR1 的表达。由于在前扣带回皮层 (ACC) 和中脑导水管周围灰质 (PAG) 中存在与疼痛感知和调节相关的超脊髓结构,因此还分析了这两个区域的神经胶质增生和 CX3CL1/CX3CR1 的表达。GSE 和 CE 治疗可调节疼痛行为,同时减少脊髓中的神经胶质增生,两种治疗方法还可调节与神经元-神经胶质细胞相互作用相关的生物分子表达。此外,两种提取物均可减轻 ACC 中的星形胶质细胞增生和 PAG 中的小胶质细胞增生,并增加 PAG 中小胶质细胞 M2 亚群的数量。最后,GSE 和 CE 可防止 PAG 中 CX3CL1/CX3CR1 的上调,并调节其在 ACC 中的表达。这些发现表明,SCI 后重复给予 GSE 或 CE 可能是一种合适的药物治疗策略,可通过调节脊髓和中枢神经系统的神经炎症来减轻 SCI 诱导的 CNP 发展。