Zhang Han, Muhetarijiang Mairedan, Chen Ryan J, Hu Xiaosheng, Han Jie, Zheng Liangrong, Chen Ting
Department of Cardiology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
School of Medicine, Zhejiang University, Hangzhou, China.
Aging Dis. 2024 May 11. doi: 10.14336/AD.2024.0058.
Cardiovascular aging is a progressive remodeling process constituting a variety of cellular and molecular alterations that are closely linked to mitochondrial dysfunction. Therefore, gaining a deeper understanding of the changes in mitochondrial function during cardiovascular aging is crucial for preventing cardiovascular diseases. Cardiac aging is accompanied by fibrosis, cardiomyocyte hypertrophy, metabolic changes, and infiltration of immune cells, collectively contributing to the overall remodeling of the heart. Similarly, during vascular aging, there is a profound remodeling of blood vessel structure. These remodeling present damage to endothelial cells, increased vascular stiffness, impaired formation of new blood vessels (angiogenesis), the development of arteriosclerosis, and chronic vascular inflammation. This review underscores the role of mitochondrial dysfunction in cardiac aging, exploring its impact on fibrosis and myocardial alterations, metabolic remodeling, immune response remodeling, as well as in vascular aging in the heart. Additionally, we emphasize the significance of mitochondria-targeted therapies in preventing cardiovascular diseases in the elderly.
心血管衰老为渐进性重塑过程,由多种与线粒体功能障碍密切相关的细胞和分子改变构成。因此,深入了解心血管衰老过程中线粒体功能的变化对于预防心血管疾病至关重要。心脏衰老伴有纤维化、心肌细胞肥大、代谢变化以及免疫细胞浸润,这些共同促成了心脏的整体重塑。同样,在血管衰老过程中,血管结构会发生显著重塑。这些重塑表现为对内皮细胞的损伤、血管僵硬度增加、新生血管形成(血管生成)受损、动脉粥样硬化的发展以及慢性血管炎症。本综述强调线粒体功能障碍在心脏衰老中的作用,探讨其对纤维化和心肌改变、代谢重塑、免疫反应重塑以及心脏血管衰老的影响。此外,我们强调了线粒体靶向治疗在预防老年人心血管疾病方面的重要性。