Forever young: SIRT3 a shield against mitochondrial meltdown, aging, and neurodegeneration

Caloric restriction (CR), fasting, and exercise have long been recognized for their neuroprotective and lifespan-extending properties; however, the underlying mechanisms of these phenomena remain elusive. Such extraordinary benefits might be linked to the activation of sirtuins. In mammals, the sirtuin family has seven members (SIRT1–7), which diverge in tissue distribution, subcellular localization, enzymatic activity, and targets. SIRT1, SIRT2, and SIRT3 have deacetylase activity. Their dependence on NAD+ directly links their activity to the metabolic status of the cell. High NAD+ levels convey neuroprotective effects, possibly via activation of sirtuin family members. Mitochondrial sirtuin 3 (SIRT3) has received much attention for its role in metabolism and aging. Specific small nucleotide polymorphisms in Sirt3 are linked to increased human lifespan. SIRT3 mediates the adaptation of increased energy demand during CR, fasting, and exercise to increased production of energy equivalents. SIRT3 deacetylates and activates mitochondrial enzymes involved in fatty acid β-oxidation, amino acid metabolism, the electron transport chain, and antioxidant defenses. As a result, the mitochondrial energy metabolism increases. In addition, SIRT3 prevents apoptosis by lowering reactive oxygen species and inhibiting components of the mitochondrial permeability transition pore. Mitochondrial deficits associated with aging and neurodegeneration might therefore be slowed or even prevented by SIRT3 activation. In addition, upregulating SIRT3 activity by dietary supplementation of sirtuin activating compounds might promote the beneficial effects of this enzyme. The goal of this review is to summarize emerging data supporting a neuroprotective action of SIRT3 against Alzheimer’s disease, Huntington’s disease, Parkinson’s disease, and amyotrophic lateral sclerosis.

[1]  G. Shulman,et al.  AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Eric Verdin,et al.  Mitochondrial sirtuins: regulators of protein acylation and metabolism , 2012, Trends in Endocrinology & Metabolism.

[3]  C. Franceschi,et al.  A novel VNTR enhancer within the SIRT3 gene, a human homologue of SIR2, is associated with survival at oldest ages. , 2005, Genomics.

[4]  Gregory C Kujoth,et al.  Endurance exercise rescues progeroid aging and induces systemic mitochondrial rejuvenation in mtDNA mutator mice , 2011, Proceedings of the National Academy of Sciences.

[5]  E. Verdin,et al.  Mitochondrial acetylome analysis in a mouse model of alcohol-induced liver injury utilizing SIRT3 knockout mice. , 2012, Journal of proteome research.

[6]  J. Friedman,et al.  Reduced mitochondrial function in obesity-associated fatty liver: SIRT3 takes on the fat , 2011, Aging.

[7]  R. Patel,et al.  Interaction of Sirt3 with OGG1 contributes to repair of mitochondrial DNA and protects from apoptotic cell death under oxidative stress , 2013, Cell Death and Disease.

[8]  D. Reinberg,et al.  SirT3 is a nuclear NAD+-dependent histone deacetylase that translocates to the mitochondria upon cellular stress. , 2007, Genes & development.

[9]  A. Yashin,et al.  Variability of the SIRT3 gene, human silent information regulator Sir2 homologue, and survivorship in the elderly , 2003, Experimental Gerontology.

[10]  Robert V Farese,et al.  SIRT 3 Deficiency and Mitochondrial Protein Hyperacetylation Accelerate the Development of the Metabolic Syndrome , 2011 .

[11]  L. Sokoloff,et al.  Relationships among local functional activity, energy metabolism, and blood flow in the central nervous system. , 1981, Federation proceedings.

[12]  Robert V Farese,et al.  SIRT 3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation , 2010 .

[13]  C. Blackstone,et al.  Release of OPA1 during Apoptosis Participates in the Rapid and Complete Release of Cytochrome c and Subsequent Mitochondrial Fragmentation* , 2005, Journal of Biological Chemistry.

