As average lifespan of humans increases in western countries, cardiac diseases become the first cause of death. Aging is among the most important risk factors that increase susceptibility for developing cardiovascular diseases. The heart has very aerobic metabolism, and is highly dependent on mitochondrial function, since mitochondria generate more than 90 % of the intracellular ATP consumed by cardiomyocytes. In the last few decades, several investigations have supported the relevance of mitochondria and oxidative stress both in heart aging and in the development of cardiac diseases such as heart failure, cardiac hypertrophy, and diabetic cardiomyopathy. In the current review, we compile different studies corroborating this role. Increased mitochondria DNA instability, impaired bioenergetic efficiency, enhanced apoptosis, and inflammation processes are some of the events related to mitochondria that occur in aging heart, leading to reduced cellular survival and cardiac dysfunction. Knowing the mitochondrial mechanisms involved in the aging process will provide a better understanding of them and allow finding approaches to more efficiently improve this process.
Keyphrases
- oxidative stress
- heart failure
- cell death
- reactive oxygen species
- left ventricular
- endoplasmic reticulum
- risk factors
- atrial fibrillation
- diabetic rats
- dna damage
- ischemia reperfusion injury
- induced apoptosis
- cardiovascular disease
- type diabetes
- endoplasmic reticulum stress
- cell proliferation
- signaling pathway
- south africa
- metabolic syndrome
- endothelial cells
- cell cycle arrest
- high intensity
- wound healing
- heat stress
- free survival