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新生儿实验性自身免疫性重症肌无力

Neonatal experimental autoimmune myasthenia gravis.

作者信息

Sanders D B, Cobb E E, Winfield J B

出版信息

Muscle Nerve. 1978 Mar-Apr;1(2):146-50. doi: 10.1002/mus.880010207.

Abstract

Neonatal rats born of and nursed by mothers immunized with Torpedo acetylcholine receptor protein developed a defect of neuromuscular transmission as indicated by reduced miniature endplate potential amplitudes. It is likely that antibodies to the Torpedo receptor protein were passively transferred to the neonates in the milk. With the exception of the route of transfer, this neonatal form of experimental autoimmune myasthenia gravis appears to be similar to its human counterpart, and thus can serve as an experimental model.

摘要

用乙酰胆碱受体蛋白免疫的母鼠所生并由其哺育的新生大鼠,出现了神经肌肉传递缺陷,表现为微小终板电位振幅降低。很可能抗乙酰胆碱受体蛋白的抗体通过乳汁被动转移给了新生大鼠。除了转移途径外,这种新生儿型实验性自身免疫性重症肌无力似乎与其人类对应疾病相似,因此可作为一种实验模型。

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