Cardiomyocyte myofilament function in common animal models of heart failure with preserved ejection fraction

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of molecular and cellular cardiology Pub Date : 2024-10-18 DOI:10.1016/j.yjmcc.2024.10.005
Vivek P. Jani , Navid Koleini , Axel J. Fenwick , Thomas E. Sharp , Traci T. Goodchild , Joseph A. Hill , David J. Lefer , Anthony Cammarato , David A. Kass
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Abstract

Human cardiomyocytes from very obese patients with heart failure and preserved ejection fraction (HFpEF) have markedly depressed calcium-activated tension and increased resting stiffness. To test if either are recapitulated by obese-HFpEF animal models, tension‑calcium and tension-sarcomere length relations were measured in myocytes from mice on a high fat diet (HFD) with L-NAME, ZSF1 rats, and Göttingen minipigs on HFD + DOCA (MP). Only MP myocytes displayed reduced Ca2+-activated tension, and none exhibited increased resting stiffness versus respective controls. Consistent with prior myofibrillar data, crossbridge attachment and detachment rates at matched tension were slower in rodent models, and detachment slower in MP.

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射血分数保留型心力衰竭常见动物模型的心肌细胞肌丝功能。
患有心力衰竭和射血分数保留(HFpEF)的极度肥胖患者的人类心肌细胞具有明显的钙激活张力降低和静息僵硬度增加的特点。为了测试肥胖-HFpEF 动物模型是否再现了这两种情况,我们测量了高脂饮食(HFD)加 L-NAME、ZSF1 大鼠和高脂饮食 + DOCA(MP)的哥廷根小型猪心肌细胞的张力-钙和张力-肌丝长度关系。与各自的对照组相比,只有 MP 心肌细胞显示出 Ca2+ 激活张力降低,而静息僵硬度均未增加。与之前的肌纤维数据一致,在啮齿类动物模型中,匹配张力下的交桥附着和脱落速度较慢,而在 MP 中,脱落速度较慢。
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来源期刊
CiteScore
10.70
自引率
0.00%
发文量
171
审稿时长
42 days
期刊介绍: The Journal of Molecular and Cellular Cardiology publishes work advancing knowledge of the mechanisms responsible for both normal and diseased cardiovascular function. To this end papers are published in all relevant areas. These include (but are not limited to): structural biology; genetics; proteomics; morphology; stem cells; molecular biology; metabolism; biophysics; bioengineering; computational modeling and systems analysis; electrophysiology; pharmacology and physiology. Papers are encouraged with both basic and translational approaches. The journal is directed not only to basic scientists but also to clinical cardiologists who wish to follow the rapidly advancing frontiers of basic knowledge of the heart and circulation.
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Editorial Board PERM1 regulates mitochondrial energetics through O-GlcNAcylation in the heart Corrigendum to "PGE2 protects against heart failure through inhibiting TGF-β1 synthesis in cardiomyocytes and crosstalk between TGF-β1 and GRK2" [Journal of Molecular and Cellular Cardiology. 172(2022) 63-77]. Retraction notice to “The novel antibody fusion protein rhNRG1-HER3i promotes heart regeneration by enhancing NRG1-ERBB4 signaling pathway” [Journal of Molecular and Cellular Cardiology 187 (2023) 26–37] Exercise training attenuates cardiac dysfunction induced by excessive sympathetic activation through an AMPK-KLF4-FMO2 axis
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