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. 2020 May 31;12(6):1616. doi: 10.3390/nu12061616

Table 2.

The roles of sirtuins in heart failure development acquired from experiments on knock-out and transgenic mice (adapted from Pillai et al., [84]).

SIRT1 Heart cell growth and development, mediation of cardiac hypertrophy, protection from ischemic injury; partial deficiency protects from pressure overload-induced hypertrophy and failure
SIRT2 Mediating ischemic injury due to attenuated programmed apoptosis
SIRT3 Protection from age-induced hypertrophy, fibrosis and contractile dysfunction, prevents susceptibility to cardiac hypertrophic stimuli
SIRT6 Protection from cardiac hypertrophy and heart failure
SIRT7 Protection from spontaneous cardiac hypertrophy and inflammatory cardiomyopathy
SIRT1 Low to moderate overexpression attenuates age-dependent decline in cardiac functions in mice, while high overexpression induces cardiac hypertrophy and heart failure
SIRT3 Cardiac-specific overexpression protects the heart from hypertrophic stimuli by preserving mitochondrial function
SIRT6 Cardiac-specific overexpression protects the heart from hypertrophic stimuli by blocking activation of Akt signaling at the level of chromatin