Objective : The H9c2 clonal cell line derived from embryonic rat ventricle is an in vitro surrogate for both cardiac and skeletal myocytes. We recorded Ca
2+ channel currents from cell-attached patches on H9c2 cells in the myotube stage with the aim of better understanding the effect of isoproterenol on skeletal muscle L-type Ca
2+ channel currents.
Methods : Experiments were carried out using myotubules cultured for 15-50 days. Single L-type Ca
2+ channel currents were recorded from cell-attached patches using 100 mM Ba
2+ as the charge carrier in the presence of (+) -202-791, a pure dihydropyridine Ca
2+ channel agonist.
Results : Single L-type Ca
2+ channel currents exhibited long open times with small (skeletal muscle) and large (cardiac) unitary amplitudes. Skeletal muscle L-type channel currents appeared more often than the cardiac channels, and the respective mean currents, which were obtained separately from patches containing both channel types, showed the skeletal muscle current rose more slowly than the cardiac current. Application of 1μ M isoproterenol increased the number of openings of both channel types. In a patch that contained numerous skeletal L-type type channels, isoproterenol increased the maximal amplitude in the current-voltage (I-V) relationship of averaged L-type Ba
2+ currents and shifted the I-V curve towards more negative potentials.
Conclusion : Skeletal L-type Ca
2+ channels are more abundant than cardiac-type channels in H9c2 myotubes. Isoproterenola β-adrenergic agonist, increased openings in the skeletal L-type Ca
2+ channels and their averaged currents as in the cardiac L-type Ca
2+ channels in ventricular myocytes.
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