Department of Neurosurgery, Chang Gung Memorial Hospital, Linkou, Chang Gung University School of Medicine, Kwei-San, Taoyuan 33305, Taiwan.
Department of Chemical and Materials and Materials Engineering, Chang Gung University, Kwei-San, Taoyuan 33302, Taiwan.
Int J Mol Sci. 2020 Sep 24;21(19):7031. doi: 10.3390/ijms21197031.
Spinal cord injury (SCI) is associated with disability and a drastic decrease in quality of life for affected individuals. Previous studies support the idea that docosahexaenoic acid (DHA)-based pharmacological approach is a promising therapeutic strategy for the management of acute SCI. We postulated that a nanostructured material for controlled delivery of DHA at the lesion site may be well suited for this purpose. Toward this end, we prepare drug-loaded fibrous mats made of core-shell nanofibers by electrospinning, which contained a polylactic acid (PLA) shell for encapsulation of DHA within the core, for delivery of DHA in situ. In vitro study confirmed sustained DHA release from PLA/DHA core-shell nanofiber membrane (CSNM) for up to 36 days, which could significantly increase neurite outgrowth from primary cortical neurons in 3 days. This is supported by the upregulation of brain-derived neurotropic factor (BDNF) and neurotrophin-3 (NT-3) neural marker genes from qRT-PCR analysis. Most importantly, the sustained release of DHA could significantly increase the neurite outgrowth length from cortical neuron cells in 7 days when co-cultured with PLA/DHA CSNM, compared with cells cultured with 3 μM DHA. From in vivo study with a SCI model created in rats, implantation of PLA/DHA CSNM could significantly improve neurological functions revealed by behavior assessment in comparison with the control (no treatment) and the PLA CSNM groups. According to histological analysis, PLA/DHA CSNM also effectively reduced neuron loss and increased serotonergic nerve sprouting. Taken together, the PLA/DHA CSNM may provide a nanostructured drug delivery system for DHA and contribute to neuroprotection and promoting neuroplasticity change following SCI.
脊髓损伤 (SCI) 会导致残疾,并极大地降低患者的生活质量。先前的研究支持这样一种观点,即基于二十二碳六烯酸 (DHA) 的药物治疗方法是治疗急性 SCI 的一种有前途的治疗策略。我们推测,在病变部位控制释放 DHA 的纳米结构材料可能非常适合这种用途。为此,我们通过静电纺丝制备了载药纤维垫,由核壳纳米纤维组成,其中包含聚乳酸 (PLA) 壳,用于将 DHA 封装在核内,以便原位递送 DHA。体外研究证实 PLA/DHA 核壳纳米纤维膜 (CSNM) 可长达 36 天持续释放 DHA,这可以显著增加原代皮质神经元的神经突生长 3 天。这得到了 qRT-PCR 分析中脑源性神经营养因子 (BDNF) 和神经营养因子-3 (NT-3) 神经标记基因上调的支持。最重要的是,与单独培养的细胞相比,在与 PLA/DHA CSNM 共培养 7 天时,持续释放的 DHA 可以显著增加皮质神经元细胞的神经突生长长度,细胞中 DHA 浓度为 3 μM。在大鼠 SCI 模型的体内研究中,与对照组(无治疗)和 PLA CSNM 组相比,PLA/DHA CSNM 的植入可显著改善行为评估中揭示的神经功能。根据组织学分析,PLA/DHA CSNM 还可以有效减少神经元丢失并增加 5-羟色胺能神经突生长。综上所述,PLA/DHA CSNM 可为 DHA 提供纳米结构药物递送系统,并有助于 SCI 后的神经保护和促进神经可塑性变化。