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J Physiol Volume 577, Number 1, 281-293, November 15, 2006 DOI: 10.1113/jphysiol.2006.117242
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CARDIOVASCULAR

Cytosolic energy reserves determine the effect of glycolytic sugar phosphates on sarcoplasmic reticulum Ca2+ release in cat ventricular myocytes

Aleksey V. Zima1, Jens Kockskämper1 and Lothar A. Blatter1

1 Department of Physiology, Stritch School of Medicine, Loyola University Chicago, 2160 South First Avenue, Maywood, IL 60153, USA

Localization of glycolytic enzymes in close proximity to Ca2+ transport systems of the sarcoplasmic reticulum (SR) in cardiac cells suggests an important functional role for glycolysis in intracellular [Ca2+] regulation and, consequently, excitation–contraction coupling. Here, we investigated the mechanisms of regulation of SR Ca2+ release by glycolytic sugar phosphate intermediates in cat ventricular myocytes. Experiments with permeabilized myocytes revealed that with normal cytosolic energy reserves (mM: ATP 5, ADP 0.01, phosphocreatine (CrP) 10) fructose-1,6-bisphosphate (FBP; 1 mM) and fructose-6-phosphate (F6P; 1 mM) caused a transient increase of Ca2+ spark frequency by 62 and 42%, respectively. This effect of sugar phosphates was associated with a 13% decrease in SR Ca2+ load. Pretreatment of the cells with an inhibitor of glycolysis, iodoacetate (IAA; 0.5 mM), did not prevent the effects of FBP and F6P on Ca2+ sparks. Recording of single ryanodine receptor (RyR) channel activity indicated that FBP and F6P significantly increased RyR open probability. Reduction of cytosolic energy reserves decreased Ca2+ spark activity. Increasing [ADP] to 0.4 mM or removal of CrP ([ATP] was kept constant) caused a slowly developing decrease of Ca2+ spark frequency by 29 and 42%, respectively. Changing [ADP] and [CrP] simultaneously decreased Ca2+ spark frequency by 66%. This inhibition of Ca2+ sparks was associated with a 40% decrease in SR Ca2+ load. The subsequent addition of FBP (1 mM) partially restored Ca2+ spark frequency and SR Ca2+ load. This recovery of Ca2+ sparks was blocked completely by IAA. These data suggest that at physiological ATP, ADP and CrP levels accumulation of sugar phosphates from glycolysis can stimulate SR Ca2+ release. This effect does not require the activity of downstream glycolytic enzymes, but rather is the result of direct activation of RyRs. However, under conditions associated with depletion of cellular energy reserves (e.g. myocardial ischaemia), ATP generated from glycolysis may play an important role in maintaining myocardial Ca2+ homeostasis by improving SR Ca2+ uptake.

(Received 14 July 2006; accepted after revision 29 August 2006; first published online 31 August 2006)
Corresponding author L. A. Blatter: Department of Physiology, Stritch School of Medicine, Loyola University Chicago, 2160 South First Avenue, Maywood, IL 60153, USA. Email: lblatte{at}lumc.edu




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