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bioRxiv · 10.1101/2023.01.25.525524

SIRT2 inhibition protects against cardiac hypertrophy and heart failure

Yang, X.·Chang, H.-C.·Tatekoshi, Y.·Balibegloo, M.·Wu, R.·Chen, C.·Sato, T.·Shapiro, J. S.·Ardehali, H.
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Abstract

Sirtuins (SIRT) exhibit deacetylation or ADP-ribosyltransferase activity and regulate a wide range of cellular processes in the nucleus, mitochondria and cytoplasm. The role of the only sirtuin that resides in the cytoplasm, SIRT2, in the development of heart failure (HF) and cardiac hypertrophy is not known. In this paper, we show that the hearts of mice with deletion of Sirt2 (Sirt2-/-) display improved cardiac function after ischemia-reperfusion (I/R) and pressure overload (PO), suggesting that SIRT2 exerts maladaptive effects in the heart in response to stress. Similar results were obtained in mice with cardiomyocyte-specific Sirt2 deletion. Mechanistic studies suggest that SIRT2 modulates cellular levels and activity of nuclear factor (erythroid-derived 2)-like 2 (NRF2), which results in reduced expression of antioxidant proteins. Deletion of Nrf2 in the hearts of Sirt2-/- mice reversed protection after PO. Finally, treatment of mouse hearts with a specific SIRT2 inhibitors reduces cardiac size and attenuates cardiac hypertrophy in response to PO. These data indicate that SIRT2 has detrimental effects in the heart and plays a role in the progression of HF and cardiac hypertrophy, which makes this protein a unique member of the SIRT family. Additionally, our studies provide a novel approach for treatment of cardiac hypertrophy by targeting SIRT2 pharmacologically, providing a novel avenue for the treatment of this disorder.

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Yang, X., Chang, H.-C., Tatekoshi, Y., Balibegloo, M., Wu, R., Chen, C., Sato, T., Shapiro, J. S., Ardehali, H.. 2023-01-25. SIRT2 inhibition protects against cardiac hypertrophy and heart failure. https://doi.org/10.1101/2023.01.25.525524

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