[14]  N. Grishin,et al.  Substrate and functional diversity of lysine acetylation revealed by a proteomics survey. , 2006, Molecular cell.

[15]  H. Pitot,et al.  Aging lowers steady-state antioxidant enzyme and stress protein expression in primary hepatocytes. , 2001, The journals of gerontology. Series A, Biological sciences and medical sciences.

[16]  Wei Yu,et al.  Sirt3 Mediates Reduction of Oxidative Damage and Prevention of Age-Related Hearing Loss under Caloric Restriction , 2010, Cell.

[17]  Kevin Y. Leea,et al.  Sirtuin-3 ( Sirt 3 ) regulates skeletal muscle metabolism and insulin signaling via altered mitochondrial oxidation and reactive oxygen species production , 2011 .

[18]  A. Verkhratsky,et al.  Changes in Mitochondrial Status Associated with Altered Ca2+ Homeostasis in Aged Cerebellar Granule Neurons in Brain Slices , 2002, The Journal of Neuroscience.

[19]  L. Laffel Ketone bodies: a review of physiology, pathophysiology and application of monitoring to diabetes , 1999, Diabetes/metabolism research and reviews.

[20]  Masaaki Komatsu,et al.  Loss of autophagy in the central nervous system causes neurodegeneration in mice , 2006, Nature.

[21]  A. Bonen,et al.  In mammalian muscle, SIRT3 is present in mitochondria and not in the nucleus; and SIRT3 is upregulated by chronic muscle contraction in an adenosine monophosphate-activated protein kinase-independent manner. , 2012, Metabolism: clinical and experimental.

[22]  Ian R. Lanza,et al.  Endurance Exercise as a Countermeasure for Aging , 2008, Diabetes.

[23]  C. Steegborn,et al.  Substrates and regulation mechanisms for the human mitochondrial sirtuins Sirt3 and Sirt5. , 2008, Journal of molecular biology.

[24]  D. Harman Aging: a theory based on free radical and radiation chemistry. , 1956, Journal of gerontology.

[25]  J. Tower,et al.  Induced overexpression of mitochondrial Mn-superoxide dismutase extends the life span of adult Drosophila melanogaster. , 2002, Genetics.

[26]  C. Pál,et al.  Natural selection promotes the conservation of linkage of co-expressed genes. , 2002, Trends in genetics : TIG.

[27]  C. Brocker,et al.  Non-P450 aldehyde oxidizing enzymes: the aldehyde dehydrogenase superfamily , 2008, Expert opinion on drug metabolism & toxicology.

[28]  Danica Chen,et al.  Calorie restriction reduces oxidative stress by SIRT3-mediated SOD2 activation. , 2010, Cell metabolism.

[29]  M. Mattson,et al.  Dietary restriction protects hippocampal neurons against the death-promoting action of a presenilin-1 mutation , 1999, Brain Research.

[30]  E. Bossy‐Wetzel,et al.  Mutant SOD1G93A triggers mitochondrial fragmentation in spinal cord motor neurons: Neuroprotection by SIRT3 and PGC-1α , 2013, Neurobiology of Disease.

[31]  L. Guarente,et al.  Genetic pathways that regulate ageing in model organisms , 2000, Nature.

[32]  J. D. Brown,et al.  AMP-activated protein kinase phosphorylates transcription factors of the CREB family. , 2008, Journal of applied physiology.

[33]  Enxuan Jing,et al.  Sirtuin-3 (Sirt3) regulates skeletal muscle metabolism and insulin signaling via altered mitochondrial oxidation and reactive oxygen species production , 2011, Proceedings of the National Academy of Sciences.

[34]  Simon C Watkins,et al.  Intra-mitochondrial Poly(ADP-ribosylation) Contributes to NAD+ Depletion and Cell Death Induced by Oxidative Stress* , 2003, The Journal of Biological Chemistry.

