Longitudinal In Vivo Monitoring of Atheroprogression in Hypercholesterolemic Mice Using Photoacoustic Imaging

Author:

Ferraro Bartolo123,Giustetto Pierangela45,Schengel Olga6,Weckbach Ludwig T.2378,Maegdefessel Lars2910,Soehnlein Oliver12611

Affiliation:

1. Institute for Cardiovascular Prevention (IPEK), LMU Munich, Munich, Germany

2. DZHK, Partner Site Munich Heart Alliance, Munich, Germany

3. Institute of Cardiovascular Physiology and Pathophysiology, Biomedical Center, Ludwig- Maximilians-University Munich, Planegg-Martinsried, Germany

4. Fujifilm VisualSonics Consultant, Amsterdam, The Netherlands

5. Section of Physiology, Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy

6. Institute for Experimental Pathology (ExPat), Centre for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany

7. Medizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig-Maximilians-University Munich, Munich, Germany

8. Walter Brendel Centre of Experimental Medicine, Ludwig-Maximilians-University Munich, University Hospital, Planegg-Martinsried, Germany

9. Department of Vascular and Endovascular Surgery, Technical University Munich, Munich, Germany

10. Department of Medicine, Karolinska Institutet, Stockholm, Sweden

11. Department of Physiology and Pharmacology (FyFa), Karolinska Institutet, Stockholm, Sweden

Abstract

Background and Aim The ability to recognize and monitor atherosclerotic lesion development using noninvasive imaging is crucial in preventive cardiology. The aim of the present study was to establish a protocol for longitudinal monitoring of plaque lipid, collagen, and macrophage burden as well as of endothelial permeability. Methods and Results Photoacoustic signals derived from endogenous or exogenous dyes assessed in vivo, in plaques of albino Apoe −/− mice, correlated with lesion characteristics obtained after histomorphometric and immunofluorescence analyses, thus supporting the validity of our protocol. Using models of atheroprogression and regression, we could apply our imaging protocol to the longitudinal observation of atherosclerotic lesion characteristics in mice. Conclusions The present study shows an innovative approach to assess arterial inflammation in a non-invasive fashion, applicable to longitudinal analyses of changes of atherosclerotic lesion composition. Such approach could prove important in the preclinical testing of therapeutic interventions in mice carrying pre-established lesions.

Funder

Else Kröner Fresenius Stiftung

FUJIFILM Visualsonics, Inc.

Deutsche Forschungsgemeinschaft

Leducq Foundation

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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