Late- life shift in caloric intake affects fly longevity and metabolism

Caloric restriction (CR) delays the onset of age-related changes and extends lifespan in most species, but how late in life organisms benefit from switching to a low-calorie (L) diet is unexplored. We transferred wild type male flies from a high- (H) to a L-calorie diet (HL) or vice versa (LH) at different times. Late-life HL shift immediately and profoundly reduces fly mortality rate to briefly lower rate than in flies on a constant L diet, and increases lifespan. Conversely, a LH shift increases mortality and hazard rate, which is temporarily higher than in flies aged on a H diet, and leads to shorter lifespan. Transcriptomic changes within 48 hours following diet shift uncover physiological adaptations to available nutrients. Unexpectedly, more abundant transcriptomic changes accompanied LH shift, including ribosome biogenesis, and promotion of growth, which likely contributes to higher mortality rate. Considering that the beneficial effects of CR on physiology and lifespan are conserved across many organisms, our findings suggest that CR interventions in older humans may counteract the detrimental effects of H diets even when initiated later in life.

[1]  V. Longo,et al.  Nutrition, longevity and disease: From molecular mechanisms to interventions , 2022, Cell.

[2]  C. Heier,et al.  Drosophila Lipase 3 Mediates the Metabolic Response to Starvation and Aging , 2022, Frontiers in Aging.

[3]  T. Préat,et al.  Glia fuel neurons with locally synthesized ketone bodies to sustain memory under starvation , 2022, Nature Metabolism.

[4]  K. Lüersen,et al.  Phenotyping of Drosophila Melanogaster—A Nutritional Perspective , 2022, Biomolecules.

[5]  E. Giovannucci,et al.  Intermittent Fasting and Obesity-Related Health Outcomes , 2021, JAMA network open.

[6]  T. Chapman,et al.  Fitness benefits of dietary restriction , 2021, Proceedings of the Royal Society B.

[7]  Jared A Gatto,et al.  Circadian autophagy drives iTRF-mediated longevity , 2021, Nature.

[8]  G. Chawla,et al.  Evaluating the beneficial effects of dietary restrictions: A framework for precision nutrigeroscience. , 2021, Cell metabolism.

[9]  N. Perrimon,et al.  What fuels the fly: Energy metabolism in Drosophila and its application to the study of obesity and diabetes , 2021, Science Advances.

[10]  T. Wadden,et al.  Dietary interventions for obesity: clinical and mechanistic findings. , 2021, The Journal of clinical investigation.

[11]  M. Lehmann,et al.  Nuclear translocation ability of Lipin differentially affects gene expression and survival in fed and fasting Drosophila , 2020, Journal of Lipid Research.

[12]  M. Texada,et al.  Metabolism and growth adaptation to environmental conditions in Drosophila , 2020, Cellular and Molecular Life Sciences.

[13]  R. de Cabo,et al.  Untangling Determinants of Enhanced Health and Lifespan through a Multi-omics Approach in Mice. , 2020, Cell metabolism.

[14]  Corby K. Martin,et al.  Calorie restriction for enhanced longevity: The role of novel dietary strategies in the present obesogenic environment , 2020, Ageing Research Reviews.

[15]  M. Simons,et al.  The relationship between longevity and diet is genotype dependent and sensitive to desiccation in Drosophila melanogaster , 2020, Journal of Experimental Biology.

[16]  O. Hendrich,et al.  A nutritional memory effect counteracts benefits of dietary restriction in old mice , 2019, Nature Metabolism.

[17]  Peter L. Freddolino,et al.  Rapid metabolic shifts occur during the transition between hunger and satiety in Drosophila melanogaster , 2019, Nature Communications.

[18]  W. Kraus,et al.  2 years of calorie restriction and cardiometabolic risk (CALERIE): exploratory outcomes of a multicentre, phase 2, randomised controlled trial. , 2019, The lancet. Diabetes & endocrinology.

