Menopause Review (Apr 2011)

SIRT1 and metabolic syndrome

  • Katarzyna Mac-Marcjanek,
  • Marzena Wojcik,
  • Katarzyna Cypryk

Journal volume & issue
Vol. 15, no. 2
pp. 139 – 146

Abstract

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Both obesity and type 2 diabetes mellitus, two major components of metabolic syndrome, become healthepidemics in the world. Over the past decade, advances in understanding the role of some regulators participatingin lipid and carbohydrate homeostasis have been made.Of them, SIRT1, the mammalian orthologue of the yeast Sir2 protein has been identified. SIRT1 is a nuclearNAD+-dependent deacetylase that targets many transcriptional modulators, including PPAR-α and -γ (peroxisomeproliferator-activated receptors α and γ), PGC-1α (PPAR-γ coactivator-1α), FOXO (forkhead box O proteins),and nuclear factor κB (NF-κB), thereby this enzyme mediates a wide range of physiological processes like apoptosis,fat metabolism, glucose homeostasis, and neurodegeneration.In this article, we discuss how SIRT1 regulates lipid and carbohydrate metabolism, and insulin secretion indifferent metabolic organs/tissue, including liver, muscle, pancreas, and fat. Additionally, the role of this enzymein reduction of inflammatory signalling is highlighted.

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