Literature DB >> 1724293

Ionic transporting systems of skeletal muscle in relation with innervation and their involvement in myotonic diseases.

J F Renaud1.   

Abstract

Excitation-contraction coupling describes the series of events that begins with propagated action potential on the muscle fiber surface membrane and leads to the twitch contraction of the fiber. The generation of an action potential during excitation requires rapid sequential changes in membrane conductances of Na+, Ca2+, and K+ ions that depend upon the opening and closing of the respective channels. Myotonic disorders are inherited diseases whose clinical manifestations include electrophysiological signs such as increased excitability and delayed relaxation of the muscles after voluntary contraction. All these disorders appears to be due to an abnormality of the muscle itself since they persist after section or blocking of the motor nerve after curarization. Most experimental and clinical data suggest that human myotonia arises from genetically-induced structural and functional alterations of the muscle membrane. The purpose of this article is to focus on the more recent developments in the molecular and pharmacological analysis of cation transporting systems such as ionic channels and (Na+, K+) ATPase in myotonic disorders.

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Year:  1991        PMID: 1724293     DOI: 10.1007/bf00965553

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  29 in total

Review 1.  Excitation-contraction coupling in skeletal muscle.

Authors:  J Caillé; M Ildefonse; O Rougier
Journal:  Prog Biophys Mol Biol       Date:  1985       Impact factor: 3.667

Review 2.  Appearance and function of voltage-dependent Ca2+ channels during pre- and postnatal development of cardiac and skeletal muscles.

Authors:  J F Renaud; M Fosset; T Kazazoglou; M Lazdunski; A Schmid
Journal:  Ann N Y Acad Sci       Date:  1989       Impact factor: 5.691

3.  Action potential generation in denervated rat skeletal muscle. II. The action of tetrodotoxin.

Authors:  P Redfern; S Thesleff
Journal:  Acta Physiol Scand       Date:  1971-05

4.  Ion content, potassium efflux and cable properties of myotonic, human, external-intercostal muscle.

Authors:  R J Lipicky; S H Bryant
Journal:  Trans Am Neurol Assoc       Date:  1971

5.  Myogenic differentiation in permanent clonal mouse myoblast cell lines: regulation by macromolecular growth factors in the culture medium.

Authors:  T A Linkhart; C H Clegg; S D Hauschika
Journal:  Dev Biol       Date:  1981-08       Impact factor: 3.582

6.  Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy.

Authors:  J F Renaud; C Desnuelle; H Schmid-Antomarchi; M Hugues; G Serratrice; M Lazdunski
Journal:  Nature       Date:  1986 Feb 20-26       Impact factor: 49.962

Review 7.  Biochemistry of muscle membranes in Duchenne muscular dystrophy.

Authors:  L P Rowland
Journal:  Muscle Nerve       Date:  1980 Jan-Feb       Impact factor: 3.217

8.  Sodium channel and sodium pump in normal and pathological muscles from patients with myotonic muscular dystrophy and lower motor neuron impairment.

Authors:  C Desnuelle; A Lombet; G Serratrice; M Lazdunski
Journal:  J Clin Invest       Date:  1982-02       Impact factor: 14.808

9.  Cultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties.

Authors:  M Merickel; R Gray; P Chauvin; S Appel
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

10.  The stoicheiometry of the sodium pump.

Authors:  P J Garrahan; I M Glynn
Journal:  J Physiol       Date:  1967-09       Impact factor: 5.182

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