%0 Journal Article %1 Alta_2007_590 %A Altamirano, Julio %A Bers, Donald M %D 2007 %J Circ Res %K Action Animals; Caffeine, Calcium Calcium, Cardiac, Channel Channel, Channels, Confocal; Contraction; Electric Gating, Ion Kinetics; L-Type, Membrane Microscopy, Myocardial Myocytes, Patch-Clamp Potentials; Rats; Receptor Release Reticulum, Ryanodine Sarcoplasmic Signaling, Stimulation; Techniques; drug effects/metabolism effects/metabolism; effects; metabolism; pharmacology; %N 6 %P 590--597 %R 10.1161/CIRCRESAHA.107.152322 %T Voltage dependence of cardiac excitation-contraction coupling: unitary Ca2+ current amplitude and open channel probability. %U http://dx.doi.org/10.1161/CIRCRESAHA.107.152322 %V 101 %X Excitation-contraction coupling in cardiac myocytes occurs by Ca2+-induced Ca2+ release, where L-type Ca2+ current evokes a larger sarcoplasmic reticulum (SR) Ca2+ release. The Ca2+-induced Ca2+ release amplification factor or gain (SR Ca2+ release/I(Ca)) is usually assessed by the V(m) dependence of current and Ca2+ transients. Gain rises at negative V(m), as does single channel I(Ca) (i(Ca)), which has led to the suggestion that the increases of i(Ca) amplitude enhances gain at more negative V(m). However, I(Ca) = NP(o) x i(Ca) (where NP(o) is the number of open channels), and NP(o) and i(Ca) both depend on V(m). To assess how i(Ca) and NP(o) separately influence Ca2+-induced Ca2+ release, we measured I(Ca) and junctional SR Ca2+ release in voltage-clamped rat ventricular myocytes using "Ca2+ spikes" (confocal microscopy). To vary i(Ca) alone, we changed Ca2+(o) rapidly at constant test V(m) (0 mV) or abruptly repolarized from +120 mV to different V(m) (at constant Ca2+(o)). To vary NP(o) alone, we altered Ca2+ channel availability by varying holding V(m) (at constant test V(m)). Reducing either i(Ca) or NP(o) alone increased excitation-contraction coupling gain. Thus, increasing i(Ca) does not increase gain at progressively negative test V(m). Such enhanced gain depends on lower NP(o) and reduced redundant Ca2+ channel openings (per junction) and a consequently smaller denominator in the gain equation. Furthermore, modest i(Ca) (at V(m) = 0 mV) may still effectively trigger SR Ca2+ release, whereas at positive V(m) (and smaller i(Ca)), high and well-synchronized channel openings are required for efficient excitation-contraction coupling. At very positive V(m), reduced i(Ca) must explain reduced SR Ca2+ release.

@article{Alta_2007_590, abstract = {Excitation-contraction coupling in cardiac myocytes occurs by Ca2+-induced Ca2+ release, where L-type Ca2+ current evokes a larger sarcoplasmic reticulum (SR) Ca2+ release. The Ca2+-induced Ca2+ release amplification factor or gain (SR Ca2+ release/I(Ca)) is usually assessed by the V(m) dependence of current and Ca2+ transients. Gain rises at negative V(m), as does single channel I(Ca) (i(Ca)), which has led to the suggestion that the increases of i(Ca) amplitude enhances gain at more negative V(m). However, I(Ca) = NP(o) x i(Ca) (where NP(o) is the number of open channels), and NP(o) and i(Ca) both depend on V(m). To assess how i(Ca) and NP(o) separately influence Ca2+-induced Ca2+ release, we measured I(Ca) and junctional SR Ca2+ release in voltage-clamped rat ventricular myocytes using "Ca2+ spikes" (confocal microscopy). To vary i(Ca) alone, we changed [Ca2+](o) rapidly at constant test V(m) (0 mV) or abruptly repolarized from +120 mV to different V(m) (at constant [Ca2+](o)). To vary NP(o) alone, we altered Ca2+ channel availability by varying holding V(m) (at constant test V(m)). Reducing either i(Ca) or NP(o) alone increased excitation-contraction coupling gain. Thus, increasing i(Ca) does not increase gain at progressively negative test V(m). Such enhanced gain depends on lower NP(o) and reduced redundant Ca2+ channel openings (per junction) and a consequently smaller denominator in the gain equation. Furthermore, modest i(Ca) (at V(m) = 0 mV) may still effectively trigger SR Ca2+ release, whereas at positive V(m) (and smaller i(Ca)), high and well-synchronized channel openings are required for efficient excitation-contraction coupling. At very positive V(m), reduced i(Ca) must explain reduced SR Ca2+ release.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {Altamirano, Julio and Bers, Donald M}, biburl = {https://www.bibsonomy.org/bibtex/25bd9ad17ce3a1a53fe15467717e51eca/hake}, description = {The whole bibliography file I use.}, doi = {10.1161/CIRCRESAHA.107.152322}, file = {Alta_2007_590.pdf:Alta_2007_590.pdf:PDF}, institution = {Department of Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 S First Ave, Maywood, IL 60153, USA.}, interhash = {3ab82c4495ba004fe2e85d34d6fd13e6}, intrahash = {5bd9ad17ce3a1a53fe15467717e51eca}, journal = {Circ Res}, keywords = {Action Animals; Caffeine, Calcium Calcium, Cardiac, Channel Channel, Channels, Confocal; Contraction; Electric Gating, Ion Kinetics; L-Type, Membrane Microscopy, Myocardial Myocytes, Patch-Clamp Potentials; Rats; Receptor Release Reticulum, Ryanodine Sarcoplasmic Signaling, Stimulation; Techniques; drug effects/metabolism effects/metabolism; effects; metabolism; pharmacology;}, month = Sep, number = 6, pages = {590--597}, pdf = {Alta_2007_590.pdf}, pii = {CIRCRESAHA.107.152322}, pmid = {17641229}, timestamp = {2009-06-03T11:20:58.000+0200}, title = {Voltage dependence of cardiac excitation-contraction coupling: unitary Ca2+ current amplitude and open channel probability.}, url = {http://dx.doi.org/10.1161/CIRCRESAHA.107.152322}, volume = 101, year = 2007 }