Probing Early Myocardial Remodeling in Response to a High-Fat Diet in Mice by Evaluation of Extracellular Volume Fraction Using 4D Retrospectively Gated Micro-CT Imaging.

IF 2.5 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Grzegorz Kwiatkowski, Anna Gąsiorek, Izabela Ciastoń, Joanna Kozieł, Greetje Vande Velde, Stefan Chłopicki
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Abstract

Purpose: The objective of this study was to evaluate whether retrospectively gated 4D micro-computed tomography (µCT) can quantify extracellular volume fraction (ECV) as an early marker of myocardial fibrosis and remodeling in a high-fat diet (HFD) mouse model, and to determine its relationship with cardiac functional parameters.

Procedures: Male C57BL/6J mice were assigned to control diet or high-fat diet (HFD) groups, with HFD animals imaged after 8 or 16 weeks of feeding and control animals scanned at an age-matched time point. Contrast-enhanced 4D µCT with ECG gating was performed for cardiac function analysis and pre/post-contrast imaging for ECV quantification, corrected for hematocrit. Functional measures included left ventricular (LV) volumes, ejection fraction, mitral annular plane systolic excursion (MAPSE), circumferential shortening, and dobutamine stress response.

Results: Global LV ECV significantly increased at 8 weeks of HFD compared to controls, preceding changes in LV mass and ejection fraction. Early ECV elevation correlated with impaired lateral MAPSE, indicating subtle functional impairment despite preserved global systolic function. At 16 weeks, further remodeling was evident with increased LV mass, reduced epicardial circumferential shortening, decreased left atrial ejection area, and diminished dobutamine-induced contractile reserve.

Conclusions: Retrospectively gated 4D µCT provides a robust and noninvasive method for early detection of diffuse myocardial fibrosis and functional impairment in small animal models. This approach enables longitudinal studies of cardiac disease progression and therapeutic interventions, offering translational value for preclinical cardiology research.

利用4D回顾性门控显微ct成像评价细胞外体积分数探讨小鼠对高脂肪饮食的早期心肌重构
目的:本研究的目的是评估回顾性门控4D微计算机断层扫描(µCT)是否可以量化细胞外体积分数(ECV)作为高脂肪饮食(HFD)小鼠模型中心肌纤维化和重构的早期标志物,并确定其与心功能参数的关系。实验过程:雄性C57BL/6J小鼠被分为控制饮食组和高脂肪饮食组(HFD), HFD动物在喂养8周或16周后成像,对照组动物在年龄匹配的时间点扫描。造影增强4D微CT伴ECG门控进行心功能分析,造影前/造影后进行ECV量化,校正红细胞压积。功能测量包括左心室(LV)容积、射血分数、二尖瓣环平面收缩偏移(MAPSE)、周向缩短和多巴酚丁胺应激反应。结果:与对照组相比,HFD 8周时整体左室ECV显著增加,之前左室质量和射血分数发生变化。早期ECV升高与侧位MAPSE受损相关,表明尽管保留了整体收缩功能,但存在细微的功能损伤。16周时,进一步的重构明显表现为左室体积增加,心外膜周缩短减少,左房射血面积减少,多巴酚丁胺诱导的收缩储备减少。结论:回顾性门控4DµCT为小动物模型弥漫性心肌纤维化和功能损害的早期检测提供了一种可靠且无创的方法。这种方法可以对心脏病进展和治疗干预进行纵向研究,为临床前心脏病学研究提供转化价值。
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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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