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进行性轴索性神经病:拳师犬的一种遗传性神经病变。3. 外周轴突病变,特别提及神经根。

Progressive axonopathy: an inherited neuropathy of boxer dogs. 3. The peripheral axon lesion with special reference to the nerve roots.

作者信息

Griffiths I R, McCulloch M C, Abrahams S

出版信息

J Neurocytol. 1986 Feb;15(1):109-20. doi: 10.1007/BF02057909.

Abstract

Progressive axonopathy is an autosomal recessive inherited neuropathy of Boxer dogs with lesions in the CNS and PNS. This paper describes the axonal changes in the lumbar and cervical nerve roots and tibial nerve. By 2 months of age the proximal paranodal areas of many larger diameter fibres show small axonal swellings, sometimes with attenuation or loss of the associated myelin sheath. Axoplasmic changes within swollen and non-swollen fibres include disorganization of the peripheral neurofilaments and small accumulations of vesicles and vesiculo-tubular profiles, particularly in the sub-axolemmal area. Occasional fibres, more often in the cervical roots, are massively distended with disorganized neurofilaments. The frequency of the membranous accumulations decreases with progression of the disease. Many axons show a markedly irregular or corrugated outline and are surrounded by an attenuated sheath. The peripheral axonal cytoskeleton is disorganized and misaligned, whereas the central structures maintain a more normal arrangement. Regenerating axonal clusters are common in the cervical ventral roots but occur infrequently in the lumbar roots. Similar axonal changes occur in the peripheral nerves but at a much lower frequency. Any membranous accumulations or cytoskeletal disorganization are more probable in the proximal tibial nerves, while the frequency of axonal degeneration and regeneration increases distally. The morphological appearances indicate gross disturbances in axon-sheath cell relationships and suggest that abnormalities in the transport of various axoplasmic organelles may be involved in the pathogenesis of the axonal lesion.

摘要

进行性轴索性神经病是拳师犬的一种常染色体隐性遗传性神经病,中枢神经系统和周围神经系统均有病变。本文描述了腰神经根、颈神经根和胫神经的轴突变化。在2月龄时,许多直径较大的纤维的近端结旁区出现小的轴突肿胀,有时伴有相关髓鞘的变薄或缺失。肿胀和未肿胀纤维内的轴浆变化包括外周神经丝的紊乱以及小泡和小泡-管状结构的少量聚集,特别是在轴膜下区域。偶尔有纤维,更常见于颈神经根,被紊乱的神经丝大量扩张。随着疾病进展,膜性聚集物的频率降低。许多轴突显示出明显不规则或波纹状的轮廓,并被变薄的髓鞘包围。外周轴突细胞骨架紊乱且排列错位,而中央结构保持更正常的排列。再生轴突簇在颈前根很常见,但在腰神经根中很少出现。外周神经也会出现类似的轴突变化,但频率要低得多。在胫神经近端,任何膜性聚集或细胞骨架紊乱的可能性更大,而轴突变性和再生的频率在远端增加。形态学表现表明轴突-髓鞘细胞关系存在严重紊乱,并提示各种轴浆细胞器运输异常可能参与了轴突病变的发病机制。

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