Literature DB >> 6270549

Membrane defects in paramyotonia congenita with and without myotonia in a warm environment.

F Lehmann-Horn, R Rüdel, R Dengler, H Lorković, A Haass, K Ricker.   

Abstract

Three patients with paramyotonia congenita and 3 control persons were biopsied for an in vitro investigation of the sarcolemmal membrane parameters and of the contractile properties of paramyotonic muscle. At 37 degrees C, paramyotonic muscle fibers had normal resting potentials, but on cooling to 27 degrees C they depolarized. Depolarization to -60 mV caused spontaneous activity, and further depolarization to -40 mV caused inexcitability. Depolarization could be prevented by the application of tetrodotoxin, a finding suggesting a defect in the Na channels. Analysis of the membrane current densities using voltage clamps with 3 microelectrodes revealed that in paramyotonic patients at 37 degrees C all component conductances were normal, except for a decreased Cl conductance in the patient who had myotonia in a warm environment. At 27 degrees C, the Na and Cl conductances were abnormally high. The K conductance was always normal. The results explain the clinical symptoms of weakness and paralysis. Potassium- and caffeine-contracture experiments gave normal results. The clinical symptom of paramyotonic stiffness, therefore, has not been explained by these studies.

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Year:  1981        PMID: 6270549     DOI: 10.1002/mus.880040508

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  19 in total

1.  Neuromyotonia in hereditary motor neuropathy.

Authors:  A F Hahn; A W Parkes; C F Bolton; S A Stewart
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-03       Impact factor: 10.154

Review 2.  Voltage-sensor mutations in channelopathies of skeletal muscle.

Authors:  Stephen C Cannon
Journal:  J Physiol       Date:  2010-02-15       Impact factor: 5.182

3.  Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

Authors:  M C Koch; K Ricker; M Otto; T Grimm; K Bender; B Zoll; P S Harper; F Lehmann-Horn; R Rüdel; E P Hoffman
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

Review 4.  Guidelines on clinical presentation and management of nondystrophic myotonias.

Authors:  Bas C Stunnenberg; Samantha LoRusso; W David Arnold; Richard J Barohn; Stephen C Cannon; Bertrand Fontaine; Robert C Griggs; Michael G Hanna; Emma Matthews; Giovanni Meola; Valeria A Sansone; Jaya R Trivedi; Baziel G M van Engelen; Savine Vicart; Jeffrey M Statland
Journal:  Muscle Nerve       Date:  2020-05-27       Impact factor: 3.217

5.  Characterization of the high-conductance Ca(2+)-activated K+ channel in adult human skeletal muscle.

Authors:  H Lerche; C Fahlke; P A Iaizzo; F Lehmann-Horn
Journal:  Pflugers Arch       Date:  1995-03       Impact factor: 3.657

6.  Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.

Authors:  J Wang; J Zhou; S M Todorovic; W G Feero; F Barany; R Conwit; I Hausmanowa-Petrusewicz; A Fidzianska; K Arahata; H B Wessel
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

7.  Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels.

Authors:  S C Cannon; R H Brown; D P Corey
Journal:  Biophys J       Date:  1993-07       Impact factor: 4.033

8.  Voltage clamp of rat and human skeletal muscle: measurements with an improved loose-patch technique.

Authors:  W Almers; W M Roberts; R L Ruff
Journal:  J Physiol       Date:  1984-02       Impact factor: 5.182

9.  Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Authors:  L J Ptacek; J S Trimmer; W S Agnew; J W Roberts; J H Petajan; M Leppert
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

10.  Repetitive nerve stimulation in the differential diagnosis of congenital myotonia.

Authors:  B Rossi; A Rossi; F Sartucci
Journal:  Ital J Neurol Sci       Date:  1984-12
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