Literature DB >> 20852049

Myocardial contraction-relaxation coupling.

Paul M L Janssen1.   

Abstract

Since the pioneering work of Henry Pickering Bowditch in the late 1800s to early 1900s, cardiac muscle contraction has remained an intensely studied topic for several reasons. The heart is located centrally in our body, and its pumping motion demands the attention of the observer. The contraction of the heart encompasses a complex interplay of mechanical, chemical, and electrical properties, and its function can thus be studied from any of these viewpoints. In addition, diseases of the heart are currently killing more people in the Westernized world than any other disease. When combined with the increasing emphasis of research to be clinically relevant, this contributes to the heart remaining a topic of continued basic and clinical investigation. Yet, there are significant aspects of cardiac muscle contraction that are still not well understood. A big complication of the study of cardiac muscle contraction is that there exists no equilibrium among many of the important governing parameters, which include pre- and afterload, intracellular ion concentrations, membrane potential, and velocity and direction of movement. Thus the classic approach of perturbing an equilibrium or a steady state to learn about the role of the perturbing factor in the system cannot be unambiguously interpreted, since each of the parameters that govern contraction are constantly changing, as well as constantly changing their interaction with each other. In this review, presented as the 54th Bowditch Lecture at Experimental Biology meeting in Anaheim in April 2010, I will revisit several governing factors of cardiac muscle relaxation by applying newly developed tools and protocols to isolated cardiac muscle tissue in which the dynamic interactions between the governing factors of contraction and relaxation can be studied.

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Mesh:

Year:  2010        PMID: 20852049      PMCID: PMC3006276          DOI: 10.1152/ajpheart.00759.2010

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  56 in total

1.  Cooperative activation in cardiac muscle: impact of sarcomere length.

Authors:  David P Dobesh; John P Konhilas; Pieter P de Tombe
Journal:  Am J Physiol Heart Circ Physiol       Date:  2002-03       Impact factor: 4.733

2.  Increased phosphorylation of tropomyosin, troponin I, and myosin light chain-2 after stretch in rabbit ventricular myocardium under physiological conditions.

Authors:  Michelle M Monasky; Brandon J Biesiadecki; Paul M L Janssen
Journal:  J Mol Cell Cardiol       Date:  2010-03-16       Impact factor: 5.000

3.  Phosphorylation of troponin I and phospholamban during catecholamine stimulation of rabbit heart.

Authors:  E G Kranias; R J Solaro
Journal:  Nature       Date:  1982-07-08       Impact factor: 49.962

4.  Tension development and sarcomere length in rat cardiac trabeculae. Evidence of length-dependent activation.

Authors:  H E ter Keurs; W H Rijnsburger; R van Heuningen; M J Nagelsmit
Journal:  Circ Res       Date:  1980-05       Impact factor: 17.367

5.  The effects of muscle length on intracellular calcium transients in mammalian cardiac muscle.

Authors:  D G Allen; S Kurihara
Journal:  J Physiol       Date:  1982-06       Impact factor: 5.182

6.  Kinetics of cardiac muscle contraction and relaxation are linked and determined by properties of the cardiac sarcomere.

Authors:  Paul M L Janssen
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-07-23       Impact factor: 4.733

7.  Frequency-dependent acceleration of relaxation in the heart depends on CaMKII, but not phospholamban.

Authors:  Jaime DeSantiago; Lars S Maier; Donald M Bers
Journal:  J Mol Cell Cardiol       Date:  2002-08       Impact factor: 5.000

8.  Role of cardiac myosin binding protein C in sustaining left ventricular systolic stiffening.

Authors:  Bradley M Palmer; Dimitrios Georgakopoulos; Paul M Janssen; Yuan Wang; Norman R Alpert; Diego F Belardi; Samantha P Harris; Richard L Moss; Patrick G Burgon; Christine E Seidman; J G Seidman; David W Maughan; David A Kass
Journal:  Circ Res       Date:  2004-04-01       Impact factor: 17.367

9.  Physiological determinants of contractile force generation and calcium handling in mouse myocardium.

Authors:  Linda B Stull; Michelle K Leppo; Eduardo Marbán; Paul M L Janssen
Journal:  J Mol Cell Cardiol       Date:  2002-10       Impact factor: 5.000

10.  Stretch-dependent slow force response in isolated rabbit myocardium is Na+ dependent.

Authors:  Dirk von Lewinski; Burkhard Stumme; Lars S Maier; Claus Luers; Donald M Bers; Burkert Pieske
Journal:  Cardiovasc Res       Date:  2003-03-15       Impact factor: 10.787

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  45 in total

1.  Effects of increased preload on the force-frequency response and contractile kinetics in early stages of cardiac muscle hypertrophy.

