The role of sirtuins in the regulation of metabolic homeostasis in skeletal muscleRyall, James G.Current Opinion in Clinical Nutrition & Metabolic Care: November 2012 - Volume 15 - Issue 6 - p 561–566 doi: 10.1097/MCO.0b013e3283590914 NUTRITION AND PHYSIOLOGICAL FUNCTION: Edited by Annemie Schols and Labros S Sidossis Abstract Author Information Abstract Purpose of review: To discuss recent findings regarding the role of the histone deacetylase sirtuin SirT1 in anabolic and catabolic signaling pathways in skeletal muscle. Recent findings: Since its discovery as a regulator of peroxisome proliferator-activated receptor γ-coactivator 1α transcriptional activity, SirT1 has received much attention for its role in the regulation of tissue-specific and whole body regulation of metabolic processes. Although these early seminal discoveries identified SirT1 as a central player in metabolism, it is only more recently that we have begun to understand the complexities of SirT1 signaling. In addition to peroxisome proliferator-activated receptorgamma-coactivator 1α, SirT1 has been found to regulate the activity and/or transcription of protein kinase B, mammalian target of rapamycin, forkhead box O 1 and 3a and myogenic determination factor, all of which are central players in the regulation of energy status in skeletal muscle, via actions on catabolic and anabolic signaling. Summary: SirT1-mediated regulation of skeletal muscle metabolism (and indeed, whole body metabolism) likely occurs at numerous levels, from cell membrane receptors to transcription factors and histones. The end result of these regulatory actions of SirT1 is to maintain cellular homeostasis. Author Information National Institute of Arthritis, and Musculoskeletal and Skin diseases, National Institutes of Health (NIH), Bethesda, Maryland, USA Correspondence to James G. Ryall, PhD, National Institute of Arthritis, and Musculoskeletal and Skin diseases, National Institutes of Health (NIH), Bethesda, MD 20892, USA. Tel: +1 301 402 5072; e-mail: email@example.com © 2012 Lippincott Williams & Wilkins, Inc.