Combination treatment with anti-Nogo-A and chondroitinase ABC is more effective than single treatments at enhancing functional recovery after spinal cord injury

被引:89
|
作者
Zhao, Rong-Rong [1 ]
Andrews, Melissa R. [1 ]
Wang, Difei [1 ]
Warren, Philippa [1 ]
Gullo, Miriam [2 ]
Schnell, Lisa [2 ]
Schwab, Martin E. [2 ,3 ]
Fawcett, James W. [1 ]
机构
[1] Univ Cambridge, Dept Clin Neurosci, Cambridge Ctr Brain Repair, Cambridge, England
[2] Univ Zurich, Brain Res Inst, CH-8006 Zurich, Switzerland
[3] Fed Inst Technol ETH Zurich, Dept Hlth Sci & Technol, Zurich, Switzerland
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
axon regeneration; chondroitinase; Nogo-A; plasticity; rehabilitation; spinal cord; SULFATE PROTEOGLYCAN; EXTRACELLULAR-MATRIX; NEURITE OUTGROWTH; PROMOTES RECOVERY; FORELIMB FUNCTION; STAIRCASE TEST; REGENERATION; RATS; PLASTICITY; GROWTH;
D O I
10.1111/ejn.12276
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Anti-Nogo-A antibody and chondroitinase ABC (ChABC) enzyme are two promising treatments that promote functional recovery after spinal cord injury (SCI). Treatment with them has encouraged axon regeneration, sprouting and functional recovery in a variety of spinal cord and central nervous system injury models. The two compounds work, in part, through different mechanisms, so it is possible that their effects will be additive. In this study, we used a rat cervical partial SCI model to explore the effectiveness of a combination of anti-Nogo-A, ChABC, and rehabilitation. We found that spontaneous recovery of forelimb functions reflects the extent of the lesion on the ipsilateral side. We applied a combination treatment with acutely applied anti-Nogo-A antibody followed by delayed ChABC treatment starting at 3weeks after injury, and rehabilitation starting at 4weeks, to accommodate the requirement that anti-Nogo-A be applied acutely, and that rehabilitation be given after the cessation of anti-Nogo-A treatment. We found that single treatment with either anti-Nogo-A or ChABC, combined with rehabilitation, produced functional recovery of similar magnitude. The combination treatment, however, was more effective. Both single treatments produced increases in sprouting and axon regeneration, but the combination treatment produced greater increases. Anti-Nogo-A stimulated growth of a greater number of axons with a diameter of >3m, whereas ChABC treatment stimulated increased growth of finer axons with varicosities. These results point to different functions of Nogo-A and chondroitin sulfate proteoglycans in axonal regeneration. The combination of anti-Nogo-A, ChABC and rehabilitation shows promise for enhancing functional recovery after SCI.
引用
收藏
页码:2946 / 2961
页数:16
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