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重症肌无力大鼠的重复神经刺激与抽搐张力对比

Repetitive nerve stimulation vs. twitch tension in rats with EAMG.

作者信息

Thompson P A, Barohn R A, Krolick K A

机构信息

Department of Microbiology, University of Texas Health Science Center, San Antonio 78284.

出版信息

Muscle Nerve. 1992 Jan;15(1):94-100. doi: 10.1002/mus.880150116.

DOI:10.1002/mus.880150116
PMID:1732768
Abstract

Two methods were compared with regard to their ability to detect acetylcholine receptor-dependent neuromuscular dysfunction in rats with experimental autoimmune myasthenia gravis. In both cases, detection of AChR impairment required amplification of symptoms by administration of the AChR antagonist curare and appeared to be directly related to increasing levels of circulating anti-AChR antibodies. First, in vivo evaluations of decremental compound motor action potentials following repetitive nerve stimulation were performed by electromyography. Impaired neuromuscular function (i.e., greater than 10% decrement) was noted only after rats had been immunized twice with AChR, requiring levels of circulating anti-AChR antibody greater than about 200 micrograms/mL in serum. In contrast, the direct in vitro evaluation of stimulated isometric twitch tension appeared to be more sensitive in that impaired AChR-dependent muscle contraction was clearly observed following a single AChR immunization, and, as shown previously, required anti-AChR antibody levels of about 50 micrograms/mL in serum. Further discussion is presented concerning the advantages and disadvantages associated with each method of monitoring disease.

摘要

比较了两种方法检测实验性自身免疫性重症肌无力大鼠中乙酰胆碱受体依赖性神经肌肉功能障碍的能力。在这两种情况下,检测乙酰胆碱受体损伤都需要通过给予乙酰胆碱受体拮抗剂箭毒来放大症状,并且似乎与循环抗乙酰胆碱受体抗体水平的升高直接相关。首先,通过肌电图对重复神经刺激后复合运动动作电位的递减进行体内评估。仅在大鼠用乙酰胆碱受体免疫两次后才观察到神经肌肉功能受损(即递减大于10%),这需要血清中循环抗乙酰胆碱受体抗体水平大于约200微克/毫升。相比之下,对刺激的等长抽搐张力的直接体外评估似乎更敏感,因为在单次乙酰胆碱受体免疫后就清楚地观察到了乙酰胆碱受体依赖性肌肉收缩受损,并且如先前所示,血清中抗乙酰胆碱受体抗体水平需要约50微克/毫升。文中进一步讨论了与每种疾病监测方法相关的优缺点。

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1
Repetitive nerve stimulation vs. twitch tension in rats with EAMG.重症肌无力大鼠的重复神经刺激与抽搐张力对比
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Single-fiber electromyography in experimental autoimmune myasthenia gravis.实验性自身免疫性重症肌无力的单纤维肌电图
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Resistance to experimental autoimmune myasthenia gravis in genetically inbred rats. Association with decreased amounts of in situ acetylcholine receptor-antibody complexes.基因近交系大鼠对实验性自身免疫性重症肌无力的抗性。与原位乙酰胆碱受体 - 抗体复合物数量减少有关。
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[Clinical correlation of anti-receptor antibody titer, sensitivity to curare and electromyographic changes in experimental autoimmune myasthenia gravis].[实验性自身免疫性重症肌无力中抗受体抗体滴度、对箭毒的敏感性与肌电图变化的临床相关性]
Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1990 Oct;23(5):293-6, 320.
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[Acetylcholine receptor antibody titer, sensitivity to curare electromyogram and disease severity in myasthenia gravis].[重症肌无力中乙酰胆碱受体抗体滴度、对箭毒的肌电图敏感性及疾病严重程度]
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Lewis rats given antibodies against denatured acetylcholine receptor become resistant to induction of experimental autoimmune myasthenia gravis.
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Standardization of the experimental autoimmune myasthenia gravis (EAMG) model by immunization of rats with Torpedo californica acetylcholine receptors--Recommendations for methods and experimental designs.通过用加州电鳐乙酰胆碱受体免疫大鼠对实验性自身免疫性重症肌无力(EAMG)模型进行标准化——方法和实验设计建议
Exp Neurol. 2015 Aug;270:18-28. doi: 10.1016/j.expneurol.2015.03.010. Epub 2015 Mar 18.