The George Washington School of Medicine, , Washington, District of Columbia, USA.
Heart. 2014 Apr;100(8):611-8. doi: 10.1136/heartjnl-2013-304657. Epub 2014 Jan 21.
The global epidemic of cardiovascular disease remains the leading cause of death in the USA and across the world. Functional and structural integrity of mitochondria are essential for the physiological function of the cardiovascular system. The metabolic adaptation observed in normal heart is lost in the failing myocardium, which becomes progressively energy depleted leading to impaired myocardial contraction and relaxation. Uncoupling of electron transfer from ATP synthesis leads to excess generation of reactive species, leading to widespread cellular injury and cardiovascular disease. Accumulation of mitochondrial DNA mutation has been linked to ischaemic heart disease, cardiomyopathy and atherosclerotic vascular disease. Mitochondria are known to regulate apoptotic and autophagic pathways that have been shown to play an important role in the development of cardiomyopathy and atherosclerosis. A number of pharmacological and non-pharmacological treatment options have been explored in the management of mitochondrial diseases with variable success.
全球心血管疾病的流行仍然是美国和世界各地的主要死亡原因。线粒体的功能和结构完整性对于心血管系统的生理功能至关重要。在衰竭的心肌中,正常心脏观察到的代谢适应丧失,导致心肌收缩和松弛受损,能量逐渐耗尽。电子传递与 ATP 合成的解偶联导致活性物质的过度产生,导致广泛的细胞损伤和心血管疾病。线粒体 DNA 突变的积累与缺血性心脏病、心肌病和动脉粥样硬化性血管疾病有关。已知线粒体调节凋亡和自噬途径,这些途径在心肌病和动脉粥样硬化的发展中起着重要作用。已经探索了许多药理学和非药理学的治疗选择来治疗线粒体疾病,但效果各不相同。