saxitoxin and Myotonic-Dystrophy

saxitoxin has been researched along with Myotonic-Dystrophy* in 1 studies

Other Studies

1 other study(ies) available for saxitoxin and Myotonic-Dystrophy

Article	Year
Effects of age and gene dose on skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase. Muscle & nerve, 2002, Volume: 25, Issue:6 Myotonic muscular dystrophy (DM) is characterized by abnormal skeletal muscle Na channel gating and reduced levels of myotonic dystrophy protein kinase (DMPK). Electrophysiological measurements show that mice deficient in Dmpk have reduced Na currents in muscle. We now find that the Na channel expression level is normal in mouse muscle partially or completely deficient in Dmpk. Reduced current amplitudes are not changed by age or gene dose, and the reduction is not due to changes in macroscopic or microscopic gating kinetics. The mechanism of abnormal membrane excitability in DM may in part be silencing of muscle Na channels due to Dmpk deficiency. Topics: Aging; Animals; Cell Separation; Disease Models, Animal; Gene Dosage; In Vitro Techniques; Ion Channel Gating; Kinetics; Membrane Potentials; Mice; Mice, Inbred Strains; Mice, Knockout; Muscle, Skeletal; Myotonic Dystrophy; Myotonin-Protein Kinase; Patch-Clamp Techniques; Protein Serine-Threonine Kinases; Radioligand Assay; Saxitoxin; Sodium Channels	2002

Article

Year

Effects of age and gene dose on skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase.

Muscle & nerve, 2002, Volume: 25, Issue:6

Myotonic muscular dystrophy (DM) is characterized by abnormal skeletal muscle Na channel gating and reduced levels of myotonic dystrophy protein kinase (DMPK). Electrophysiological measurements show that mice deficient in Dmpk have reduced Na currents in muscle. We now find that the Na channel expression level is normal in mouse muscle partially or completely deficient in Dmpk. Reduced current amplitudes are not changed by age or gene dose, and the reduction is not due to changes in macroscopic or microscopic gating kinetics. The mechanism of abnormal membrane excitability in DM may in part be silencing of muscle Na channels due to Dmpk deficiency.

Topics: Aging; Animals; Cell Separation; Disease Models, Animal; Gene Dosage; In Vitro Techniques; Ion Channel Gating; Kinetics; Membrane Potentials; Mice; Mice, Inbred Strains; Mice, Knockout; Muscle, Skeletal; Myotonic Dystrophy; Myotonin-Protein Kinase; Patch-Clamp Techniques; Protein Serine-Threonine Kinases; Radioligand Assay; Saxitoxin; Sodium Channels

2002