Literature DB >> 1649995

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

F Lehmann-Horn1, P A Iaizzo, H Hatt, C Franke.   

Abstract

Electrophysiological studies on muscle fibres from patients with hyperkalemic periodic paralysis with myotonia have shown that the episodes of weakness are caused by a sustained depolarization of the sarcolemma to potentials between -40 and -60 mV. In muscle fibre segments from three such patients this sustained depolarization was caused by noninactivating Na+ channels with reduced single-channel conductance blocked by TTX and procainamide. As the chloride conductance was normal, myotonia may be best explained with the abnormal reopenings of the Na+ channels. The recently described genetic linkage between hyperkalemic periodic paralysis with myotonia and the gene coding for the TTX-sensitive Na+ channel suggests an altered primary structure of this channel causing its abnormal function.

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Year:  1991        PMID: 1649995     DOI: 10.1007/bf00370530

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  7 in total

1.  [Not Available].

Authors:  I GAMSTORP
Journal:  Acta Paediatr Suppl       Date:  1956-05

2.  Hyperkalemic periodic paralysis in horses.

Authors:  S J Spier; G P Carlson; T A Holliday; G H Cardinet; J G Pickar
Journal:  J Am Vet Med Assoc       Date:  1990-10-15       Impact factor: 1.936

3.  Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Authors:  B Fontaine; T S Khurana; E P Hoffman; G A Bruns; J L Haines; J A Trofatter; M P Hanson; J Rich; H McFarlane; D M Yasek
Journal:  Science       Date:  1990-11-16       Impact factor: 47.728

4.  Characteristics of single Na+ channels of adult human skeletal muscle.

Authors:  C Franke; H Hatt
Journal:  Pflugers Arch       Date:  1990-01       Impact factor: 3.657

5.  Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH.

Authors:  F Lehmann-Horn; G Küther; K Ricker; P Grafe; K Ballanyi; R Rüdel
Journal:  Muscle Nerve       Date:  1987-05       Impact factor: 3.217

6.  Resealed fiber segments for the study of the pathophysiology of human skeletal muscle.

Authors:  F Lehmann-Horn; P A Iaizzo
Journal:  Muscle Nerve       Date:  1990-03       Impact factor: 3.217

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

Authors:  F Lehmann-Horn; R Rüdel; K Ricker; H Lorković; R Dengler; H C Hopf
Journal:  Muscle Nerve       Date:  1983-02       Impact factor: 3.217

  7 in total
  18 in total

Review 1.  Periodic paralysis: understanding channelopathies.

Authors:  Frank Lehmann-Horn; Karin Jurkat-Rott; Reinhardt Rüdel
Journal:  Curr Neurol Neurosci Rep       Date:  2002-01       Impact factor: 5.081

2.  Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V.

Authors:  Bahram Mohammadi; Nenad Mitrovic; Frank Lehmann-Horn; Reinhard Dengler; Johannes Bufler
Journal:  J Physiol       Date:  2003-01-24       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

4.  Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17.

Authors:  M C Koch; K Ricker; M Otto; T Grimm; E P Hoffman; R Rüdel; K Bender; B Zoll; P S Harper; F Lehmann-Horn
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

5.  Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel.

Authors:  N Mitrović; A L George; H Lerche; S Wagner; C Fahlke; F Lehmann-Horn
Journal:  J Physiol       Date:  1995-08-15       Impact factor: 5.182

6.  Responsiveness of cardiac Na+ channels to a site-directed antiserum against the cytosolic linker between domains III and IV and their sensitivity to other modifying agents.

Authors:  W Beck; I Benz; W Bessler; G Jung; M Kohlhardt
Journal:  J Membr Biol       Date:  1993-06       Impact factor: 1.843

7.  K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation.

Authors:  N Mitrović; A L George; R Heine; S Wagner; U Pika; U Hartlaub; M Zhou; H Lerche; C Fahlke; F Lehmann-Horn
Journal:  J Physiol       Date:  1994-08-01       Impact factor: 5.182

8.  Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis.

Authors:  S C Cannon; D P Corey
Journal:  J Physiol       Date:  1993-07       Impact factor: 5.182

9.  Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker.

Authors:  H Lerche; R Heine; U Pika; A L George; N Mitrovic; M Browatzki; T Weiss; M Rivet-Bastide; C Franke; M Lomonaco
Journal:  J Physiol       Date:  1993-10       Impact factor: 5.182

10.  The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11.

Authors:  C Ambrose; S Cheng; B Fontaine; J H Nadeau; M MacDonald; J F Gusella
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

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