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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 24: Canine Model of Pacing-Induced Heart Failure
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Chapter title
Canine Model of Pacing-Induced Heart Failure
Chapter number 24
Book title
Experimental Models of Cardiovascular Diseases
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8597-5_24
Pubmed ID
Book ISBNs
978-1-4939-8596-8, 978-1-4939-8597-5
Authors

Jeffery C. Powers, Fabio Recchia, Powers, Jeffery C., Recchia, Fabio

Abstract

Tachypacing-induced heart failure is a well-established large animal model that recapitulates numerous pathophysiological, structural and molecular features of dilated cardiomyopathy and, more in general, of end-stage congestive heart failure. The left or the right ventricle is instrumented with pacing electrodes to impose supernormal heart rates, usually three times higher than baseline values, for a length of time that typically ranges between 3 and 5 weeks. The animal of choice is the dog, although this protocol has been successfully implemented also in pigs, sheep, and rabbits. This chapter provides detailed methodology and description of the dog model utilized in our laboratory, which is one of the variants described in literature. Chronic instrumentation is completed by adding probes and catheters necessary to obtain measures of cardiac function and hemodynamics and to withdraw blood samples from various vascular districts. The progression from compensated to decompensated heart failure is highly reproducible, therefore, due also to the phylogenetic proximity of dogs to humans, tachypacing-induced heart failure is considered a highly clinically relevant model for testing the efficacy of novel pharmacological and nonpharmacological therapeutic agents. This model typically produces heart failure as defined by an LV dP/dt max <1500 mmHg/s, end-diastolic pressure >25 mmHg, mean arterial pressure <85 mmHg, and an ejection fraction <35%. One can expect a mortality rate of 5-10% due to fatal arrhythmias.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 5 33%
Student > Doctoral Student 3 20%
Student > Ph. D. Student 2 13%
Other 1 7%
Researcher 1 7%
Other 0 0%
Unknown 3 20%
Readers by discipline Count As %
Medicine and Dentistry 6 40%
Veterinary Science and Veterinary Medicine 2 13%
Agricultural and Biological Sciences 1 7%
Chemistry 1 7%
Materials Science 1 7%
Other 1 7%
Unknown 3 20%