Abstract
How voltage-gated DHP receptor controls the gating of the Ryanodine receptor in cardiac and skeletal muscle has been the central question of E-C coupling over the past two decades. Although the question remains still not fully answered, a number of biochemical, biophysical and molecular observations have furthered and focused the scientific understanding of the problem. In cardiac muscle, the general scheme that has emerged provides a primary role for transmembrane influx of Ca2+, not only in the direct activation of myofilament, but also in gating the release of intracellular Ca2+ stores [1–6].
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Morad, M. (1996). Signaling of calcium release in cardiac muscle. In: Morad, M., Ebashi, S., Trautwein, W., Kurachi, Y. (eds) Molecular Physiology and Pharmacology of Cardiac Ion Channels and Transporters. Developments in Cardiovascular Medicine, vol 182. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3990-8_32
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DOI: https://doi.org/10.1007/978-94-011-3990-8_32
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