Hong Yunkyung, Jin Yunho, Park Kanghui, Choi Jeonghyun, Kang Hyunbon, Lee Sang-Rae, Hong Yonggeun
Department of Physical Therapy, College of Healthcare Medical Science & Engineering, Inje University, Gimhae 50834, Korea.
Department of Rehabilitation Science, Graduate School of Inje University, Gimhae 50834, Korea.
J Clin Med. 2019 Jan 23;8(2):135. doi: 10.3390/jcm8020135.
We investigated the effects of environmental lighting conditions regulating endogenous melatonin production on neural repair, following experimental spinal cord injury (SCI). Rats were divided into three groups randomly: the SCI + L/D (12/12-h light/dark), SCI + LL (24-h constant light), and SCI + DD (24-h constant dark) groups. Controlled light/dark cycle was pre-applied 2 weeks before induction of spinal cord injury. There was a significant increase in motor recovery as well as body weight from postoperative day (POD) 7 under constant darkness. However, spontaneous elevation of endogenous melatonin in cerebrospinal fluid was seen at POD 3 in all of the SCI rats, which was enhanced in SCI + DD group. Augmented melatonin concentration under constant dark condition resulted in facilitation of neuronal differentiation as well as inhibition of primary cell death. In the rostrocaudal region, elevated endogenous melatonin concentration promoted neural remodeling in acute phase including oligodendrogenesis, excitatory synaptic formation, and axonal outgrowth. The changes were mediated via NAS-TrkB-AKT/ERK signal transduction co-regulated by the circadian clock mechanism, leading to rapid motor recovery. In contrast, exposure to constant light exacerbated the inflammatory responses and neuroglial loss. These results suggest that light/dark control in the acute phase might be a considerable environmental factor for a favorable prognosis after SCI.
我们研究了实验性脊髓损伤(SCI)后,环境光照条件调节内源性褪黑素分泌对神经修复的影响。将大鼠随机分为三组:SCI + L/D(12/12小时光照/黑暗)组、SCI + LL(24小时持续光照)组和SCI + DD(24小时持续黑暗)组。在诱导脊髓损伤前2周预先施加受控的光照/黑暗周期。在术后第7天起,持续黑暗条件下运动功能恢复以及体重均有显著增加。然而,所有SCI大鼠在术后第3天脑脊液中内源性褪黑素均自发升高,在SCI + DD组中升高更为明显。持续黑暗条件下褪黑素浓度升高促进了神经元分化并抑制了原代细胞死亡。在头尾区域,内源性褪黑素浓度升高促进了急性期的神经重塑,包括少突胶质细胞生成、兴奋性突触形成和轴突生长。这些变化是通过由生物钟机制共同调节的NAS-TrkB-AKT/ERK信号转导介导的,从而导致运动功能快速恢复。相反,持续光照会加剧炎症反应和神经胶质细胞损失。这些结果表明,急性期的光照/黑暗控制可能是SCI后预后良好的一个重要环境因素。