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来自一名米勒-费希尔综合征患者的免疫球蛋白G能迅速且可逆地抑制小鼠神经肌肉接头处的诱发量子释放。

Immunoglobulin G from a patient with Miller-Fisher syndrome rapidly and reversibly depresses evoked quantal release at the neuromuscular junction of mice.

作者信息

Buchwald B, Weishaupt A, Toyka K V, Dudel J

机构信息

Physiologisches Institut der Technische Universität München Biedersteiner, Germany.

出版信息

Neurosci Lett. 1995 Dec 8;201(2):163-6. doi: 10.1016/0304-3940(95)12155-2.

Abstract

A neuromuscular blocking factor has been described in the serum of patients with Miller-Fisher syndrome (MFS). We here examined the effect of immunoglobulins (Ig) on neuromuscular transmission in mice recording quantal endplate currents by means of a perfused macro-patch-clamp electrode. Ig and IgM- and IgG-fractions from an anti-GQ1b-positive patient with typical MFS were highly purified. After application of MFS-IgG, quantal release decreased 1000-fold within 2 min. Returning to control solution the average release came back to the baseline level within 4 min. In contrast, control-IgG and MFS-IgM did not cause any blocking effect. The very fast and fully reversible presynaptic blockade of release caused by the highly purified IgG-fraction may be one factor producing muscle weakness in MFS.

摘要

在米勒-费雪综合征(MFS)患者的血清中已发现一种神经肌肉阻断因子。我们在此通过灌注式巨膜片钳电极记录量子化终板电流,研究了免疫球蛋白(Ig)对小鼠神经肌肉传递的影响。从一名典型MFS的抗GQ1b阳性患者中高度纯化了Ig以及IgM和IgG组分。应用MFS-IgG后,量子化释放量在2分钟内下降了1000倍。回到对照溶液后,平均释放量在4分钟内恢复到基线水平。相比之下,对照IgG和MFS-IgM未产生任何阻断作用。高度纯化的IgG组分引起的释放的非常快速且完全可逆的突触前阻断可能是导致MFS患者肌肉无力的一个因素。

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