Cummings J F, de Lahunta A, Summers B A, Mohammed H O, Divers T J, Valentine B A, Trembicki-Graves K
College of Veterinary Medicine, Cornell University, Ithaca, NY 14853-6401.
Acta Neuropathol. 1993;85(3):291-7. doi: 10.1007/BF00227725.
Equine motor neuron disease (EMND) is a sporadic, progressive neurodegenerative disorder that has been identified recently in horses of different breeds in North America. The cause is unknown. Pathologic changes which occur in spinal and certain brain stem motor neurons include chromatolysis, swelling, neurofilamentous accumulation, and development of eosinophilic cytoplasmic inclusions. Punctate eosinophilic inclusions, the type usually encountered in degenerating neurons, resembled Bunina bodies at the light microscopic level, but differed in their ultrastructural composition. These and less common but larger juxtanuclear inclusions appeared to be aggregated vesicular residues of membranous organelle degradation. The third kind of eosinophilic inclusion was a marginated derivative of endoplasmic reticulum and consisted of large membrane-bound accumulations of finely granular material. It was concluded that, although the distribution and nature of the lesions in EMND appeared similar to those of human motor neuron disease, none of the equine eosinophilic inclusions duplicated the ultrastructure of Bunina bodies.
马运动神经元病(EMND)是一种散发性、进行性神经退行性疾病,最近在北美的不同品种马匹中被发现。病因不明。脊髓和某些脑干运动神经元发生的病理变化包括染色质溶解、肿胀、神经丝积聚以及嗜酸性细胞质内含物的形成。点状嗜酸性内含物是在退化神经元中通常遇到的类型,在光学显微镜下类似于布尼纳小体,但超微结构组成不同。这些以及不太常见但更大的核旁内含物似乎是膜性细胞器降解的聚集性囊泡残余物。第三种嗜酸性内含物是内质网的边缘衍生物,由大量细颗粒物质的膜结合积聚物组成。得出的结论是,尽管EMND中的病变分布和性质似乎与人类运动神经元病相似,但马的嗜酸性内含物均未复制布尼纳小体的超微结构。