Sirt1 Regulates Aging and Resistance to Oxidative Stress in the Heart
Rutgers, The State University of New Jersey · Institute of Molecular Medicine · +1 more institution
Abstract
Silent information regulator (Sir)2, a class III histone deacetylase, mediates lifespan extension in model organisms and prevents apoptosis in mammalian cells. However, beneficial functions of Sir2 remain to be shown in mammals in vivo at the organ level, such as in the heart. We addressed this issue by using transgenic mice with heart-specific overexpression of Sirt1, a mammalian homolog of Sir2. Sirt1 was significantly upregulated (4- to 8-fold) in response to pressure overload and oxidative stress in nontransgenic adult mouse hearts. Low (2.5-fold) to moderate (7.5-fold) overexpression of Sirt1 in transgenic mouse hearts attenuated age-dependent increases in cardiac hypertrophy, apoptosis/fibrosis, cardiac…
Citation impact
- FWCI
- 27.30
- Percentile
- 100%
- References
- 54
Authors
10- RRRalph R. AlcendorCorresponding
Rutgers, The State University of New Jersey, Institute of Molecular Medicine, Rutgers New Jersey Medical School
- SGShumin Gao
Rutgers, The State University of New Jersey, Institute of Molecular Medicine, Rutgers New Jersey Medical School
- PZPeiyong Zhai
Rutgers, The State University of New Jersey, Institute of Molecular Medicine, Rutgers New Jersey Medical School
- DZDaniela Zablocki
Rutgers, The State University of New Jersey, Institute of Molecular Medicine, Rutgers New Jersey Medical School
- EHEric Holle
Rutgers, The State University of New Jersey, Institute of Molecular Medicine, Rutgers New Jersey Medical School
Topics & keywords
- Oxidative stress
- Endocrinology
- Internal medicine
- Senescence
- Biology
- Sirtuin 1
- Cardiomyopathy
- Downregulation and upregulation