[35]  Eric Verdin,et al.  Mammalian Sir2 Homolog SIRT3 Regulates Global Mitochondrial Lysine Acetylation , 2007, Molecular and Cellular Biology.

[36]  S. Park,et al.  Sirt3-mediated deacetylation of evolutionarily conserved lysine 122 regulates MnSOD activity in response to stress. , 2010, Molecular cell.

[37]  Gene Kim,et al.  Sirt3 blocks the cardiac hypertrophic response by augmenting Foxo3a-dependent antioxidant defense mechanisms in mice. , 2009, The Journal of clinical investigation.

[38]  Guillaume Adelmant,et al.  Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1 , 2001, Nature.

[39]  J. Auwerx,et al.  PARP-1 inhibition increases mitochondrial metabolism through SIRT1 activation. , 2011, Cell metabolism.

[40]  B. Spiegelman,et al.  AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α , 2007, Proceedings of the National Academy of Sciences.

[41]  C. Deng,et al.  SIRT3 interacts with the daf-16 homolog FOXO3a in the Mitochondria, as well as increases FOXO3a Dependent Gene expression , 2008, International journal of biological sciences.

[42]  R. S. Sohal,et al.  Pro-oxidant shift in glutathione redox state during aging. , 2008, Advanced drug delivery reviews.

[43]  G. Shulman,et al.  Chronic activation of AMP kinase results in NRF-1 activation and mitochondrial biogenesis. , 2001, American journal of physiology. Endocrinology and metabolism.

[44]  M. Palacín,et al.  Evidence for a Mitochondrial Regulatory Pathway Defined by Peroxisome Proliferator–Activated Receptor-γ Coactivator-1α, Estrogen-Related Receptor-α, and Mitofusin 2 , 2006, Diabetes.

[45]  Keshav K. Singh Mitochondria Damage Checkpoint, Aging, and Cancer , 2006, Annals of the New York Academy of Sciences.

[46]  T. Nyström,et al.  Reducing mitochondrial fission results in increased life span and fitness of two fungal ageing models , 2007, Nature Cell Biology.

[47]  A. Cuervo,et al.  Autophagy gone awry in neurodegenerative diseases , 2010, Nature Neuroscience.

[48]  F. Alt,et al.  Tissue-specific regulation of SIRT 1 by calorie restriction , 2008 .

[49]  B. Corkey,et al.  Mitochondrial Networking Protects Beta Cells from Nutrient Induced Apoptosis , 2009 .

[50]  Howard T. Jacobs,et al.  Premature ageing in mice expressing defective mitochondrial DNA polymerase , 2004, Nature.

[51]  J. McGarry,et al.  Regulation of hepatic fatty acid oxidation and ketone body production. , 1980, Annual review of biochemistry.

[52]  H. Klocker,et al.  Identification and purification of a bovine liver mitochondrial NAD+‐glycohydrolase , 1995, FEBS letters.

[53]  R. Swanson,et al.  Poly(ADP-ribose) Polymerase-1-mediated Cell Death in Astrocytes Requires NAD+ Depletion and Mitochondrial Permeability Transition* , 2004, Journal of Biological Chemistry.

[54]  G. Carpenter Natural Selection , 1936, Nature.

[55]  S. Gygi,et al.  Succinate Dehydrogenase Is a Direct Target of Sirtuin 3 Deacetylase Activity , 2011, PloS one.

[56]  F. Alt,et al.  SIRT3 deacetylates mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase 2 and regulates ketone body production. , 2010, Cell metabolism.

[57]  B. Burgering,et al.  Cell cycle and death control: long live Forkheads. , 2002, Trends in biochemical sciences.

[58]  David P. Carney,et al.  Biochemical characterization, localization, and tissue distribution of the longer form of mouse SIRT3 , 2009, Protein science : a publication of the Protein Society.

