Evidence map›Paper›PMID 39909868›Full record

ArticleAnimal models and experimental medicine2025

Development of an atherosclerosis rabbit model to evaluate the hemodynamic impact of extracorporeal circulation.

Anna Kathrin Assmann, Jan Buschmann, Sinje Reimers, Aleyna Karakas, Elvira Weber, Hug Aubin, Artur Lichtenberg, Alexander Assmann

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Article in Animal models and experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Anna Kathrin AssmannDepartment of Cardiac Surgery and CURE 3D Lab, Medical Faculty, Heinrich Heine University, University Hospital Düsseldorf, Düsseldorf, Germany.ORCID 0000-0002-9025-8640
Jan BuschmannCURE 3D Lab, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Sinje ReimersDepartment of Cardiac Surgery and CURE 3D Lab, Medical Faculty, Heinrich Heine University, University Hospital Düsseldorf, Düsseldorf, Germany.
Aleyna KarakasCURE 3D Lab, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Elvira WeberCURE 3D Lab, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Hug AubinDepartment of Cardiac Surgery and CURE 3D Lab, Medical Faculty, Heinrich Heine University, University Hospital Düsseldorf, Düsseldorf, Germany.
Artur LichtenbergDepartment of Cardiac Surgery and CURE 3D Lab, Medical Faculty, Heinrich Heine University, University Hospital Düsseldorf, Düsseldorf, Germany.
Alexander AssmannDepartment of Cardiac Surgery and CURE 3D Lab, Medical Faculty, Heinrich Heine University, University Hospital Düsseldorf, Düsseldorf, Germany.

Funding

German Heart Foundation/German Foundation of Heart Research
6 · The paper itself

Abstract

backgroundAortic atherosclerosis increases the risk of embolic events under extracorporeal circulation (ECC). To evaluate the hemodynamic impact of ECC on atheromatous plaques, an atherosclerosis animal model, which is also eligible for ECC, is required.

methodsTwenty-nine New Zealand White rabbits received a pro-atherosclerotic diet (group diet, n = 10), a pro-atherosclerotic diet and additional intraaortic balloon insufflation injury (group BI, n = 9), or served as controls (n = 10). After 3 or 6 months, aortic explants were analyzed by (immuno-)histology and RT-PCR.

resultsBlood serum analyses revealed increased cholesterol-levels in groups diet and BI compared to controls (3 months: p = 0.03 each, 6 months: p < 0.0001 each). Aortic inflammatory infiltration was significantly enhanced in groups diet (CD3 at 3 months: p < 0.0001, 6 months: p = 0.02; CD68 at 3 months: p = 0.01) and BI (CD3 at 3 months: p < 0.0001, 6 months: p = 0.03; CD68 at 3 months: p = 0.04, 6 months: p = 0.02). Increased intima hyperplasia occurred in both groups (p < 0.0001 each). Macroscopic analyses after 3 and 6 months showed ubiquitous lumen-narrowing aortic plaques. Calcification of the intima and media was increased in groups diet (intima: p < 0.0001 at 3 and 6 months; media at 3 months: p < 0.0001, 6 months: p = 0.01) and BI (intima: p < 0.0001 at 3 and 6 months; media at 3 months: p < 0.0001, 6 months: p = 0.02). Extensive lipid accumulation was found in the intima in both treatment groups (p < 0.0001 each).

conclusionsA rabbit model with high aortic calcific plaque burden-diet-induced with no implicit need of an additional intimal injury by an intraaortic balloon insufflation due to comparable outcome-exhibiting multiple pathophysiological aspects of human atherosclerosis has been designed and thoroughly characterized. It is suitable for use in future studies on the interaction between atherosclerotic plaques and the arterial blood flow under ECC.

Indexed as

AtherosclerosisDisease Models, AnimalExtracorporeal CirculationHemodynamicsAnimalsAortaMalePlaque, AtheroscleroticRabbitsanimal modelatherosclerosiscalcificationextracorporeal circulationinflammationplaques

Identifiers

PMID39909868
PMCPMC11904102

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.