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Physiological Roles of Neurite Outgrowth Inhibitors in Myelinated Axons of the Central Nervous System – Implications for the Therapeutic Neutralization of Neurite Outgrowth Inhibitors

机译:神经突生长抑制剂在中枢神经系统髓鞘轴突中的生理作用–对神经突生长抑制剂的治疗中和意义

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摘要

It has long been recognized that the central nervous system (CNS) exhibits only limited capacity for axonal regeneration following injury. It has been proposed that myelin-associated inhibitory molecules are responsible for the nonpermissive nature of the CNS environment to axonal regeneration. Experimental strategies to enhance regeneration by neutralizing these inhibitory molecules are rapidly advancing toward clinical application. It is therefore important that the physiological distribution and functions of these supposed inhibitory molecules should be understood. In this review, we examine the distribution of these inhibitors of neurite outgrowth in relation to the longitudinal polarization of the myelinated axon into the node of Ranvier and associated domains and explore their potential domain specific physiological functions. Potential implications for the therapeutic strategy of neutralizing these inhibitory molecules to promote neural repair are discussed.
机译:早就认识到中枢神经系统(CNS)损伤后轴突再生能力有限。已经提出,髓磷脂相关的抑制分子负责CNS环境对轴突再生的非容许性质。通过中和这些抑制性分子来增强再生的实验策略正迅速向临床应用发展。因此,重要的是应了解这些假定的抑制分子的生理分布和功能。在这篇综述中,我们检查了神经突生长抑制剂的分布与髓鞘轴突进入Ranvier和相关区域的结节的纵向极化有关,并探讨了它们潜在的区域特定生理功能。讨论了中和这些抑制性分子以促进神经修复的治疗策略的潜在含义。

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