AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity

摘要

AMP-activated protein kinase (AMPK) is a metabolic fuel gauge conserved along the evolutionary scale in eukaryotes that senses changes in the intracellular AMP/ATP ratio. The interest in AMPK has recently been raised by evidence showing that AMPK plays an important role to explain the therapeutic benefits of metformin^, , thiazolidinediones and exercise, which form the cornerstones of the clinical management of type 2 diabetes and associated metabolic disorders. In general, activation of AMPK acts to maintain cellular energy stores, switching on catabolic pathways that produce ATP, mostly by enhancing oxidative metabolism and mitochondrial biogenesis, while switching off anabolic pathways that consume ATP. This regulation can take place acutely, through the regulation of fast post-translational events, but also by transcriptionally reprogramming the cell in order to meet energetic needs. Our study demonstrates that AMPK controls the expression of genes involved in energy metabolism in skeletal muscle by acting in coordination with another metabolic sensor, the NAD⁺-dependent type III deacetylase SIRT1. AMPK enhances SIRT1 activity by increasing cellular NAD⁺ levels, resulting in the deacetylation and modulation of the activity of downstream SIRT1 targets that include the peroxisome proliferator-activated receptor-γ coactivator 1α and the forkhead transcription factors FOXO1 and FOXO3a. The AMPK-induced SIRT1-mediated deacetylation of these targets explains many of the convergent biological effects of AMPK and SIRT1 on energy metabolism.