Silva Rafaela V, Oliveira Julia T, Santos Bruna L R, Dias Fabiana C, Martinez Ana M B, Lima Cleverton K F, Miranda Ana L P
Laboratório de Estudos em Farmacologia Experimental, Departamento de Biotecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Laboratório de Neurodegeneração e Reparo, Departamento de Patologia, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Front Pharmacol. 2017 Oct 17;8:723. doi: 10.3389/fphar.2017.00723. eCollection 2017.
Fish oil (FO) is the main source of long chain omega-3 polyunsaturated fatty acids (ω-3 PUFAs), which display relevant analgesic and anti-inflammatory properties. Peripheral nerve injury is driven by degeneration, neuroinflammation, and neuronal plasticity which results in neuropathic pain (NP) symptoms such as allodynia and hyperalgesia. We tested the preventive effect of an EPA/DHA-concentrate fish oil (CFO) on NP development and regenerative features. Swiss mice received daily oral treatment with CFO 4.6 or 2.3 g/kg for 10 days after NP was induced by partial sciatic nerve ligation. Mechanical allodynia and thermal hypernociception were assessed 5 days after injury. CFO 2.3 g/kg significantly prevented mechanical and thermal sensitization, reduced TNF levels in the spinal cord, sciatic MPO activity, and ATF-3 expression on DRG cells. CFO improved Sciatic Functional Index (SFI) as well as electrophysiological recordings, corroborating the increased GAP43 expression and total number of myelinated fibers observed in sciatic nerve. No locomotor activity impairment was observed in CFO treated groups. These results point to the regenerative and possibly protective properties of a combined EPA and DHA oral administration after peripheral nerve injury, as well as its anti-neuroinflammatory activity, evidencing ω-3 PUFAs promising therapeutic outcomes for NP treatment.
鱼油(FO)是长链ω-3多不饱和脂肪酸(ω-3 PUFAs)的主要来源,这些脂肪酸具有相关的镇痛和抗炎特性。周围神经损伤由退变、神经炎症和神经元可塑性驱动,会导致神经性疼痛(NP)症状,如痛觉过敏和异常性疼痛。我们测试了一种富含二十碳五烯酸/二十二碳六烯酸的浓缩鱼油(CFO)对NP发展和再生特征的预防作用。在通过部分坐骨神经结扎诱导NP后,瑞士小鼠每天口服4.6或2.3 g/kg的CFO,持续10天。在损伤后5天评估机械性痛觉过敏和热痛觉过敏。2.3 g/kg的CFO显著预防了机械性和热敏化,降低了脊髓中的肿瘤坏死因子水平、坐骨神经的髓过氧化物酶活性以及背根神经节细胞上的活化转录因子3(ATF-3)表达。CFO改善了坐骨神经功能指数(SFI)以及电生理记录,证实了坐骨神经中观察到的生长相关蛋白43(GAP43)表达增加和有髓纤维总数增加。在CFO治疗组中未观察到运动活动受损。这些结果表明,外周神经损伤后联合口服二十碳五烯酸和二十二碳六烯酸具有再生作用,可能还具有保护作用,以及其抗神经炎症活性,证明ω-3 PUFAs在NP治疗方面有良好的治疗前景。