Thomas P K
Muscle Nerve. 1982;5(9S):S117-21.
The primary sensory neurons are unique in possessing one axon that lies within the peripheral nervous system and another that extends into the central nervous system. The two, therefore, have different environments and are associated with different supporting cells. Most of the distal ("dying-back") axonopathies that have so far been studied display simultaneous distal degeneration of both the peripherally and centrally directed axons of the dorsal root ganglion cells ("central-peripheral distal axonopathy"); others may display selective distal degeneration of the peripheral axons. Recent electrophysiological (sensory nerve conduction and somatosensory evoked potentials) and neuropathological studies have demonstrated that a further pattern in distal axonopathies is a selective or predominant degeneration of the centrally directed axons. This has been suggested for hereditary spastic paraplegia and clioquinol neurotoxicity. Persistent symptoms in central and central-peripheral distal axonopathies may result from imperfect regeneration of the centrally directed axons.
初级感觉神经元的独特之处在于,它有一条位于外周神经系统的轴突,还有一条延伸至中枢神经系统的轴突。因此,这两条轴突所处环境不同,且与不同的支持细胞相关联。迄今为止所研究的大多数远端(“逆行性”)轴索性神经病都表现为背根神经节细胞的外周和中枢定向轴突同时发生远端变性(“中枢 - 外周远端轴索性神经病”);其他一些情况可能表现为外周轴突的选择性远端变性。最近的电生理研究(感觉神经传导和体感诱发电位)及神经病理学研究表明,远端轴索性神经病的另一种模式是中枢定向轴突的选择性或主要变性。遗传性痉挛性截瘫和氯碘喹啉神经毒性就被认为属于这种情况。中枢性和中枢 - 外周远端轴索性神经病的持续症状可能是由于中枢定向轴突的再生不完善所致。