Cambridge Centre for Brain Repair, University of Cambridge, UK.
Horm Behav. 2010 Jan;57(1):56-62. doi: 10.1016/j.yhbeh.2009.06.004. Epub 2009 Jun 16.
Remyelination following central nervous system (CNS) demyelination restores rapid saltatory conduction of action potentials and contributes to the maintenance of axonal integrity. This robust regenerative phenomenon stands in contrast to the limited repair capacity that is characteristic of CNS neuronal injury. However, despite its efficiency in experimental models and some clinical diseases, remyelination failure becomes an increasingly pronounced feature of the pathology of chronic multiple sclerosis (MS) lesions. Chronic demyelination predisposes axons to atrophy, an irreversible event that is a major pathological correlate of progressive functional decline. This has created a compelling case for developing therapies that promote remyelination: evidence from experimental animal models suggests that hormones may have a beneficial role to play in this regard.
中枢神经系统(CNS)脱髓鞘后发生的髓鞘再生可恢复动作电位的快速跳跃传导,并有助于维持轴突的完整性。这种强大的再生现象与 CNS 神经元损伤的有限修复能力形成鲜明对比。然而,尽管在实验模型和某些临床疾病中效率很高,但髓鞘再生失败成为慢性多发性硬化(MS)病变病理学的一个日益显著的特征。慢性脱髓鞘使轴突容易萎缩,而轴突萎缩是进行性功能下降的主要病理相关因素,这一现象使开发促进髓鞘再生的疗法具有很强的说服力:来自实验动物模型的证据表明,激素在这方面可能具有有益的作用。