%0 Journal Article %1 Cann_1995_1045 %A Cannell, M. B. %A Cheng, H. %A Lederer, W. J. %D 1995 %J Science %K 7754384 Animals, Calcium Calcium, Channel Channel, Channels, Confocal, Ga, Gov't, In Ion Membrane Microscopy, Muscle Myocardium, Non-U.S. P.H.S., Patch-Clamp Potentials, Probability, Proteins, Rats, Receptor Release Research Reticulum, Ryanodine Sarcoplasmic Support, Techniques, U.S. Vitro, ting, %N 5213 %P 1045--1049 %T The control of calcium release in heart muscle. %V 268 %X The control of calcium release from intracellular stores (the sarcoplasmic reticulum) in cardiac muscle was examined with the use of a confocal microscope and voltage clamp techniques. Depolarization evoked graded calcium release by altering the extent of spatial and temporal summation of elementary calcium release events called "calcium sparks." These evoked sparks were triggered by local L-type calcium channel currents in a stochastic manner, were similar at different potentials, and resembled spontaneous calcium sparks. Once triggered, the calcium release from the sarcoplasmic reticulum during a calcium spark was independent of the duration of the triggering calcium influx. These results were used to develop a unifying model for cardiac excitation-contraction coupling that explains the large (but paradoxically stable) amplification of the trigger calcium influx by a combination of digital and analog behavior.

@article{Cann_1995_1045, abstract = {The control of calcium release from intracellular stores (the sarcoplasmic reticulum) in cardiac muscle was examined with the use of a confocal microscope and voltage clamp techniques. Depolarization evoked graded calcium release by altering the extent of spatial and temporal summation of elementary calcium release events called "calcium sparks." These evoked sparks were triggered by local L-type calcium channel currents in a stochastic manner, were similar at different potentials, and resembled spontaneous calcium sparks. Once triggered, the calcium release from the sarcoplasmic reticulum during a calcium spark was independent of the duration of the triggering calcium influx. These results were used to develop a unifying model for cardiac excitation-contraction coupling that explains the large (but paradoxically stable) amplification of the trigger calcium influx by a combination of digital and analog behavior.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {Cannell, M. B. and Cheng, H. and Lederer, W. J.}, biburl = {https://www.bibsonomy.org/bibtex/2f314f7d98fc7ff38e45beba50499ad68/hake}, description = {The whole bibliography file I use.}, file = {Cann_1995_1045.pdf:Cann_1995_1045.pdf:PDF}, interhash = {69c8ae3f6a43c746f6f801a6d486223b}, intrahash = {f314f7d98fc7ff38e45beba50499ad68}, journal = {Science}, keywords = {7754384 Animals, Calcium Calcium, Channel Channel, Channels, Confocal, Ga, Gov't, In Ion Membrane Microscopy, Muscle Myocardium, Non-U.S. P.H.S., Patch-Clamp Potentials, Probability, Proteins, Rats, Receptor Release Research Reticulum, Ryanodine Sarcoplasmic Support, Techniques, U.S. Vitro, ting,}, month = May, number = 5213, pages = {1045--1049}, pmid = {7754384}, timestamp = {2009-06-03T11:21:07.000+0200}, title = {The control of calcium release in heart muscle.}, volume = 268, year = 1995 }