Literature DB >> 28153715

Neuromuscular excitability changes produced by sustained voluntary contraction and response to mexiletine in myotonia congenita.

Federica Ginanneschi1, Andrea Mignarri2, Sabrina Lucchiari3, Gianna Ulzi3, Giacomo P Comi3, Alessandro Rossi2, Maria Teresa Dotti2.   

Abstract

OBJECTIVE: To investigate the cause of transient weakness in myotonia congenita (MC) and the mechanism of action of mexiletine in reducing weakness.
METHODS: The changes in neuromuscular excitability produced by 1min of maximal voluntary contractions (MVC) were measured on the amplitude of compound muscle action potentials (CMAP) in two patients with either recessive or dominant MC, compared to control values obtained in 20 healthy subjects. Measurements were performed again in MC patients after mexiletine therapy.
RESULTS: Transient reduction in maximal CMAP amplitude lasting several minutes after MVC was evident in MC patients, whereas no change was observed in controls. Mexiletine efficiently reduced this transient CMAP depression in both patients. DISCUSSION: Transient CMAP depression following sustained MVC may represent the electrophysiological correlate of the weakness clinically experienced by the patients. In MC, the low chloride conductance could induce self-sustaining action potentials after MVC, determining progressive membrane depolarization and a loss of excitability of muscle fibers, thus resulting in transient paresis. Mexiletine may prevent conduction block due to excessive membrane depolarization, thus reducing the transient CMAP depression following sustained MVC.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Activité naturelle; Canal sodique; Chloride conductance; Conductance chlore; Faiblesse; Myotonia; Myotonie; Natural activity; Sodium channel; Weakness

Mesh:

Substances:

Year:  2017        PMID: 28153715     DOI: 10.1016/j.neucli.2017.01.003

Source DB:  PubMed          Journal:  Neurophysiol Clin        ISSN: 0987-7053            Impact factor:   3.734


  4 in total

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3.  Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation.

Authors:  Chenyu Zhao; DongFang Tang; Hui Huang; Haiyan Tang; Yuan Yang; Min Yang; Yingying Luo; Huai Tao; Jianguang Tang; Xi Zhou; Xiaoliu Shi
Journal:  PLoS One       Date:  2020-05-14       Impact factor: 3.240

4.  Improving the understanding of how patients with non-dystrophic myotonia are selected for myotonia treatment with mexiletine (NaMuscla): outcomes of treatment impact using a European Delphi panel.

Authors:  Ann-Marie Chapman; Marieke Schurer; Laure Weijers; Amer Omar; Hiba Lee; Alla Zozulya Weidenfeller; Crispin Ellis; Shaneil Sonecha; Christiane Schneider-Gold
Journal:  BMC Neurol       Date:  2021-12-01       Impact factor: 2.474

  4 in total

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