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成年大鼠小脑浦肯野细胞暴露于海藻酸会模拟轴突切断的效应。

Exposure to kainic acid mimics the effects of axotomy in cerebellar Purkinje cells of the adult rat.

作者信息

Rossi F, Borsello T, Strata P

机构信息

Department of Human Anatomy and Physiology, University of Turin, Italy.

出版信息

Eur J Neurosci. 1994 Mar 1;6(3):392-402. doi: 10.1111/j.1460-9568.1994.tb00282.x.

Abstract

We have investigated the long-term structural changes which affect Purkinje cells exposed to a single dose of kainic acid. Following intraparenchymal injection of the excitotoxin in the cerebellar cortex (1 microliter of a 1 mg/ml solution), Purkinje cells which survived within the lesioned area or close to its edges showed remarkable axonal abnormalities, involving the formation of torpedoes, hypertrophy of recurrent collaterals and atrophy of the corticofugal portion of the axon. In addition, their dendritic trees were often affected by conspicuous regressive alterations. The climbing fibres contacting these Purkinje cells were characterized by thick perisomatic plexuses, whereas their peridendritic branches were atrophic. The dendrites innervated by such atrophic olivary arbours were studded with huge numbers of newly formed spines. These alterations were already present a few days after kainic acid administration and persisted for the total period of observation of 6 months after the lesion. The remarkable similarity between the abnormalities of Purkinje cells exposed to kainic acid and those observed after axotomy indicates that in these two conditions common mechanisms determine analogous long-lasting modifications in the affected neurons. It is proposed that kainic acid-induced intracellular calcium overload disrupts cytoskeletal components and impairs axonal transport, thus depriving the affected Purkinje cells of retrograde trophic influences from their target neurons. As a consequence the affected neurons undergo long-lasting regressive modifications and compensatory remodelling phenomena.

摘要

我们研究了影响单次注射 kainic 酸后浦肯野细胞的长期结构变化。在小脑皮质实质内注射兴奋性毒素(1 微升 1 毫克/毫升溶液)后,在损伤区域内或其边缘存活的浦肯野细胞显示出明显的轴突异常,包括鱼雷样结构的形成、回返侧支的肥大以及轴突皮质传出部分的萎缩。此外,它们的树突通常受到明显的退行性改变的影响。与这些浦肯野细胞接触的攀缘纤维的特点是胞体周围有浓密的神经丛,而其树突周围分支萎缩。由这种萎缩的橄榄神经分支支配的树突上布满了大量新形成的棘突。这些改变在注射 kainic 酸后几天就已出现,并在损伤后长达 6 个月的观察期内持续存在。暴露于 kainic 酸的浦肯野细胞异常与轴突切断后观察到的异常之间的显著相似性表明,在这两种情况下,共同的机制决定了受影响神经元中类似的长期改变。有人提出,kainic 酸诱导的细胞内钙超载会破坏细胞骨架成分并损害轴突运输,从而使受影响的浦肯野细胞失去来自其靶神经元的逆行营养影响。因此,受影响的神经元会经历长期的退行性改变和代偿性重塑现象。

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