Bacova Barbara Szeiffova, Andelova Katarina, Sykora Matus, Egan Benova Tamara, Barancik Miroslav, Kurahara Lin Hai, Tribulova Narcis
Centre of Experimental Medicine, Slovak Academy of Sciences, 84104 Bratislava, Slovakia.
Department of Cardiovascular Physiology, Faculty of Medicine, Kagawa University, Miki-cho 761-0793, Japan.
Biomedicines. 2022 Nov 4;10(11):2819. doi: 10.3390/biomedicines10112819.
This review focuses on cardiac atrophy resulting from mechanical or metabolic unloading due to various conditions, describing some mechanisms and discussing possible strategies or interventions to prevent, attenuate or reverse myocardial atrophy. An improved awareness of these conditions and an increased focus on the identification of mechanisms and therapeutic targets may facilitate the development of the effective treatment or reversion for cardiac atrophy. It appears that a decrement in the left ventricular mass itself may be the central component in cardiac deconditioning, which avoids the occurrence of life-threatening arrhythmias. The depressed myocardial contractility of atrophied myocardium along with the upregulation of electrical coupling protein, connexin43, the maintenance of its topology, and enhanced PKCƐ signalling may be involved in the anti-arrhythmic phenotype. Meanwhile, persistent myocardial atrophy accompanied by oxidative stress and inflammation, as well as extracellular matrix fibrosis, may lead to severe cardiac dysfunction, and heart failure. Data in the literature suggest that the prevention of heart failure via the attenuation or reversion of myocardial atrophy is possible, although this requires further research.
本综述聚焦于因各种情况导致的机械性或代谢性负荷减轻所引起的心脏萎缩,描述了一些机制,并讨论了预防、减轻或逆转心肌萎缩的可能策略或干预措施。对这些情况的进一步认识以及对机制和治疗靶点识别的更多关注,可能有助于开发针对心脏萎缩的有效治疗或逆转方法。左心室质量本身的减少似乎可能是心脏功能失调的核心组成部分,这可避免危及生命的心律失常的发生。萎缩心肌的心肌收缩力降低,同时电偶联蛋白连接蛋白43上调、其拓扑结构得以维持以及蛋白激酶CƐ信号增强,这些可能与抗心律失常表型有关。与此同时,持续性心肌萎缩伴有氧化应激、炎症以及细胞外基质纤维化,可能导致严重的心功能障碍和心力衰竭。文献数据表明,通过减轻或逆转心肌萎缩来预防心力衰竭是有可能的,尽管这还需要进一步研究。