Literature DB >> 8631764

Measurement of free Ca2+ in sarcoplasmic reticulum in perfused rabbit heart loaded with 1,2-bis(2-amino-5,6-difluorophenoxy)ethane-N,N,N',N'-tetraacetic acid by 19F NMR.

W Chen1, C Steenbergen, L A Levy, J Vance, R E London, E Murphy.   

Abstract

Measurements of free calcium ion concentration in the sarcoplasmic reticulum ([Ca2+]SR) and an evaluation of its relationship to changes in cytosolic free calcium and energy state of the cell, as well as heterogeneity of the SR calcium pool, were performed using 19F NMR in Langendorff perfused rabbit hearts loaded with acetoxymethyl ester of 1,2-bis(2-amino-5,6-difluorophenoxy)ethane-N,N,N',N'-tetraacetic acid. We report a base-line time-average [Ca2+]SR value of 1.5 mM (n = 13) in the beating heart, similar to the value measured at diastole. We further report that [Ca2+]SR decreases by approximately 30% at the start of systole and that there is no evidence of spacial heterogeneity in [Ca2+]SR during the contraction cycle. However, there appears to be a heterogeneous response to SR calcium channel release activator (caffeine) and SR calcium-ATPase inhibitor (cyclopiazonic acid), consistent with studies suggesting that there are subpopulations of SR. Raising cytosolic free calcium by depolarizing the cell with 30 mM extracellular KCl, resulted in an increase in [Ca2+]SR; however, the calcium gradient was unchanged. Lowering cell phosphorylation potential, which would reduce the free energy available for the SR Ca2+-ATPase, leads to a decrease in the calcium gradient across the SR, but this reduced gradient was primarily due to an increase in cytosolic free calcium and not a net release of SR calcium.

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Year:  1996        PMID: 8631764

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  26 in total

1.  The role of luminal Ca2+ in the generation of Ca2+ waves in rat ventricular myocytes.

Authors:  V Lukyanenko; S Subramanian; I Gyorke; T F Wiesner; S Gyorke
Journal:  J Physiol       Date:  1999-07-01       Impact factor: 5.182

2.  The use of the indicator fluo-5N to measure sarcoplasmic reticulum calcium in single muscle fibres of the cane toad.

Authors:  A A Kabbara; D G Allen
Journal:  J Physiol       Date:  2001-07-01       Impact factor: 5.182

Review 3.  Deconstructing calsequestrin. Complex buffering in the calcium store of skeletal muscle.

Authors:  Leandro Royer; Eduardo Ríos
Journal:  J Physiol       Date:  2009-04-29       Impact factor: 5.182

4.  Regulation of the cardiac ryanodine receptor channel by luminal Ca2+ involves luminal Ca2+ sensing sites.

Authors:  I Györke; S Györke
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

5.  Depletion of Ca2+ from the sarcoplasmic reticulum of cardiac muscle prompts phosphorylation of phospholamban to stimulate store refilling.

Authors:  M S Bhogal; J Colyer
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

6.  Assessment of intra-SR free [Ca] and buffering in rat heart.

Authors:  T R Shannon; D M Bers
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

7.  Sarcoplasmic reticulum Ca2+ release flux underlying Ca2+ sparks in cardiac muscle.

Authors:  L A Blatter; J Hüser; E Ríos
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

8.  Calcium release flux underlying Ca2+ sparks of frog skeletal muscle.

Authors:  E Ríos; M D Stern; A González; G Pizarro; N Shirokova
Journal:  J Gen Physiol       Date:  1999-07       Impact factor: 4.086

9.  Unitary Ca2+ current through mammalian cardiac and amphibian skeletal muscle ryanodine receptor Channels under near-physiological ionic conditions.

Authors:  Claudia Kettlun; Adom González; Eduardo Ríos; Michael Fill
Journal:  J Gen Physiol       Date:  2003-09-15       Impact factor: 4.086

Review 10.  Mitochondria in cardiomyocyte Ca2+ signaling.

Authors:  Valeriy Lukyanenko; Aristide Chikando; W J Lederer
Journal:  Int J Biochem Cell Biol       Date:  2009-04-02       Impact factor: 5.085

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