Molecular Pharmacology, Department of Biofunctional Evaluation, Gifu Pharmaceutical University, 1-25-4 Daigakunishi, Gifu, 501-1196, Japan.
Department of Clinical Research, National Hospital Organization, Nagara Medical Center, Gifu, 502-8558, Japan.
Neurochem Res. 2018 Jul;43(7):1413-1423. doi: 10.1007/s11064-018-2556-1. Epub 2018 May 24.
Maresin 1 is a novel pro-resolving mediator derived from docosahexaenoic acid (DHA), with potent anti-inflammation effects against several animal models, including brain ischemia, sepsis, and lung fibrosis. However, its effect against motor neuron cell death is still not investigated. Therefore, we investigated the effects of maresin 1 on several stress-induced motor neuron cell death. Maresin 1 suppressed combinatorial stress which was evoked by superoxide dismutase 1 (SOD1) and serum-free, -induced motor neuron cells death in a concentration-dependent manner, and had a stronger neuroprotective effective than DHA. Maresin 1 also had neuroprotective effects against transactivation response DNA-binding protein (TDP)-43 and serum-free stress, HO, and tunicamycin-induced cell death. Maresin 1 reduced the reactive oxygen species (ROS) production caused by SOD1 or TDP-43. Moreover, maresin 1 suppressed the NF-κB activation induced by SOD1 and serum-free stress. These data indicate that maresin 1 has motor neuron protective effects against several stresses by reduction of ROS production or attenuation of the NF-κB activation. Maresin 1 also had neuroprotective effects against HO, and tunicamycin-induced cell death in a concentration-dependent manner. Finally, maresin 1 ameliorated the motor function deficits of spinal muscular atrophy model in which endoplasmic reticulum stress was upregulated. Thus, maresin 1 may be beneficial to protect against motor neuron diseases.
maresin 1 是一种新型的二十二碳六烯酸(DHA)衍生的促解决介质,具有强大的抗炎作用,可对抗几种动物模型,包括脑缺血、败血症和肺纤维化。然而,其对运动神经元细胞死亡的影响仍未被研究。因此,我们研究了maresin 1 对几种应激诱导的运动神经元细胞死亡的影响。maresin 1 以浓度依赖性方式抑制由超氧化物歧化酶 1(SOD1)和无血清诱导的组合应激诱导的运动神经元细胞死亡,并且比 DHA 具有更强的神经保护作用。maresin 1 还对转激活反应 DNA 结合蛋白(TDP-43)和无血清应激、HO 和衣霉素诱导的细胞死亡具有神经保护作用。maresin 1 减少了由 SOD1 或 TDP-43 引起的活性氧(ROS)的产生。此外,maresin 1 抑制了由 SOD1 和无血清应激诱导的 NF-κB 激活。这些数据表明,maresin 1 通过减少 ROS 产生或减弱 NF-κB 激活,对几种应激具有运动神经元保护作用。maresin 1 还以浓度依赖性方式对 HO 和衣霉素诱导的细胞死亡具有神经保护作用。最后,maresin 1 改善了内质网应激上调的脊髓性肌萎缩症模型的运动功能缺陷。因此,maresin 1 可能有益于预防运动神经元疾病。