Departamento de Biomedicina-Unidade de Farmacologia e Terapêutica, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Centro de Investigação Farmacológica e Inovação Medicamentosa (MedInUP), Universidade do Porto, Porto, Portugal.
PLoS One. 2023 Jun 22;18(6):e0287392. doi: 10.1371/journal.pone.0287392. eCollection 2023.
Specialized pro-resolving mediators (SPMs) have recently emerged as promising therapeutic approaches for neuropathic pain (NP). We evaluated the effects of oral treatment with the SPM Maresin 1 (MaR1) on behavioral pain responses and spinal neuroinflammation in male and female C57BL/6J mice with spared nerve injury (SNI)-induced NP. MaR1, or vehicle, was administered once daily, on post-surgical days 3 to 5, by voluntary oral intake. Sensory-discriminative and affective-motivational components of pain were evaluated with von Frey and place escape/avoidance paradigm (PEAP) tests, respectively. Spinal microglial and astrocytic activation were assessed by immunofluorescence, and the spinal concentration of cytokines IL-1β, IL-6, IL-10, and macrophage colony-stimulating factor (M-CSF) were evaluated by multiplex immunoassay. MaR1 treatment reduced SNI-induced mechanical hypersensitivity on days 7 and 11 in both male and female mice, and appeared to ameliorate the affective component of pain in males on day 11. No definitive conclusions could be drawn about the impact of MaR1 on the affective-motivational aspects of pain in female mice, since repeated suprathreshold mechanical stimulation of the affected paw in the dark compartment did not increase the preference of vehicle-treated SNI females for the light side, during the PEAP test session (a fundamental assumption for PAEP's validity). MaR1 treatment also reduced ipsilateral spinal microglial and astrocytic activation in both sexes and marginally increased M-CSF in males, while not affecting cytokines IL-1β, IL-6 and IL-10 in either sex. In summary, our study has shown that oral treatment with MaR1 (i) produces antinociception even in an already installed peripheral NP mouse model, and (ii) this antinociception may extend for several days beyond the treatment time-frame. These therapeutic effects are associated with attenuated microglial and astrocytic activation in both sexes, and possibly involve modulation of M-CSF action in males.
特殊的促解决介质 (SPM) 最近作为治疗神经性疼痛 (NP) 的有前途的方法出现。我们评估了口服治疗 SPM maresin 1 (MaR1) 对雄性和雌性 C57BL/6J 小鼠神经损伤 (SNI) 引起的 NP 后行为疼痛反应和脊髓神经炎症的影响。MaR1 或载体在手术后第 3 至 5 天每天通过自愿口服给药一次。使用 von Frey 和位置逃避/回避范式 (PEAP) 测试分别评估疼痛的感觉-辨别和情感-动机成分。通过免疫荧光评估脊髓小胶质细胞和星形胶质细胞的激活,通过多重免疫测定评估脊髓细胞因子 IL-1β、IL-6、IL-10 和巨噬细胞集落刺激因子 (M-CSF) 的浓度。MaR1 治疗减少了 SNI 在雄性和雌性小鼠的第 7 天和第 11 天引起的机械性超敏反应,并在第 11 天似乎改善了雄性疼痛的情感成分。由于在 PEAP 测试过程中,对黑暗隔间中受影响的爪子进行重复的超阈值机械刺激并没有增加接受载体治疗的 SNI 雌性对光侧的偏好,因此无法对 MaR1 对雌性小鼠疼痛的情感-动机方面的影响得出明确的结论。MaR1 治疗还减少了两性的同侧脊髓小胶质细胞和星形胶质细胞的激活,并在雄性中轻微增加了 M-CSF,而对两性的细胞因子 IL-1β、IL-6 和 IL-10 没有影响。总之,我们的研究表明,口服 MaR1 治疗 (i) 即使在已经建立的周围 NP 小鼠模型中也能产生镇痛作用,并且 (ii) 这种镇痛作用可能会在治疗时间框架之外持续数天。这些治疗效果与两性中小胶质细胞和星形胶质细胞的激活减弱有关,并且可能涉及雄性中 M-CSF 作用的调节。