[59]  O. Shirihai,et al.  Mitochondrial dynamics in the regulation of nutrient utilization and energy expenditure. , 2013, Cell metabolism.

[60]  E. Mervaala,et al.  Distinct Effects of Calorie Restriction and Resveratrol on Diet-Induced Obesity and Fatty Liver Formation , 2011, Journal of nutrition and metabolism.

[61]  Hideyuki Okano,et al.  Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice , 2006, Nature.

[62]  E. Dammer,et al.  Resveratrol stimulates cortisol biosynthesis by activating SIRT-dependent deacetylation of P450scc. , 2012, Endocrinology.

[63]  D. Reinberg,et al.  SIRT3 Functions in the Nucleus in the Control of Stress-Related Gene Expression , 2012, Molecular and Cellular Biology.

[64]  D. Gigot,et al.  Pre‐B‐cell colony‐enhancing factor, whose expression is up‐regulated in activated lymphocytes, is a nicotinamide phosphoribosyltransferase, a cytosolic enzyme involved in NAD biosynthesis , 2002, European journal of immunology.

[65]  L. Scorrano,et al.  Mitochondrial elongation during autophagy , 2011, Autophagy.

[66]  N. Sundaresan,et al.  Exogenous NAD Blocks Cardiac Hypertrophic Response via Activation of the SIRT3-LKB1-AMP-activated Kinase Pathway* , 2009, The Journal of Biological Chemistry.

[67]  M. Mattson,et al.  Defective DNA base excision repair in brain from individuals with Alzheimer's disease and amnestic mild cognitive impairment , 2007, Nucleic acids research.

[68]  P. C. Tapia,et al.  Sublethal mitochondrial stress with an attendant stoichiometric augmentation of reactive oxygen species may precipitate many of the beneficial alterations in cellular physiology produced by caloric restriction, intermittent fasting, exercise and dietary phytonutrients: "Mitohormesis" for health and , 2006, Medical hypotheses.

[69]  Shiwei Song,et al.  A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis , 2008, Proceedings of the National Academy of Sciences.

[70]  E. Verdin,et al.  Sirtuin regulation of mitochondria: energy production, apoptosis, and signaling. , 2010, Trends in biochemical sciences.

[71]  Jiandie D. Lin,et al.  Defects in Adaptive Energy Metabolism with CNS-Linked Hyperactivity in PGC-1α Null Mice , 2004, Cell.

[72]  J. N. Spelbrink,et al.  The human SIRT3 protein deacetylase is exclusively mitochondrial. , 2008, The Biochemical journal.

[73]  Michael Stumvoll,et al.  Antioxidants prevent health-promoting effects of physical exercise in humans , 2009, Proceedings of the National Academy of Sciences.

[74]  Marc Montminy,et al.  CREB regulates hepatic gluconeogenesis through the coactivator PGC-1 , 2001, Nature.

[75]  Ludivine Walter,et al.  The dynamin‐related protein DRP‐1 and the insulin signaling pathway cooperate to modulate Caenorhabditis elegans longevity , 2011, Aging cell.

[76]  C. Deng,et al.  SIRT3 is a mitochondria-localized tumor suppressor required for maintenance of mitochondrial integrity and metabolism during stress. , 2010, Cancer cell.

[77]  R. S. Sohal,et al.  Effects of age and caloric restriction on glutathione redox state in mice. , 2003, Free radical biology & medicine.

[78]  D. Accili,et al.  FoxOs at the Crossroads of Cellular Metabolism, Differentiation, and Transformation , 2004, Cell.

[79]  P. Bernardi,et al.  Mitochondrial transport of cations: channels, exchangers, and permeability transition. , 1999, Physiological reviews.

[80]  Dudley Lamming,et al.  Nutrient-Sensitive Mitochondrial NAD+ Levels Dictate Cell Survival , 2007, Cell.

