Literature DB >> 33488406

Ex vivo Methods for Measuring Cardiac Muscle Mechanical Properties.

Walter E Knight1, Hadi R Ali1, Stephanie J Nakano2, Cortney E Wilson1, Lori A Walker1, Kathleen C Woulfe1.   

Abstract

Cardiovascular disease continues to be the leading cause of morbidity and mortality in the United States and thousands of manuscripts each year are aimed at elucidating mechanisms underlying cardiac disease. The methods for quantifying cardiac performance are quite varied, with each technique assessing unique features of cardiac muscle mechanical properties. Accordingly, in this review, we discuss current ex vivo methods for quantifying cardiac muscle performance, highlighting what can be learned from each method, and how each technique can be used in conjunction to complement others for a more comprehensive understanding of cardiac function. Importantly, cardiac function can be assessed at several different levels, from the whole organ down to individual protein-protein interactions. Here, we take a reductionist view of methods that are commonly used to measure the distinct aspects of cardiac mechanical function, beginning with whole heart preparations and finishing with the in vitro motility assay. While each of the techniques are individually well-documented in the literature, there is a significant need for a comparison of the techniques, delineating the mechanical parameters that can are best measured with each technique, as well as the strengths and weaknesses inherent to each method. Additionally, we will consider complementary techniques and how these methods can be used in combination to improve our understanding of cardiac mechanical function. By presenting each of these methods, with their strengths and limitations, in a single manuscript, this review will assist cardiovascular biologists in understanding the existing literature on cardiac mechanical function, as well as designing future experiments.
Copyright © 2021 Knight, Ali, Nakano, Wilson, Walker and Woulfe.

Entities:  

Keywords:  cardiac muscle; cardiac physiology; contractility and relaxation; mechanical function; myofilament

Year:  2021        PMID: 33488406      PMCID: PMC7820907          DOI: 10.3389/fphys.2020.616996

Source DB:  PubMed          Journal:  Front Physiol        ISSN: 1664-042X            Impact factor:   4.566


  76 in total

1.  The off rate of Ca(2+) from troponin C is regulated by force-generating cross bridges in skeletal muscle.

Authors:  Ying Wang; W Glenn L Kerrick
Journal:  J Appl Physiol (1985)       Date:  2002-06

Review 2.  Calcium, thin filaments, and the integrative biology of cardiac contractility.

Authors:  Tomoyoshi Kobayashi; R John Solaro
Journal:  Annu Rev Physiol       Date:  2005       Impact factor: 19.318

3.  Effect of endothelin as a coronary vasoconstrictor in the Langendorff-perfused rat heart.

Authors:  K Fukuda; S Hori; M Kusuhara; T Satoh; S Kyotani; S Handa; Y Nakamura; H Oono; K Yamaguchi
Journal:  Eur J Pharmacol       Date:  1989-06-20       Impact factor: 4.432

4.  AFos inhibits phenylephrine-mediated contractile dysfunction by altering phospholamban phosphorylation.

Authors:  Mark Y Jeong; John S Walker; R Dale Brown; Russell L Moore; Charles S Vinson; Wilson S Colucci; Carlin S Long
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-04-02       Impact factor: 4.733

5.  Movement of myosin-coated beads on oriented filaments reconstituted from purified actin.

Authors:  J A Spudich; S J Kron; M P Sheetz
Journal:  Nature       Date:  1985 Jun 13-19       Impact factor: 49.962

Review 6.  Mechanical properties of isolated cardiac myocytes.

Authors:  A J Brady
Journal:  Physiol Rev       Date:  1991-04       Impact factor: 37.312

7.  Ratiometric imaging of calcium during ischemia-reperfusion injury in isolated mouse hearts using Fura-2.

Authors:  Raghav Venkataraman; Mark R Holcomb; Rene Harder; Björn C Knollmann; Franz Baudenbacher
Journal:  Biomed Eng Online       Date:  2012-07-19       Impact factor: 2.819

8.  The homozygous K280N troponin T mutation alters cross-bridge kinetics and energetics in human HCM.

Authors:  Nicoletta Piroddi; E Rosalie Witjas-Paalberends; Claudia Ferrara; Cecilia Ferrantini; Giulia Vitale; Beatrice Scellini; Paul J M Wijnker; Vasco Sequiera; Dennis Dooijes; Cristobal Dos Remedios; Saskia Schlossarek; Man Ching Leung; Andrew Messer; Douglas G Ward; Annibale Biggeri; Chiara Tesi; Lucie Carrier; Charles S Redwood; Steven B Marston; Jolanda van der Velden; Corrado Poggesi
Journal:  J Gen Physiol       Date:  2018-12-21       Impact factor: 4.086

9.  A Novel Method of Isolating Myofibrils From Primary Cardiomyocyte Culture Suitable for Myofibril Mechanical Study.

Authors:  Kathleen C Woulfe; Claudia Ferrara; Jose Manuel Pioner; Jennifer H Mahaffey; Raffaele Coppini; Beatrice Scellini; Cecilia Ferrantini; Nicoletta Piroddi; Chiari Tesi; Corrado Poggesi; Mark Jeong
Journal:  Front Cardiovasc Med       Date:  2019-02-19

10.  Quantitative Comparison of Effects of Dofetilide, Sotalol, Quinidine, and Verapamil between Human Ex vivo Trabeculae and In silico Ventricular Models Incorporating Inter-Individual Action Potential Variability.

Authors:  Oliver J Britton; Najah Abi-Gerges; Guy Page; Andre Ghetti; Paul E Miller; Blanca Rodriguez
Journal:  Front Physiol       Date:  2017-08-18       Impact factor: 4.566

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  2 in total

Review 1.  Physiology of the Right Ventricle Across the Lifespan.

Authors:  Kathleen C Woulfe; Lori A Walker
Journal:  Front Physiol       Date:  2021-03-02       Impact factor: 4.566

2.  Sex-specific responses to slow progressive pressure overload in a large animal model of HFpEF.

Authors:  Deborah M Eaton; Remus M Berretta; Jacqueline E Lynch; Joshua G Travers; Ryan D Pfeiffer; Michelle L Hulke; Huaqing Zhao; Alexander R H Hobby; Giana Schena; Jaslyn P Johnson; Markus Wallner; Edward Lau; Maggie P Y Lam; Kathleen C Woulfe; Nathan R Tucker; Timothy A McKinsey; Marla R Wolfson; Steven R Houser
Journal:  Am J Physiol Heart Circ Physiol       Date:  2022-09-02       Impact factor: 5.125

  2 in total

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