Literature DB >> 10718736

Voltage-dependent Ca2+ release from the SR of feline ventricular myocytes is explained by Ca2+-induced Ca2+ release.

V Piacentino1, K Dipla, J P Gaughan, S R Houser.   

Abstract

1. Direct voltage-gated (voltage-dependent Ca2+ release, VDCR) and Ca2+ influx-gated (Ca2+-induced Ca2+ release, CICR) sarcoplasmic reticulum (SR) Ca2+ release were studied in feline ventricular myocytes. The voltage-contraction relationship predicted by the VDCR hypothesis is sigmoidal with large contractions at potentials near the Ca2+ equilibrium potential (ECa). The relationship predicted by the CICR hypothesis is bell-shaped with no contraction at ECa. 2. The voltage dependence of contraction was measured in ventricular myocytes at physiological temperature (37 C), resting membrane potential and physiological [K+]. Experiments were performed with cyclic adenosine 3',5'-monophosphate (cAMP) in the pipette or in the presence of the beta-adrenergic agonist isoproterenol (isoprenaline; ISO). 3. The voltage-contraction relationship was bell-shaped in Na+-free solutions (to eliminate the Na+ current and Na+-Ca2+ exchange, NCX) but the relationship was broader than the L-type Ca2+ current (ICa,L)-voltage relationship. 4. Contractions induced with voltage steps from normal resting potentials to -40 mV are thought to represent VDCR rather than CICR. We found that cAMP and ISO shifted the voltage dependence of ICa,L activation to more negative potentials so that ICa,L was always present with steps to -40 mV. ICa,L at -40 mV inactivated when the holding potential was decreased (VŁ = -57.8 +/- 0.49 mV). 5. ISO increased inward current, SR Ca2+ load and contraction in physiological [Na+] and a broad bell-shaped voltage-contraction relationship was observed. Inhibition of reverse-mode NCX, decreasing ICa,L and decreasing SR Ca2+ loading all decreased contractions at strongly positive potentials near ECa. 6. The voltage-contraction relationship in 200 microM cadmium (Cd2+) was bell-shaped, supporting a role of ICa,L rather than VDCR. 7. All results could be accounted for by the CICR hypothesis, and many results exclude the VDCR hypothesis.

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Year:  2000        PMID: 10718736      PMCID: PMC2269826          DOI: 10.1111/j.1469-7793.2000.t01-1-00533.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  42 in total

1.  Sodium-calcium exchange-mediated contractions in feline ventricular myocytes.

Authors:  H B Nuss; S R Houser
Journal:  Am J Physiol       Date:  1992-10

2.  Role of Ca2+ channel in cardiac excitation-contraction coupling in the rat: evidence from Ca2+ transients and contraction.

Authors:  L Cleemann; M Morad
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

3.  The control of calcium release in heart muscle.

Authors:  M B Cannell; H Cheng; W J Lederer
Journal:  Science       Date:  1995-05-19       Impact factor: 47.728

4.  Local calcium transients triggered by single L-type calcium channel currents in cardiac cells.

Authors:  J R López-López; P S Shacklock; C W Balke; W G Wier
Journal:  Science       Date:  1995-05-19       Impact factor: 47.728

5.  An estimate of the calcium content of the sarcoplasmic reticulum in rat ventricular myocytes.

Authors:  A Varro; N Negretti; S B Hester; D A Eisner
Journal:  Pflugers Arch       Date:  1993-04       Impact factor: 3.657

6.  Sodium current-induced calcium signals in isolated guinea-pig ventricular myocytes.

Authors:  P Lipp; E Niggli
Journal:  J Physiol       Date:  1994-02-01       Impact factor: 5.182

7.  Sodium current-induced release of calcium from cardiac sarcoplasmic reticulum.

Authors:  N Leblanc; J R Hume
Journal:  Science       Date:  1990-04-20       Impact factor: 47.728

8.  Depolarization-induced Ca entry via Na-Ca exchange triggers SR release in guinea pig cardiac myocytes.

Authors:  A J Levi; K W Spitzer; O Kohmoto; J H Bridge
Journal:  Am J Physiol       Date:  1994-04

9.  Sarcoplasmic reticulum-related changes in cytosolic calcium in pressure-overload-induced feline LV hypertrophy.

Authors:  B A Bailey; S R Houser
Journal:  Am J Physiol       Date:  1993-12

10.  Ca2+ load of guinea-pig ventricular myocytes determines efficacy of brief Ca2+ currents as trigger for Ca2+ release.

