# Animal Models of Restenosis and Intimal Hyperplasia in Cardiovascular Percutaneous Interventions: A Narrative Review

**Authors:** Sabrina Houthoofd, Marc Vuylsteke, Serge Mordon, Inge Fourneau

PMC · DOI: 10.3390/biomedicines14020309 · Biomedicines · 2026-01-29

## TL;DR

This review discusses animal models used to study restenosis and intimal hyperplasia after cardiovascular procedures, emphasizing the importance of model selection for effective research.

## Contribution

The paper provides a comprehensive overview of animal models for restenosis and highlights the importance of considering interspecies differences in translational research.

## Key findings

- A variety of animal models, including rodents, rabbits, and swine, are used to study restenosis and intimal hyperplasia.
- Interspecies differences significantly affect vascular healing responses and translational relevance.
- Careful model selection is critical for improving translational outcomes and clinical applications.

## Abstract

Background: Restenosis and intimal hyperplasia following arterial bypass surgery or percutaneous interventions remain major clinical challenges that significantly impair long-term vessel patency and clinical outcomes, despite substantial technological progress. Preclinical research aimed at understanding the biological mechanisms underlying restenosis and developing effective therapeutic strategies relies heavily on experimental animal models. Methods: A narrative review of the literature was conducted using PubMed, Embase, Web of Science Core Collection, and the Cochrane Library to identify relevant studies describing animal models of restenosis and intimal hyperplasia following percutaneous cardiovascular interventions. Results: The reviewed studies describe a broad range of animal models, including rodents, rabbits, swine, and other large animals, with each species exhibiting distinct anatomical, physiological, and pathological characteristics that influence its suitability for studying restenosis and intimal hyperplasia. Considerable interspecies variability exists in vascular healing responses, inflammatory processes, and translational relevance. Conclusions: Animal models remain indispensable tools for investigating restenosis and intimal hyperplasia and for evaluating novel pharmacological and device-based therapies. Understanding interspecies differences is essential for designing appropriate experimental studies and interpreting findings. Careful animal model selection is critical to improving translational relevance and facilitating successful clinical translation.

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}
- **Diseases:** coronary and peripheral arterial disease (MESH:D058729), hypercholesterolemia (MESH:D006937), obese (MESH:D009765), atheromas (MESH:D058226), Hyperplasia (MESH:D006965), necrosis (MESH:D009336), hypertensive (MESH:D006973), dyslipidemia (MESH:D050171), atherosclerosis (MESH:D050197), injury to (MESH:D014947), inflammation (MESH:D007249), Restenosis (MESH:D023903), hyperlipidemia (MESH:D006949), fibrosis (MESH:D005355), thrombosis (MESH:D013927), vascular injury (MESH:D057772), cardiovascular disease (MESH:D002318), diabetes (MESH:D003920), endothelial dysfunction (MESH:D014652), calcification (MESH:D002114)
- **Chemicals:** lipids (MESH:D008055), cholesterol (MESH:D002784)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Sus scrofa (pig, species) [taxon 9823], Canis lupus familiaris (dog, subspecies) [taxon 9615], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937994/full.md

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Source: https://tomesphere.com/paper/PMC12937994