Literature DB >> 14557559

Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis.

Y Sugiura1, N Makita, L Li, P J Noble, J Kimura, Y Kumagai, T Soeda, T Yamamoto.   

Abstract

BACKGROUND: The authors reported a mutation, P1158S, of the human skeletal muscle sodium channel gene (SCN4A) in a family with cold-induced hypokalemic periodic paralysis (hypoKPP) and myotonia.
OBJECTIVE: To identify mechanisms of temperature dependency in this channelopathy.
METHODS: Using the amphotericin B perforated patch clamp method, sodium currents were recorded at 22 and 32 degrees C from the wild-type (WT) and P1158S mutant SCN4A expressed in tsA201 cells. Computer simulation was performed, incorporating the gating parameters of the P1158S mutant SCN4A.
RESULTS: P1158S mutant SCN4A exhibited hyperpolarizing shifts in voltage dependence of both activation and inactivation curves at a cold temperature and a slower rate of inactivation than the WT. Computer simulation reproduced the abnormal skeletal muscle electrical activities of both paralysis at a low potassium concentration in the cold and myotonia at a normal potassium concentration.
CONCLUSIONS: Both paralysis and myotonia are attributable to the biophysical properties of the SCN4A mutation associated with hypoKPP. This is the first report of an SCN4A mutation that exhibits temperature-dependent shifts of voltage dependence in sodium channel gating.

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Year:  2003        PMID: 14557559     DOI: 10.1212/01.wnl.0000086820.54065.a0

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  15 in total

1.  A nonsense mutation in the SCN9A gene in congenital insensitivity to pain.

Authors:  Mazen Kurban; Muhammad Wajid; Yutaka Shimomura; Angela M Christiano
Journal:  Dermatology       Date:  2010-07-13       Impact factor: 5.366

2.  Paroxysmal extreme pain disorder mutations within the D3/S4-S5 linker of Nav1.7 cause moderate destabilization of fast inactivation.

Authors:  Brian W Jarecki; Patrick L Sheets; James O Jackson; Theodore R Cummins
Journal:  J Physiol       Date:  2008-07-03       Impact factor: 5.182

3.  N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.

Authors:  Qing Ke; Jia Ye; Siyang Tang; Jin Wang; Benyan Luo; Fang Ji; Xu Zhang; Ye Yu; Xiaoyang Cheng; Yuezhou Li
Journal:  J Physiol       Date:  2017-10-15       Impact factor: 5.182

4.  Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians.

Authors:  Juan Zhao; Nicolas Duprè; Jack Puymirat; Mohamed Chahine
Journal:  J Physiol       Date:  2012-01-16       Impact factor: 5.182

5.  Mutations at opposite ends of the DIII/S4-S5 linker of sodium channel Na V 1.7 produce distinct pain disorders.

Authors:  Xiaoyang Cheng; Sulayman D Dib-Hajj; Lynda Tyrrell; Dowain A Wright; Tanya Z Fischer; Stephen G Waxman
Journal:  Mol Pain       Date:  2010-04-29       Impact factor: 3.395

6.  Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.

Authors:  Jadon Webb; Stephen C Cannon
Journal:  Neurology       Date:  2007-09-26       Impact factor: 9.910

Review 7.  Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.

Authors:  Bertrand Fontaine; Emmanuel Fournier; Damien Sternberg; Savine Vicart; Nacira Tabti
Journal:  Neurotherapeutics       Date:  2007-04       Impact factor: 7.620

8.  Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.

Authors:  Thomas Carle; Emmanuel Fournier; Damien Sternberg; Bertrand Fontaine; Nacira Tabti
Journal:  J Physiol       Date:  2009-02-16       Impact factor: 5.182

9.  Skeletal muscle na channel disorders.

Authors:  Dina Simkin; Saïd Bendahhou
Journal:  Front Pharmacol       Date:  2011-10-14       Impact factor: 5.810

10.  Translational approach to address therapy in myotonia permanens due to a new SCN4A mutation.

Authors:  Jean-François Desaphy; Roberta Carbonara; Adele D'Amico; Anna Modoni; Julien Roussel; Paola Imbrici; Serena Pagliarani; Sabrina Lucchiari; Mauro Lo Monaco; Diana Conte Camerino
Journal:  Neurology       Date:  2016-04-29       Impact factor: 9.910

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