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Research Article Free access | 10.1172/JCI106703
Department of Pharmacology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Find articles by Lipicky, R. in: PubMed | Google Scholar
Department of Pharmacology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Find articles by Bryant, S. in: PubMed | Google Scholar
Department of Pharmacology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio 45219
Find articles by Salmon, J. in: PubMed | Google Scholar
Published October 1, 1971 - More info
In isolated fiber bundles of external intercostal muscle from each of 13 normal volunteers and each of 6 patients with myotonia congenita, some or all of the following were measured: concentrations of Na+, K+, and Cl-, extracellular volume, water content, K+ efflux, fiber size, fiber cable parameters, and fiber resting potentials.
Muscle from patients with myotonia congenita differed significantly (0.001 <P< 0.025) with respect to the following mean values (myotonia congenita vs. normal): the membrane resistance was greater (5729 vs. 2619 ω·cm2), the internal resistivity was less (75.0 vs. 123.2 ω·cm), the water content was less (788.2 vs. 808.2 ml/kg wet weight), and the mean resting potential was greater (68 vs. 61 mv).
No significant differences were found with respect to the following variables: K+ content (73.5 vs. 66.7 mEq/kg wet weight) and the calculated intracellular K+ concentration (215 vs. 191 mEq/liter fiber water), fiber capacitance (5.90 vs. 5.15 μf/cm2), Na+ content (97.7 vs. 94.1 mEq/kg wet weight), Cl- content (79.0 vs. 74.7 mEq/kg wet weight), mannitol extracellular volume (45.1 vs. 46.6 cc/100 g wet weight), and K+ efflux (23.2 vs. 21.5 moles × 10-12 cm-2·sec-1).
These abnormalities of skeletal muscle in human myotonia congenita are like those of skeletal muscle in goats with hereditary myotonia. We tentatively conclude that a decreased Cl- permeability accounts for some of the abnormal electrical properties of skeletal muscle in myotonia congenita.