Ping Xingjie, Jiang Kewen, Lee Seung-Young, Cheng Ji-Xing, Jin Xiaoming
1 Department of Anatomy and Cell Biology, Stark Neuroscience Research Institute, Indiana Spinal Cord and Brain Injury Research Group, Indiana University School of Medicine , Indianapolis, Indiana.
J Neurotrauma. 2014 Jul 1;31(13):1172-9. doi: 10.1089/neu.2013.3147. Epub 2014 May 13.
The initial pathological changes of diffuse axonal injury following traumatic brain injury (TBI) include membrane disruption and loss of ionic homeostasis, which further lead to dysfunction of axonal conduction and axon disconnection. Resealing the axolemma is therefore a potential therapeutic strategy for the early treatment of TBI. Monomethoxy poly (ethylene glycol)-poly (D, L-lactic acid) di-block copolymer micelles (mPEG-PDLLA) have been shown to restore depressed compound action potentials (CAPs) of spinal axons and promote functional recovery after spinal cord injury. Here, we evaluate the effect of the micelles on repairing the injured cortical axons following TBI. Adult mice subjected to controlled cortical impact (CCI) were treated with intravenous injection of the micelles at 0 h or 4 h after injury. Evoked CAPs were recorded from the corpus callosum of coronal cortical slices at 2 days after injury. The CCI caused significant decreases in the amplitudes of two CAP peaks that were respectively generated by the faster myelinated axons and slower unmyelinated axons. Micelle treatment at both 0 h and 4 h after CCI resulted in significant increases in both CAP peak amplitudes. Injection of fluorescent dye-labeled micelles revealed high fluorescent staining in cortical gray and white matters underneath the impact site. Labeling membrane-perforated neurons by injecting a membrane impermeable dye Texas Red-labeled dextran into lateral ventricles at 2 h post-CCI revealed that immediate micelle injection after CCI did not reduce the number of dye-stained cortical neurons and dentate granule cells of the hippocampus, indicating its ineffectiveness in repairing plasma membrane of neuronal somata. We conclude that intravenous administration of mPEG-PDLLA micelles immediately or at 4 h after TBI allows brain penetration via the compromised blood brain-barrier, and thereby improves the function of both myelinated and unmyelinated axons of the corpus callosum.
创伤性脑损伤(TBI)后弥漫性轴索损伤的初始病理变化包括细胞膜破坏和离子稳态丧失,这进一步导致轴索传导功能障碍和轴突离断。因此,重新封闭轴膜是TBI早期治疗的一种潜在治疗策略。单甲氧基聚(乙二醇)-聚(D,L-乳酸)二嵌段共聚物胶束(mPEG-PDLLA)已被证明可恢复脊髓轴突降低的复合动作电位(CAPs),并促进脊髓损伤后的功能恢复。在此,我们评估了该胶束对TBI后受损皮质轴突修复的影响。成年小鼠接受控制性皮质撞击(CCI),在损伤后0小时或4小时静脉注射该胶束进行治疗。在损伤后2天,从冠状皮质切片的胼胝体记录诱发的CAPs。CCI导致分别由较快的有髓轴突和较慢的无髓轴突产生的两个CAP峰的振幅显著降低。CCI后0小时和4小时进行胶束治疗均导致两个CAP峰振幅显著增加。注射荧光染料标记的胶束后,在撞击部位下方的皮质灰质和白质中显示出高荧光染色。在CCI后2小时通过向侧脑室注射膜不可渗透的染料德克萨斯红标记的葡聚糖来标记膜穿孔神经元,结果显示CCI后立即注射胶束并未减少海马体中染料染色的皮质神经元和齿状颗粒细胞的数量,表明其在修复神经元胞体的质膜方面无效。我们得出结论,在TBI后立即或4小时静脉注射mPEG-PDLLA胶束可通过受损的血脑屏障进入大脑,从而改善胼胝体中有髓和无髓轴突的功能。