Multiscale modeling in rodent ventricular myocytes

This paper indicates that in ventricular myocytes when the SR (sarcoplasmic reticulum) is pharmacologically inhibited, the intracellular Ca²⁺concentration rapidly increases during Ca²⁺ entrance (0-70 ms), whereas the decay of Ca²⁺ is slow; in the absence of fluorescent dye, large Ca²⁺ concentration gradients might develop near the cell membrane; intracellular Ca²⁺ distribution is tightly regulated by the localization of Ca²⁺transporter proteins along the sarcolemma and strongly relays on the presence of mobile and stationary Ca²⁺ buffers. These studies also imply that in ventricular cells with intact and functional SR, the Ca²⁺ signal most likely would spread faster along the t-tubular system, surface membrane than to the cell interior and that in the absence of Ca²⁺ dye high Ca²⁺ gradients under the surface membrane and more uniform Ca²⁺ distribution in the cell interior might be expected.