Cardiovascular diseases have become one of the important factors that endanger human health, and post-translational modifications of related proteins play an important role in this. [1][2][3][4][5] Among them, acetylation and deacetylation have increasingly become the focus of research. The seven-member sirtuins family (SIRT1-7) belongs to the third deacetylase. In order to catalyse the deacetylation reaction, this protein requires the presence of nicotinamide adenine dinucleotide (NAD + ) to have deacetylation activity. Sirtuins are involved in a variety of physiological and pathological activities in the human body, including ageing, energy responses to low calorie availability and stress resistance, apoptosis, inflammation, regulate mitochondrial biogenesis and biological rhythm. We currently know the substrates of the sirtuins family proteins including p53, 6 nuclear factor-kappa B (NF-κB), 7 forkhead box protein O1 (FOXO1), 8 forkhead box