Tissue Preparation Techniques for Contrast-Enhanced Micro Computed Tomography Imaging of Large Mammalian Cardiac Models with Chronic Disease.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
08 02 2022
Historique:
entrez: 28 2 2022
pubmed: 1 3 2022
medline: 8 4 2022
Statut: epublish

Résumé

Structural remodeling is a common consequence of chronic pathological stresses imposed on the heart. Understanding the architectural and compositional properties of diseased tissue is critical to determine their interactions with arrhythmic behavior. Microscale tissue remodeling, below the clinical resolution, is emerging as an important source of lethal arrhythmia, with high prevalence in young adults. Challenges remain in obtaining high imaging contrast at sufficient microscale resolution for preclinical models, such as large mammalian whole hearts. Moreover, tissue composition-selective contrast enhancement for three-dimensional high-resolution imaging is still lacking. Non-destructive imaging using micro-computed tomography shows promise for high-resolution imaging. The objective was to alleviate sufferance from X-ray over attenuation in large biological samples. Hearts were extracted from healthy pigs (N = 2), and sheep (N = 2) with either induced chronic myocardial infarction and fibrotic scar formation or induced chronic atrial fibrillation. Excised hearts were perfused with: a saline solution supplemented with a calcium ion quenching agent and a vasodilator, ethanol in serial dehydration, and hexamethyldisilizane under vacuum. The latter reinforced the heart structure during air-drying for 1 week. Collagen-dominant tissue was selectively bound by an X-ray contrast-enhancing agent, phosphomolybdic acid. Tissue conformation was stable in air, permitting long-duration microcomputed tomography acquisitions to obtain high-resolution (isotropic 20.7 µm) images. Optimal contrast agent loading by diffusion showed selective contrast enhancement of the epithelial layer and sub-endocardial Purkinje fibers in healthy pig ventricles. Atrial fibrillation (AF) hearts showed enhanced contrast accumulation in the posterior walls and appendages of the atria, attributed to greater collagen content. Myocardial infarction hearts showed increased contrast selectively in regions of cardiac fibrosis, which enabled the identification of interweaving surviving myocardial muscle fibers. Contrast-enhanced air-dried tissue preparations enabled microscale imaging of the intact large mammalian heart and selective contrast enhancement of underlying disease constituents.

Identifiants

pubmed: 35225260
doi: 10.3791/62909
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Néstor Pallares-Lupon (N)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Jason D Bayer (JD)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Bastien Guillot (B)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Guido Caluori (G)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Girish S Ramlugun (GS)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Kanchan Kulkarni (K)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Virginie Loyer (V)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Stephane Bloquet (S)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Dounia El Hamrani (D)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Jérôme Naulin (J)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Marion Constantin (M)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Pierre Dos Santos (P)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.; Electrophysiology and Ablation Unit, Bordeaux University Hospital (CHU).

Olivier Bernus (O)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Pierre Jaïs (P)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.; Electrophysiology and Ablation Unit, Bordeaux University Hospital (CHU).

Philippe Pasdois (P)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.

Richard D Walton (RD)

Centre de recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux; IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Univ.; richard.walton@ihu-liryc.fr.

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Classifications MeSH