Thornell L E, Sjöström M, Mattsson C H, Heilbronn E
J Neurol Sci. 1976 Oct;29(2-4):389-410. doi: 10.1016/0022-510x(76)90187-8.
The morphology of motor end-plates in rabbits immunized with Torpedo nicotinic acetylcholine receptor (nAChR) has been studied by light and electron microscopy. Rabbits were studied either after one period of paralysis, some in parallel with electrophysiological recordings of MEPPs and EPPs and of Naja naja alpha-neurotoxin binding properties or after recovery followed by a second paralysis. Changes in the sub-neural apparatus were noted after cholinesterase staining only in the latter group. Ultrastructurally, however, most end-plates in both groups contained a wide range of abnormalities. Many were similar in appearance to those observed in human myasthenia gravis (MG). This further supports the theory that immunized rabbits can be used as a model for myasthenia gravis. In the rabbits with 1 period of paralysis an acute stage of influence on the neuromuscular junction seemed to be present while simplified motor end-plates typical for human MG were mostly found in rabbits with 2 periods of paralysis. Short post-synaptic folds in conjugation with thickeneed membrane-bound vesicles at their tops, inside the basement membrane, were frequently observed. These were interpreted as if the crests of the folds containing nAChR had degenerated and had been budded off. If so, a large number of receptor sites had been lost which would be one possible explanation for the lowered capacity of the muscles to bind Naja naja alpha-neurotoxin. Membrane thickenings with projections and striations were interpreted as reflecting ACh receptors and were observed in the post-junctional membrane without proximity to the nerve terminal. The degeneration of the top of the post-synaptic folds and the occurrence of receptors at other locations within the motor end-plate will result in a widened distance between the nerve terminal and the receptors, which can explain previous interpretations of a presynaptic defect in MG.
利用光镜和电镜研究了用鱼雷烟碱型乙酰胆碱受体(nAChR)免疫的家兔运动终板的形态。对家兔进行了研究,一组是在一次麻痹期后,部分家兔同时进行了微小终板电位(MEPPs)、终板电位(EPPs)以及眼镜蛇α-神经毒素结合特性的电生理记录;另一组是在恢复后再进行第二次麻痹。仅在后一组中,经胆碱酯酶染色后观察到神经下装置的变化。然而,从超微结构来看,两组中的大多数终板都存在广泛的异常。许多终板的外观与在人类重症肌无力(MG)中观察到的相似。这进一步支持了免疫家兔可作为重症肌无力模型的理论。在经历一次麻痹期的家兔中,似乎存在对神经肌肉接头影响的急性期,而在经历两次麻痹期的家兔中,大多发现了人类MG典型的简化运动终板。在基底膜内,经常观察到突触后褶皱短且其顶部伴有增厚的膜结合囊泡。这些被解释为好像含有nAChR的褶皱嵴已经退化并脱落。如果是这样,大量的受体位点就会丢失,这可能是肌肉结合眼镜蛇α-神经毒素能力降低的一个原因。在没有靠近神经末梢的突触后膜中观察到有突起和条纹的膜增厚,被解释为反映了乙酰胆碱受体。突触后褶皱顶部的退化以及运动终板内其他位置出现受体,将导致神经末梢与受体之间的距离增宽,这可以解释之前对MG中突触前缺陷的解释。