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犬遗传性共济失调:超微结构观察

Canine inherited ataxia: ultrastructural observations.

作者信息

Troncoso J C, Cork L C, Price D L

出版信息

J Neuropathol Exp Neurol. 1985 Mar;44(2):165-75. doi: 10.1097/00005072-198503000-00005.

Abstract

Canine Inherited Ataxia is inherited as an autosomal recessive trait in Gordon Setters. This animal model shares features with certain human cerebellar degenerations and offers the opportunity to examine brain tissue at various stages during the evolution of disease. The present investigation focuses on the morphometric and ultrastructural changes of cerebellar neurons. Purkinje and granule cells are the principal intrinsic neurons at risk. The size of Purkinje cells decreases, axonal degeneration is an important feature of the pathology, and synaptic abnormalities occur in the cerebellar glomeruli and deep nuclei of the cerebellum. The sequence and nature of synaptic changes in the molecular layer suggest that the degenerative process begins in Purkinje cells and that granule cells may be secondarily affected.

摘要

犬遗传性共济失调在戈登雪达犬中作为常染色体隐性性状遗传。这种动物模型与某些人类小脑变性具有共同特征,并为在疾病发展的不同阶段检查脑组织提供了机会。本研究聚焦于小脑神经元的形态计量学和超微结构变化。浦肯野细胞和颗粒细胞是主要的易损固有神经元。浦肯野细胞的大小减小,轴突变性是病理学的一个重要特征,并且在小脑小球和小脑深部核团中出现突触异常。分子层中突触变化的顺序和性质表明,退行性过程始于浦肯野细胞,颗粒细胞可能继发受到影响。

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