Authors:  Kaylan M Haizlip; Tepmanas Bupha-Intr; Brandon J Biesiadecki; Paul M L Janssen
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-03-30       Impact factor: 4.733

Review 2.  Designing proteins to combat disease: Cardiac troponin C as an example.

Authors:  Jonathan P Davis; Vikram Shettigar; Svetlana B Tikunova; Sean C Little; Bin Liu; Jalal K Siddiqui; Paul M L Janssen; Mark T Ziolo; Shane D Walton
Journal:  Arch Biochem Biophys       Date:  2016-02-18       Impact factor: 4.013

3.  Tropomyosin Ser-283 pseudo-phosphorylation slows myofibril relaxation.

Authors:  Benjamin R Nixon; Bin Liu; Beatrice Scellini; Chiara Tesi; Nicoletta Piroddi; Ozgur Ogut; R John Solaro; Mark T Ziolo; Paul M L Janssen; Jonathan P Davis; Corrado Poggesi; Brandon J Biesiadecki
Journal:  Arch Biochem Biophys       Date:  2012-12-08       Impact factor: 4.013

4.  Effects of increased systolic Ca²⁺ and phospholamban phosphorylation during β-adrenergic stimulation on Ca²⁺ transient kinetics in cardiac myocytes.

Authors:  Steve R Roof; Thomas R Shannon; Paul M L Janssen; Mark T Ziolo
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-07-15       Impact factor: 4.733

5.  Stretching single titin molecules from failing human hearts reveals titin's role in blunting cardiac kinetic reserve.

Authors:  Mei-Pian Chen; Salome A Kiduko; Nancy S Saad; Benjamin D Canan; Ahmet Kilic; Peter J Mohler; Paul M L Janssen
Journal:  Cardiovasc Res       Date:  2020-01-01       Impact factor: 10.787

Review 6.  Electromechanical coupling in the cardiac myocyte; stretch-arrhythmia feedback.

Authors:  Henk E D J ter Keurs
Journal:  Pflugers Arch       Date:  2011-03-04       Impact factor: 3.657

7.  Acute volume loading exacerbates direct ventricular interaction in a model of COPD.

Authors:  William S Cheyne; Alexandra M Williams; Megan I Harper; Neil D Eves
Journal:  J Appl Physiol (1985)       Date:  2017-07-20

8.  Automated analysis of contractile force and Ca2+ transients in engineered heart tissue.

Authors:  Andrea Stoehr; Christiane Neuber; Christina Baldauf; Ingra Vollert; Felix W Friedrich; Frederik Flenner; Lucie Carrier; Alexandra Eder; Sebastian Schaaf; Marc N Hirt; Bülent Aksehirlioglu; Carl W Tong; Alessandra Moretti; Thomas Eschenhagen; Arne Hansen
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-02-28       Impact factor: 4.733

9.  Point mutations in the tri-helix bundle of the M-domain of cardiac myosin binding protein-C influence systolic duration and delay cardiac relaxation.

Authors:  Sabine J van Dijk; Kristina B Kooiker; Nathaniel C Napierski; Katia D Touma; Stacy Mazzalupo; Samantha P Harris
Journal:  J Mol Cell Cardiol       Date:  2018-05-03       Impact factor: 5.000

10.  Decrease in sarcoplasmic reticulum calcium content, not myofilament function, contributes to muscle twitch force decline in isolated cardiac trabeculae.

Authors:  Nima Milani-Nejad; Lucia Brunello; Sándor Gyorke; Paul M L Janssen
Journal:  J Muscle Res Cell Motil       Date:  2014-07-24       Impact factor: 2.698

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