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Experimental Models of Cardiovascular Diseases

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Cover of 'Experimental Models of Cardiovascular Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Experimental Models of Cardiovascular Diseases: Overview
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    Chapter 2 An Introduction to Computational Modeling of Cardiac Electrophysiology and Arrhythmogenicity
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    Chapter 3 Isolation of Atrial and Ventricular Cardiomyocytes for In Vitro Studies
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    Chapter 4 Cardiomyocyte Differentiation from Mouse Embryonic Stem Cells
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    Chapter 5 Cardiomyocyte Differentiation from Human Embryonic Stem Cells
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    Chapter 6 Induction of Human Induced Pluripotent Stem Cells to Cardiomyocytes Using Embryoid Bodies
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    Chapter 7 Measuring Cardiomyocyte Contractility and Calcium Handling In Vitro
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    Chapter 8 Langendorff Perfusion Method as an Ex Vivo Model to Evaluate Heart Function in Rats
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    Chapter 9 Methods for the Preparation of an Excised, Cross-Circulated Rat Heart
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    Chapter 10 Optical Action Potential Mapping in Acute Models of Ischemia–Reperfusion Injury: Probing the Arrhythmogenic Role of the Mitochondrial Translocator Protein
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    Chapter 11 Cardiac Tissue Engineering Models of Inherited and Acquired Cardiomyopathies
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    Chapter 12 Badimon Perfusion Chamber: An Ex Vivo Model of Thrombosis
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    Chapter 13 Ischemic Model of Heart Failure in Rats and Mice
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    Chapter 14 Conventional Method of Transverse Aortic Constriction in Mice
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    Chapter 15 Characterization of the Differential Progression of Left Ventricular Remodeling in a Rat Model of Pressure Overload Induced Heart Failure. Does Clip Size Matter?
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    Chapter 16 Isoproterenol-Induced Heart Failure Mouse Model Using Osmotic Pump Implantation
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    Chapter 17 Rat Model of Cardiotoxic Drug-Induced Cardiomyopathy
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    Chapter 18 Pulmonary Artery Hypertension Model in Rats by Monocrotaline Administration
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    Chapter 19 The Sugen 5416/Hypoxia Mouse Model of Pulmonary Arterial Hypertension
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    Chapter 20 Mouse Model of Wire Injury-Induced Vascular Remodeling
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    Chapter 21 The Mouse Aortocaval Fistula Model with Intraluminal Drug Delivery
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    Chapter 22 A Pig Model of Myocardial Infarction: Catheter-Based Approaches
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    Chapter 23 Ovine Model of Ischemic Mitral Regurgitation
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    Chapter 24 Canine Model of Pacing-Induced Heart Failure
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    Chapter 25 Swine Model of Mitral Regurgitation Induced Heart Failure
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    Chapter 26 Pig Model of Increased Cardiac Afterload Induced by Ascending Aortic Banding
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    Chapter 27 Large Porcine Model of Profound Acute Ischemic Cardiogenic Shock
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    Chapter 28 Chronic Pulmonary Artery Embolization Models in Large Animals
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    Chapter 29 Modeling Pulmonary Hypertension: A Pig Model of Postcapillary Pulmonary Hypertension
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    Chapter 30 Development and Multiparametric Evaluation of Experimental Atherosclerosis in Rabbits
Attention for Chapter 7: Measuring Cardiomyocyte Contractility and Calcium Handling In Vitro
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Chapter title
Measuring Cardiomyocyte Contractility and Calcium Handling In Vitro
Chapter number 7
Book title
Experimental Models of Cardiovascular Diseases
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8597-5_7
Pubmed ID
Book ISBNs
978-1-4939-8596-8, 978-1-4939-8597-5
Authors

Przemek A. Gorski, Changwon Kho, Jae Gyun Oh, Gorski, Przemek A., Kho, Changwon, Oh, Jae Gyun

Abstract

In vitro measurements of cardiomyocyte contractility and Ca2+ handling have been used as a platform for determining physiological consequence of various genetic manipulations and identifying potential therapeutic targets for the treatment of heart failure. The Myocyte Calcium and Contractility System (IonOptix) offers a simultaneous trace of sarcomere movements and changes of intracellular Ca2+ levels in a single cardiomyocyte. Herein, we describe a modified protocol for the isolation of adult cardiomyocytes from murine hearts and provide a step-by-step description on how to analyze cardiomyocyte Ca2+ transient and contractility data collected using the IonOptix system. In our modified protocol, we recommend a novel cannulation technique which simplifies this difficult method and leads to improved viability of isolated cardiomyocytes. In addition, a comprehensive analysis of intracellular Ca2+ handling, SR Ca2+ load, myofilament Ca2+ sensitivity, and cardiomyocyte contractility is described in order to provide important insights into myocardial mechanics.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 40 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 13%
Student > Bachelor 4 10%
Researcher 4 10%
Student > Master 4 10%
Student > Doctoral Student 3 8%
Other 4 10%
Unknown 16 40%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 12 30%
Medicine and Dentistry 5 13%
Engineering 4 10%
Pharmacology, Toxicology and Pharmaceutical Science 2 5%
Immunology and Microbiology 1 3%
Other 1 3%
Unknown 15 38%