Canine Heart Validation

Canine heart validation is the systematic assessment of whether a canine heart model, tissue construct, imaging system, or bioengineered device accurately represents relevant cardiac structure and function. Validation compares model outputs with reference canine measurements, including anatomy, contractility, electrical activity, hemodynamics, and responses to defined loading or stimulation conditions. In bioengineering, this process helps determine whether an engineered heart platform can reliably reproduce clinically important behavior and support reproducible experiments. Rigorous validation strengthens preclinical evaluation of cardiovascular devices, therapies, and regenerative approaches while identifying model limitations before translation to human research.

Canine Heart Validation - Related Videos

Research

JoVE Journal - Medicine
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In Vivo Canine Muscle Function Assay

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Cited by 19 •

2011

We describe a minimally-invasive and painless method to measure canine hindlimb muscle strength and muscle response to repeated eccentric contractions.

Research

JoVE Journal - Bioengineering

Patient-specific Modeling of the Heart: Estimation of Ventricular Fiber Orientations

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Cited by 14 •

2013

A methodology to estimate ventricular fiber orientations from in vivo images of patient heart geometries for personalized modeling is described. Validation of the methodology performed using normal and failing canine hearts demonstrate that that there are no significant differences between estimated and acquired fiber orientations at a clinically observable level.

Isolation and Expansion of Adult Canine Hippocampal Neural Precursors

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Cited by 3 •

2016

The canine brain is a valuable model in which to study adult neurogenesis. Presented here are protocols for isolating and expanding adult canine hippocampal neural precursor cells from primary brain tissue.

Isolation and Culture of Primary Endothelial Cells from Canine Arteries and Veins

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Cited by 11 •

2016

Novel isolation methods of primary endothelial cells from blood vessels are needed. This protocol describes a new technique that completely inverts blood vessels of interest, exposing only the endothelial side to enzymatic digestion. The resulting pure endothelial cell culture can be used to study cardiovascular diseases, disease modelling, and angiogenesis.

A Simple Fluorescence Assay for Quantification of Canine Neutrophil Extracellular Trap Release

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Cited by 8 •

2016

Neutrophil extracellular traps (NETs) are networks of DNA, histones and neutrophil proteins. Although a component of the innate immune response, NETs are implicated in autoimmunity and thrombosis. This protocol describes a simple method for canine neutrophil isolation and quantification of NETs using a microplate fluorescence assay.

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