Skip to main content
. Author manuscript; available in PMC: 2015 Apr 22.
Published in final edited form as: Curr Drug Targets. 2011 May;12(5):737–747. doi: 10.2174/138945011795378559

Fig. 1.

Fig. 1

Role of NCX in cellular Ca2+ cycling during excitation-contraction coupling in cardiac myocytes. During the action potential Ca2+ enters the myocyte via the voltage dependent sarcolemmal L-type Ca2+ channel, and thus triggers further Ca2+ release from the sarcoplasmic reticulum via sarcoplasmic Ca2+ release channels (ryanodine receptors). The released Ca2+ diffuses towards the myofilaments and induces the contraction. During diastole Ca2+ is shifted back into sarcoplasmic reticulum by the Ca2+ ATPase of the sarcoplasmic reticulum (SERCA). The Na+/Ca2+ exchanger extrudes Ca2+ from the cytosol into the extracellular space.