Abstract
The use of pharmacologic agents as tools to aid in the characterization and separation of physiological processes is not a new idea. The availability of specific toxins like tetrodotoxin and saxitoxin made it easy to test for the presence of sodium channels in excitable cells and made possible the purification(1) reconstitution(2,3) and cloning(4) of such channels. We hope to utilize a pharmacologic approach here to determine whether a Ca2+ -channel isolated recently from skeletal muscle sarcoplasmic reticulum (SR) is the one of physiological importance. Is it the right channel? We know several methods exist to cause Ca2+ release from SR.(5,6) If we had specific inhibitors for each form of release, we could test whether the releases or channels they blocked were involved in excitation-contraction coupling. We will examine the role of Ca2+ -induced Ca2+ release channels first because these are the channels already isolated.
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© 1990 Plenum Press, New York
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Palade, P., Brunder, D., Dettbarn, C., Stein, P. (1990). A Pharmacological Approach to the Physiological Mechanism of Excitation-Contraction Coupling. In: Hidalgo, C., Bacigalupo, J., Jaimovich, E., Vergara, J. (eds) Transduction in Biological Systems. Series of the Centro de Estudios Científicos de Santiago. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5736-0_27
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DOI: https://doi.org/10.1007/978-1-4684-5736-0_27
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