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Calorie restriction can reverse, as well as prevent, aging cardiomyopathy
Lin Yan1, Shumin Gao, David Ho
1Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, UMDNJ-New Jersey Medical School, 185 South Orange Avenue, MSB G-609, Newark, NJ, 07103, USA, yanl2@umdnj.edu.
Calorie restriction (CR) can reverse aging cardiomyopathy in mice, even when started later in life. This intervention fully restored heart function and structure, offering potential therapeutic benefits for age-related heart disease.
Area of Science:
- Cardiology
- Gerontology
- Molecular Biology
Background:
- Calorie restriction (CR) is a well-researched intervention for mitigating aging effects.
- Previous studies on CR and aging cardiomyopathy focused on early intervention, yielding only partial prevention.
- Aging cardiomyopathy is characterized by impaired cardiac function, hypertrophy, apoptosis, and fibrosis.
Purpose of the Study:
- To investigate if CR, initiated after the onset of aging cardiomyopathy, could reverse the condition.
- To determine the therapeutic potential of late-life CR in correcting age-related cardiac dysfunction.
Main Methods:
- Aging cardiomyopathy was induced in 20-month-old mice.
- Short-term (2 months) CR was administered to mice with established aging cardiomyopathy.
- Cardiac function, left ventricular (LV) weight, myocardial fibrosis, apoptosis, and cytoskeletal protein alterations were assessed.
Main Results:
- CR initiated in older mice rapidly reversed cardiac dysfunction and structural changes associated with aging cardiomyopathy.
- Post-CR hearts were indistinguishable from young controls or those treated with CR from a young age.
- While apoptosis did not revert to normal, CR corrected cytoskeletal protein alterations linked to cardiomyopathy.
Conclusions:
- This study demonstrates complete reversal of aging cardiomyopathy by CR, even when initiated later in life.
- Late-life CR offers a rapid and effective therapeutic strategy for age-related cardiac conditions.
- The findings suggest CR's benefits may stem from correcting cytoskeletal abnormalities rather than solely reducing apoptosis.
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