Literature DB >> 6304507

Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parameters.

F Lehmann-Horn, R Rüdel, K Ricker, H Lorković, R Dengler, H C Hopf.   

Abstract

Membrane potentials, current-voltage relationships, and contractile parameters were studied in intact muscle cell bundles obtained from two patients with adynamia episodica hereditaria. In a normal extracellular medium, the cell membranes had resting potentials of about -80 mV and their current-voltage relationships were not significantly different from control curves. In contrast to normal muscles the afflicted cells were paralyzed in a medium having 6-10 mmol/liter potassium. The mechanisms of paralysis in the two specimens were different from each other. Many fibers from one patient were spontaneously active even in normal solution. In high potassium solution spontaneous activity was increased and the cells gradually depolarized to values at which excitatory sodium current is normally inactivated. This depolarization was connected with an increased sodium conductance and was reversed by the application of tetrodotoxin (TTX). The fibers from the other patient were not spontaneously active. In high potassium solution they were paralyzed at membrane potential values at which normal fibers would still contract. The reason for this paralysis was a reduced excitability.

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Year:  1983        PMID: 6304507     DOI: 10.1002/mus.880060206

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


  26 in total

Review 1.  Inherited disorders of voltage-gated sodium channels.

Authors:  Alfred L George
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

2.  Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

Authors:  F Lehmann-Horn; P A Iaizzo; H Hatt; C Franke
Journal:  Pflugers Arch       Date:  1991-04       Impact factor: 3.657

3.  Sodium channels gone wild: resurgent current from neuronal and muscle channelopathies.

Authors:  Stephen C Cannon; Bruce P Bean
Journal:  J Clin Invest       Date:  2009-12-28       Impact factor: 14.808

4.  Impaired slow inactivation in mutant sodium channels.

Authors:  T R Cummins; F J Sigworth
Journal:  Biophys J       Date:  1996-07       Impact factor: 4.033

5.  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

6.  Leaky channels make weak muscles.

Authors:  Alfred L George
Journal:  J Clin Invest       Date:  2012-11-26       Impact factor: 14.808

7.  Spontaneous opening at zero membrane potential of sodium channels from eel electroplax reconstituted into lipid vesicles.

Authors:  D S Duch; S R Levinson
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

8.  Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro.

Authors:  N Yang; S Ji; M Zhou; L J Ptácek; R L Barchi; R Horn; A L George
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

9.  Cromakalim (BRL 34915) restores in vitro the membrane potential of depolarized human skeletal muscle fibres.

Authors:  A Spuler; F Lehmann-Horn; P Grafe
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-03       Impact factor: 3.000

10.  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

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