Authors:  S Han; A Schiefer; G Isenberg
Journal:  J Physiol       Date:  1994-11-01       Impact factor: 5.182

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  15 in total

1.  A cardiac dihydropyridine receptor II-III loop peptide inhibits resting Ca(2+) sparks in ferret ventricular myocytes.

Authors:  Y Li; D M Bers
Journal:  J Physiol       Date:  2001-11-15       Impact factor: 5.182

Review 2.  Regulation of cardiac excitation-contraction coupling by action potential repolarization: role of the transient outward potassium current (I(to)).

Authors:  Rajan Sah; Rafael J Ramirez; Gavin Y Oudit; Dominica Gidrewicz; Maria G Trivieri; Carsten Zobel; Peter H Backx
Journal:  J Physiol       Date:  2003-01-01       Impact factor: 5.182

3.  Modulation of the Ca(2+)-induced Ca(2+) release cascade by beta-adrenergic stimulation in rat ventricular myocytes.

Authors:  S Viatchenko-Karpinski; S Györke
Journal:  J Physiol       Date:  2001-06-15       Impact factor: 5.182

4.  The inotropic effect of cardioactive glycosides in ventricular myocytes requires Na+-Ca2+ exchanger function.

Authors:  Julio Altamirano; Yanxia Li; Jaime DeSantiago; Valentino Piacentino; Steven R Houser; Donald M Bers
Journal:  J Physiol       Date:  2006-07-06       Impact factor: 5.182

5.  Synergistic interactions between Ca2+ entries through L-type Ca2+ channels and Na+-Ca2+ exchanger in normal and failing rat heart.

Authors:  Serge Viatchenko-Karpinski; Dmitry Terentyev; Leigh Ann Jenkins; Lorenz O Lutherer; Sandor Györke
Journal:  J Physiol       Date:  2005-06-23       Impact factor: 5.182

Review 6.  Role of RyR2 phosphorylation in heart failure and arrhythmias: protein kinase A-mediated hyperphosphorylation of the ryanodine receptor at serine 2808 does not alter cardiac contractility or cause heart failure and arrhythmias.

Authors:  Steven R Houser
Journal:  Circ Res       Date:  2014-04-11       Impact factor: 17.367

7.  Ca2+ influx through T- and L-type Ca2+ channels have different effects on myocyte contractility and induce unique cardiac phenotypes.

Authors:  Naser Jaleel; Hiroyuki Nakayama; Xiongwen Chen; Hajime Kubo; Scott MacDonnell; Hongyu Zhang; Remus Berretta; Jeffrey Robbins; Leanne Cribbs; Jeffery D Molkentin; Steven R Houser
Journal:  Circ Res       Date:  2008-10-02       Impact factor: 17.367

8.  Protein phosphatase 1 and an opposing protein kinase regulate steady-state L-type Ca2+ current in mouse cardiac myocytes.

Authors:  William H duBell; Terry B Rogers
Journal:  J Physiol       Date:  2004-01-23       Impact factor: 5.182

9.  Halothane alters contractility and Ca2+ transport in ventricular myocytes from streptozotocin-induced diabetic rats.

Authors:  Alyson Woodall; Nicolas Bracken; Anwar Qureshi; Frank Christopher Howarth; Jaipaul Singh
Journal:  Mol Cell Biochem       Date:  2004-06       Impact factor: 3.396

10.  Negative inotropic effects of high-mobility group box 1 protein in isolated contracting cardiac myocytes.

Authors:  Huei-Ping Tzeng; Jinping Fan; Jesus G Vallejo; Jian Wen Dong; Xiongwen Chen; Steven R Houser; Douglas L Mann
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-01-25       Impact factor: 4.733

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