神经肌肉连接处紊乱

D. Hilton‐Jones, Jacqueline A Palace
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引用次数: 0

摘要

本章着眼于两种根本不同的病理过程如何与神经肌肉连接处的疾病相关:获得性疾病,其中自身抗体直接针对神经或肌肉受体或离子通道;罕见的遗传性疾病,缺陷可能发生在突触前或突触后。获得性神经肌肉连接障碍与针对其中一个离子通道的抗体有关。已知有三种自身免疫性疾病影响如此小的区域,这一事实可能是由于神经肌肉连接处不像周围神经,不包含在血液-神经屏障中,它在神经末梢附近停止,因此可能暴露于循环的体液攻击中。遗传性疾病可能影响突触前过程(乙酰胆碱再合成、包装或释放)、乙酰胆碱酯酶结合或突触后功能(乙酰胆碱受体数量或定位)。在讨论个体疾病时,发病机制要更详细地考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disorders of the neuromuscular junction
This chapter looks at how two fundamentally different pathological processes are associated with disease at the neuromuscular junction: acquired disorders in which autoantibodies are directed against nerve or muscle receptor or ion channels; rare inherited conditions in which the defect may be pre- or postsynaptic. The acquired neuromuscular junction disorders are associated with antibodies directed against one of the ion channels. The fact that there are three autoimmune disorders known to affect such a small region may be explained by the neuromuscular junction, unlike the peripheral nerve, not being contained within the blood–nerve barrier, which stops just short of the nerve terminal, and thus being potentially exposed to circulating humoral attack. The inherited disorders may affect presynaptic processes (acetylcholine resynthesis, packaging, or release), acetylcholinesterase binding, or postsynaptic function (acetylcholine receptor numbers or localization). Pathogenic mechanisms are considered in more detail when discussing individual disorders.
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