[81]  C. Leeuwenburgh,et al.  New insights into the role of mitochondria in aging: mitochondrial dynamics and more , 2010, Journal of Cell Science.

[82]  Shujian Wei,et al.  Acetylation‐dependent regulation of mitochondrial ALDH2 activation by SIRT3 mediates acute ethanol‐induced eNOS activation , 2012, FEBS letters.

[83]  Wei Yu,et al.  Calorie restriction and SIRT3 trigger global reprogramming of the mitochondrial protein acetylome. , 2013, Molecular cell.

[84]  S. Rodríguez-Enríquez,et al.  Selective degradation of mitochondria by mitophagy. , 2007, Archives of biochemistry and biophysics.

[85]  V. Appanna,et al.  The Tricarboxylic Acid Cycle, an Ancient Metabolic Network with a Novel Twist , 2007, PloS one.

[86]  C. Deng,et al.  SIRT 3 interacts with the daf-16 homolog FOXO 3 a in the Mitochondria , as well as increases FOXO 3 a Dependent Gene expression , 2008 .

[87]  Johan Auwerx,et al.  Sirt5 Is a NAD-Dependent Protein Lysine Demalonylase and Desuccinylase , 2011, Science.

[88]  K. Morikawa,et al.  Acetyl-CoA Synthetase 2, a Mitochondrial Matrix Enzyme Involved in the Oxidation of Acetate* , 2001, The Journal of Biological Chemistry.

[89]  G. Perry,et al.  Oxidative Stress Increases Expression and Activity of BACE in NT2 Neurons , 2002, Neurobiology of Disease.

[90]  Robert V Farese,et al.  Sirt3 Regulates Fatty Acid Oxidation via Reversible Enzyme Deacetylation Hhs Public Access Supplementary Material , 2022 .

[91]  Robert S. Balaban,et al.  Mitochondria, Oxidants, and Aging , 2005, Cell.

[92]  N. Holbrook,et al.  Oxidants, oxidative stress and the biology of ageing , 2000, Nature.

[93]  C. Simone,et al.  A novel AMPK-dependent FoxO3A-SIRT3 intramitochondrial complex sensing glucose levels , 2013, Cellular and Molecular Life Sciences.

[94]  R E Burke,et al.  Apoptosis in neurodegenerative disorders. , 1997, Current opinion in neurology.

[95]  Katsuhiko Yano,et al.  FOXO3A genotype is strongly associated with human longevity , 2008, Proceedings of the National Academy of Sciences.

[96]  Robert V Farese,et al.  SIRT3 deficiency and mitochondrial protein hyperacetylation accelerate the development of the metabolic syndrome. , 2011, Molecular cell.

[97]  Eric Verdin,et al.  Reversible lysine acetylation controls the activity of the mitochondrial enzyme acetyl-CoA synthetase 2 , 2006, Proceedings of the National Academy of Sciences.

[98]  W. Ziolkowski,et al.  Effect of short-term ketogenic diet on redox status of human blood. , 2007, Rejuvenation research.

[99]  Huabing Zhang,et al.  Sirtuin 3, a New Target of PGC-1α, Plays an Important Role in the Suppression of ROS and Mitochondrial Biogenesis , 2010, PloS one.

[100]  H. Ranhotra,et al.  Up-regulation of orphan nuclear estrogen-related receptor alpha expression during long-term caloric restriction in mice , 2009, Molecular and Cellular Biochemistry.

[101]  T. Manini,et al.  The impact of aging on mitochondrial function and biogenesis pathways in skeletal muscle of sedentary high‐ and low‐functioning elderly individuals , 2012, Aging cell.

[102]  L. Oberley,et al.  An assay for superoxide dismutase activity in mammalian tissue homogenates. , 1989, Analytical biochemistry.

