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在7T场强下通过扩散张量磁共振成像评估肥胖相关心脏功能障碍小鼠模型的心肌微观结构

Assessment of Myocardial Microstructure in a Murine Model of Obesity-Related Cardiac Dysfunction by Diffusion Tensor Magnetic Resonance Imaging at 7T.

作者信息

Lohr David, Thiele Arne, Stahnke Max, Braun Vera, Smeir Elia, Spranger Joachim, Brachs Sebastian, Klopfleisch Robert, Foryst-Ludwig Anna, Schreiber Laura M, Kintscher Ulrich, Beyhoff Niklas

机构信息

Chair of Molecular and Cellular Imaging, Comprehensive Heart Failure Center (CHFC), University Hospital Wuerzburg, Wuerzburg, Germany.

Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute of Pharmacology, Cardiovascular-Metabolic-Renal Research Center, Berlin, Germany.

出版信息

Front Cardiovasc Med. 2022 Apr 5;9:839714. doi: 10.3389/fcvm.2022.839714. eCollection 2022.

Abstract

BACKGROUND

Obesity exerts multiple deleterious effects on the heart that may ultimately lead to cardiac failure. This study sought to characterize myocardial microstructure and function in an experimental model of obesity-related cardiac dysfunction.

METHODS

Male C57BL/6N mice were fed either a high-fat diet (HFD; 60 kcal% fat, = 12) or standard control diet (9 kcal% fat, = 10) for 15 weeks. At the end of the study period, cardiac function was assessed by ultra-high frequency echocardiography, and hearts were processed for further analyses. The three-dimensional myocardial microstructure was examined at a spatial resolution of 100 × 100 × 100 μm by diffusion tensor magnetic resonance imaging (DT-MRI) at 7T. Myocardial deformation, diffusion metrics and fiber tract geometry were analyzed with respect to the different myocardial layers (subendocardium/subepicardium) and segments (base/mid-cavity/apex). Results were correlated with blood sample analyses, histopathology, and gene expression data.

RESULTS

HFD feeding induced significantly increased body weight combined with a pronounced accumulation of visceral fat (body weight 42.3 ± 5.7 vs. 31.5 ± 2.2 g, body weight change 73.7 ± 14.8 vs. 31.1 ± 6.6%, both < 0.001). Obese mice showed signs of diastolic dysfunction, whereas left-ventricular ejection fraction and fractional shortening remained unchanged (E/e' 41.6 ± 16.6 vs. 24.8 ± 6.0, < 0.01; isovolumic relaxation time 19 ± 4 vs. 14 ± 4 ms, < 0.05). Additionally, global longitudinal strain was reduced in the HFD group (-15.1 ± 3.0 vs. -20.0 ± 4.6%, = 0.01), which was mainly driven by an impairment in basal segments. However, histopathology and gene expression analyses revealed no myocardial fibrosis or differences in cardiomyocyte morphology. Mean diffusivity and eigenvalues of the diffusion tensor were lower in the basal subepicardium of obese mice as assessed by DT-MRI ( < 0.05). The three-dimensional fiber tract arrangement of the left ventricle (LV) remained preserved.

CONCLUSION

Fifteen weeks of high-fat diet induced alterations in myocardial diffusion properties in mice, whereas no remodeling of the three-dimensional myofiber arrangement of the LV was observed. Obese mice showed reduced longitudinal strain and lower mean diffusivity predominantly in the left-ventricular base, and further investigation into the significance of this regional pattern is required.

摘要

背景

肥胖对心脏产生多种有害影响,最终可能导致心力衰竭。本研究旨在描述肥胖相关心脏功能障碍实验模型中的心肌微观结构和功能。

方法

雄性C57BL/6N小鼠分别喂食高脂饮食(HFD;脂肪含量60千卡%,n = 12)或标准对照饮食(脂肪含量9千卡%,n = 10)15周。在研究期结束时,通过超高频率超声心动图评估心脏功能,并对心脏进行进一步分析。通过7T的扩散张量磁共振成像(DT-MRI)以100×100×100μm的空间分辨率检查三维心肌微观结构。针对不同心肌层(心内膜下/心外膜下)和节段(基部/腔中部/心尖)分析心肌变形、扩散指标和纤维束几何结构。结果与血样分析、组织病理学和基因表达数据相关联。

结果

喂食HFD导致体重显著增加,并伴有内脏脂肪的明显堆积(体重42.3±5.7 vs. 31.5±2.2克,体重变化73.7±14.8 vs. 31.1±6.6%,均P < 0.001)。肥胖小鼠表现出舒张功能障碍的迹象,而左心室射血分数和缩短分数保持不变(E/e' 41.6±16.6 vs. 24.8±6.0,P < 0.01;等容舒张时间19±4 vs. 14±4毫秒,P < 0.05)。此外,HFD组的整体纵向应变降低(-15.1±3.0 vs. -20.0±4.6%,P = 0.01),这主要是由基部节段的损伤所致。然而,组织病理学和基因表达分析未发现心肌纤维化或心肌细胞形态学差异。通过DT-MRI评估,肥胖小鼠的心外膜下基部的平均扩散率和扩散张量特征值较低(P < 0.05)。左心室(LV)的三维纤维束排列保持完整。

结论

15周的高脂饮食诱导小鼠心肌扩散特性发生改变,而未观察到LV三维肌纤维排列的重塑。肥胖小鼠主要在左心室基部表现出纵向应变降低和平均扩散率降低,需要进一步研究这种区域模式的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d71/9016133/6c050d033bba/fcvm-09-839714-g001.jpg

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