Protocol

Characterizing the Trigger for Sarcoplasmic Reticulum Ca2+ Release in Cardiac Myocytes

  1. Karin R. Sipido1,4
  1. 1Division of Experimental Cardiology, Department of Cardiovascular Sciences, KU Leuven, Belgium
    • 2 Present address: Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow G12 8TA, United Kingdom.

    • 3 Present address: Biomedical Research Institute, Hasselt University, Agoralaan, 3590 Diepenbeek, Belgium.

    Abstract

    Here, we describe a method for characterizing the L-type Ca2+ current, ICaL, which is a major trigger for Ca2+ release from the sarcoplasmic reticulum (SR). The protocol includes measuring ICaL amplitude and voltage dependence and the elicited SR Ca2+ release. The procedure for measuring ICaL activity is performed using solutions (internal and external) and voltage control such that other ionic currents are eliminated. The resultant relationship between the Ca2+ current and the associated internal [Ca2+]i transient is a first approach for evaluating coupling gain. We discuss which parameters are most appropriate for this analysis and how an evaluation of gain needs to be further explored by measuring the SR Ca2+ content.

    Footnotes

    • 4 Correspondence: karin.sipido{at}med.kuleuven.be

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