[103]  N. Sundaresan,et al.  SIRT3 Is a Stress-Responsive Deacetylase in Cardiomyocytes That Protects Cells from Stress-Mediated Cell Death by Deacetylation of Ku70 , 2008, Molecular and Cellular Biology.

[104]  Yu-Ting Wu,et al.  Regulation of mitochondrial F(o)F(1)ATPase activity by Sirt3-catalyzed deacetylation and its deficiency in human cells harboring 4977bp deletion of mitochondrial DNA. , 2013, Biochimica et biophysica acta.

[105]  W. C. Hallows,et al.  Sirtuins deacetylate and activate mammalian acetyl-CoA synthetases , 2006, Proceedings of the National Academy of Sciences.

[106]  J. G. Pastorino,et al.  Sirtuin-3 deacetylation of cyclophilin D induces dissociation of hexokinase II from the mitochondria , 2010, Journal of Cell Science.

[107]  Takeshi Tokuhisa,et al.  The role of autophagy during the early neonatal starvation period , 2004, Nature.

[108]  Jian-Hong Deng,et al.  NAD+-dependent Deacetylase SIRT3 Regulates Mitochondrial Protein Synthesis by Deacetylation of the Ribosomal Protein MRPL10* , 2009, The Journal of Biological Chemistry.

[109]  F. Alt,et al.  Tissue-specific regulation of SIRT1 by calorie restriction. , 2008, Genes & development.

[110]  M. Vreugdenhil,et al.  Calcium and normal brain ageing. , 2010, Cell calcium.

[111]  C. DeCarli,et al.  Midlife vascular risk factor exposure accelerates structural brain aging and cognitive decline , 2011, Alzheimer's & Dementia.

[112]  G. Perkins,et al.  Mitochondrial fragmentation in neurodegeneration , 2008, Nature Reviews Neuroscience.

[113]  K. Kouda,et al.  Beneficial effects of mild stress (hormetic effects): dietary restriction and health. , 2010, Journal of physiological anthropology.

[114]  Heng Du,et al.  Mitochondrial permeability transition pore in Alzheimer's disease: cyclophilin D and amyloid beta. , 2010, Biochimica et biophysica acta.

[115]  A. Holmgren,et al.  Thiol-based mechanisms of the thioredoxin and glutaredoxin systems: implications for diseases in the cardiovascular system. , 2007, American journal of physiology. Heart and circulatory physiology.

[116]  A. Feinberg,et al.  SIRT3, a human SIR2 homologue, is an NAD- dependent deacetylase localized to mitochondria , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[117]  C. Ross,et al.  trans-(−)-ϵ-Viniferin Increases Mitochondrial Sirtuin 3 (SIRT3), Activates AMP-activated Protein Kinase (AMPK), and Protects Cells in Models of Huntington Disease* , 2012, The Journal of Biological Chemistry.

[118]  Q. Tong,et al.  SIRT3, a Mitochondrial Sirtuin Deacetylase, Regulates Mitochondrial Function and Thermogenesis in Brown Adipocytes* , 2005, Journal of Biological Chemistry.

[119]  Q. Tong,et al.  Diet and exercise signals regulate SIRT3 and activate AMPK and PGC-1α in skeletal muscle , 2009, Aging.

[120]  J. Sastre,et al.  Oral administration of vitamin C decreases muscle mitochondrial biogenesis and hampers training-induced adaptations in endurance performance. , 2008, The American journal of clinical nutrition.

[121]  J. Kirkland Perspectives on cellular senescence and short term dietary restriction in adults , 2010, Aging.

[122]  J. Carlson,et al.  Changes in superoxide radical and lipid peroxide formation in the brain, heart and liver during the lifetime of the rat , 1987, Mechanisms of Ageing and Development.

[123]  M. Emond,et al.  Extension of Murine Life Span by Overexpression of Catalase Targeted to Mitochondria , 2005, Science.

