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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 9: Methods for the Preparation of an Excised, Cross-Circulated Rat Heart
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Chapter title
Methods for the Preparation of an Excised, Cross-Circulated Rat Heart
Chapter number 9
Book title
Experimental Models of Cardiovascular Diseases
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8597-5_9
Pubmed ID
Book ISBNs
978-1-4939-8596-8, 978-1-4939-8597-5
Authors

Koji Obata, Miyako Takaki, Obata, Koji, Takaki, Miyako

Abstract

The Emax-Pressure-Volume Area (PVA)-VO2 framework proposed by Dr. Suga for canine hearts has dramatically advanced the field of cardiac mechanical work and energetics, i.e., mechanoenergetics. He and his collaborators investigated mechanoenergetics in the left ventricle (LV) of excised, cross-circulated canine heart preparations. We instituted the excised cross-circulated rat whole heart preparations and found a curvilinear end-systolic pressure-volume relation (ESPVR) in the rat LV, in contrast to the linear ESPVR in canine, rabbit, and human LVs. Although Emax, the slope of the linear ESPVR, could be used as an index of LV contractility, it was not applicable for evaluating LV contractility in the rat LV. Thus, we proposed a new index of contractility, equivalent Emax (eEmax) in the rat LV. We also found a linear VO2-PVA relationship in the rat LV. Here, we introduce the methods for the preparation of excised, cross-circulated rat whole hearts and the eEmax-PVA-VO2 framework in the rat LV. Using this method, we can obtain accurate LV volume and myocardial O2 consumption in real time for estimating cardiac mechanoenergetics, which is very challenging in in vivo experiments.

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The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Lecturer 1 50%
Unknown 1 50%
Readers by discipline Count As %
Veterinary Science and Veterinary Medicine 1 50%
Unknown 1 50%