# In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models

**Authors:** Giovanni Risato, Raquel Brañas Casas, Marco Cason, Maria Bueno Marinas, Serena Pinci, Monica De Gaspari, Silvia Visentin, Stefania Rizzo, Gaetano Thiene, Cristina Basso, Kalliopi Pilichou, Natascia Tiso, Rudy Celeghin

PMC · DOI: 10.3390/cells13151264 · Cells · 2024-07-27

## TL;DR

This paper discusses how animal models like mice and zebrafish help researchers understand arrhythmogenic cardiomyopathy and develop better treatments.

## Contribution

The paper highlights the complementary roles of mice and zebrafish models in studying AC and advancing therapeutic strategies.

## Key findings

- Mice models provide insights into gene involvement and disease progression in AC.
- Zebrafish offer economic and genetic advantages for AC research despite phylogenetic differences.
- Combining animal and in vitro models enhances understanding of AC for improved treatments.

## Abstract

Arrhythmogenic cardiomyopathy (AC) is a hereditary cardiac disorder characterized by the gradual replacement of cardiomyocytes with fibrous and adipose tissue, leading to ventricular wall thinning, chamber dilation, arrhythmias, and sudden cardiac death. Despite advances in treatment, disease management remains challenging. Animal models, particularly mice and zebrafish, have become invaluable tools for understanding AC’s pathophysiology and testing potential therapies. Mice models, although useful for scientific research, cannot fully replicate the complexity of the human AC. However, they have provided valuable insights into gene involvement, signalling pathways, and disease progression. Zebrafish offer a promising alternative to mammalian models, despite the phylogenetic distance, due to their economic and genetic advantages. By combining animal models with in vitro studies, researchers can comprehensively understand AC, paving the way for more effective treatments and interventions for patients and improving their quality of life and prognosis.

## Linked entities

- **Species:** Mus musculus (taxon 10090), Danio rerio (taxon 7955)

## Full-text entities

- **Diseases:** arrhythmias (MESH:D001145), chamber dilation (MESH:D002311), AC (MESH:D019571), hereditary cardiac disorder (MESH:D009386), sudden cardiac death (MESH:D016757)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11311808/full.md

## References

287 references — full list in the complete paper: https://tomesphere.com/paper/PMC11311808/full.md

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Source: https://tomesphere.com/paper/PMC11311808