[124]  B. Hyman,et al.  Pharmacological inhibition of PARP-1 reduces alpha-synuclein- and MPP+-induced cytotoxicity in Parkinson's disease in vitro models. , 2007, Biochemical and biophysical research communications.

[125]  Jiandie D. Lin,et al.  Suppression of Reactive Oxygen Species and Neurodegeneration by the PGC-1 Transcriptional Coactivators , 2006, Cell.

[126]  J. Lippincott-Schwartz,et al.  Fuse or die: Shaping mitochondrial fate during starvation , 2011, Communicative & integrative biology.

[127]  J. Milbrandt,et al.  Mitofusin 2 Is Necessary for Transport of Axonal Mitochondria and Interacts with the Miro/Milton Complex , 2010, The Journal of Neuroscience.

[128]  R. Weindruch,et al.  The retardation of aging in mice by dietary restriction: longevity, cancer, immunity and lifetime energy intake. , 1986, The Journal of nutrition.

[129]  E. Verdin,et al.  A New Splice Variant of the Mouse SIRT3 Gene Encodes the Mitochondrial Precursor Protein , 2009, PloS one.

[130]  S. Cuzzocrea,et al.  Cellular stress responses, hormetic phytochemicals and vitagenes in aging and longevity. , 2012, Biochimica et biophysica acta.

[131]  Jae Ho Park,et al.  Metabolomic analysis of livers and serum from high-fat diet induced obese mice. , 2011, Journal of proteome research.

[132]  D. Sinclair,et al.  Regulation of the mPTP by SIRT3-mediated deacetylation of CypD at lysine 166 suppresses age-related cardiac hypertrophy , 2010, Aging.

[133]  T. Theruvath,et al.  Mitochondrial calcium and the permeability transition in cell death. , 2009, Biochimica et biophysica acta.

[134]  D. Yarosh,et al.  Sirtuin 4 identification in normal human epidermal keratinocytes and its relation to sirtuin 3 and energy metabolism under normal conditions and UVB‐induced stress , 2012, Experimental dermatology.

[135]  C M McCay,et al.  The effect of retarded growth upon the length of life span and upon the ultimate body size. 1935. , 1935, Nutrition.

[136]  M. Palacín,et al.  Evidence for a mitochondrial regulatory pathway defined by peroxisome proliferator-activated receptor-gamma coactivator-1 alpha, estrogen-related receptor-alpha, and mitofusin 2. , 2006, Diabetes.

[137]  S. H. Kim,et al.  Neuronal Sirt3 Protects against Excitotoxic Injury in Mouse Cortical Neuron Culture , 2011, PloS one.

[138]  M. Anderson,et al.  Glutathione: an overview of biosynthesis and modulation. , 1998, Chemico-biological interactions.

[139]  O. Shirihai,et al.  Mitochondrial Networking Protects β-Cells From Nutrient-Induced Apoptosis , 2009, Diabetes.

[140]  David Carling,et al.  Supplemental Data LKB 1 Is the Upstream Kinase in the AMP-Activated Protein Kinase Cascade , 2003 .

[141]  F. Alt,et al.  SIRT4 Inhibits Glutamate Dehydrogenase and Opposes the Effects of Calorie Restriction in Pancreatic β Cells , 2006, Cell.

[142]  M. Mattson,et al.  Ceramide Protects Hippocampal Neurons Against Excitotoxic and Oxidative Insults, and Amyloid β‐Peptide Toxicity , 1996, Journal of neurochemistry.

[143]  S. Love,et al.  CNS SIRT3 Expression Is Altered by Reactive Oxygen Species and in Alzheimer’s Disease , 2012, PloS one.

[144]  R. Frye,et al.  Phylogenetic classification of prokaryotic and eukaryotic Sir2-like proteins. , 2000, Biochemical and biophysical research communications.

[145]  Lloyd M. Smith,et al.  Sirt3 promotes the urea cycle and fatty acid oxidation during dietary restriction. , 2011, Molecular cell.