[19]  E. Ng’oma,et al.  Diverse biological processes coordinate the transcriptional response to nutritional changes in a Drosophila melanogaster multiparent population , 2019, BMC Genomics.

[20]  R. de Cabo,et al.  Daily Fasting Improves Health and Survival in Male Mice Independent of Diet Composition and Calories. , 2019, Cell metabolism.

[21]  R. de Cabo,et al.  A time to fast , 2018, Science.

[22]  L. Partridge,et al.  Short-Term, Intermittent Fasting Induces Long-Lasting Gut Health and TOR-Independent Lifespan Extension , 2018, Current Biology.

[23]  Corby K. Martin,et al.  Metabolic Slowing and Reduced Oxidative Damage with Sustained Caloric Restriction Support the Rate of Living and Oxidative Damage Theories of Aging. , 2018, Cell metabolism.

[24]  Matthew E. Talbert,et al.  RNA-Sequencing of Drosophila melanogaster Head Tissue on High-Sugar and High-Fat Diets , 2017, G3: Genes, Genomes, Genetics.

[25]  D. Sorenson,et al.  Merlin is required for coordinating proliferation of two stem cell lineages in the Drosophila testis , 2017, Scientific Reports.

[26]  O. Hendrich,et al.  Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism , 2017, Genome Biology.

[27]  B. Rogina,et al.  Rpd3 interacts with insulin signaling in Drosophila longevity extension , 2016, Aging.

[28]  B. Rudy,et al.  Drosophila SLC5A11 Mediates Hunger by Regulating K+ Channel Activity , 2016, Current Biology.

[29]  L. Ferrucci,et al.  Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice. , 2016, Cell metabolism.

[30]  W. Huber,et al.  Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 , 2014, Genome Biology.

[31]  S. Helfand,et al.  Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster , 2014, Aging.

[32]  B. Rogina,et al.  Determination of the spontaneous locomotor activity in Drosophila melanogaster. , 2014, Journal of visualized experiments : JoVE.

[33]  B. Rogina,et al.  Increased mitochondrial biogenesis preserves intestinal stem cell homeostasis and contributes to longevity in Indy mutant flies , 2014, Aging.

[34]  R. Weindruch,et al.  Caloric restriction reduces age-related and all-cause mortality in rhesus monkeys , 2014, Nature Communications.

[35]  Robert V Farese,et al.  Triacylglycerol synthesis enzymes mediate lipid droplet growth by relocalizing from the ER to lipid droplets. , 2013, Developmental cell.

[36]  W. Marzluff,et al.  Histones: Sequestered by Jabba in Fatty Storehouse , 2012, Current Biology.

[37]  David B. Allison,et al.  Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study , 2012, Nature.

[38]  Subhash D. Katewa,et al.  Intramyocellular fatty-acid metabolism plays a critical role in mediating responses to dietary restriction in Drosophila melanogaster. , 2012, Cell metabolism.

[39]  D. Jones,et al.  Stem Cell Dynamics in Response to Nutrient Availability , 2010, Current Biology.

[40]  Cyrus F. Khambatta,et al.  Calorie restriction increases fatty acid synthesis and whole body fat oxidation rates , 2010, American journal of physiology. Endocrinology and metabolism.

[41]  Chen-Yu Liao,et al.  Genetic variation in the murine lifespan response to dietary restriction: from life extension to life shortening , 2010, Aging cell.

[42]  B. Rogina,et al.  dSir2 mediates the increased spontaneous physical activity in flies on calorie restriction , 2009, Aging.

[43]  S. Pletcher,et al.  Dietary composition specifies consumption, obesity, and lifespan in Drosophila melanogaster , 2008, Aging cell.

[44]  R. de Cabo,et al.  Calorie restriction induces mitochondrial biogenesis and bioenergetic efficiency. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[45]  B. Rogina,et al.  Behavioral, physical, and demographic changes in Drosophila populations through dietary restriction , 2005, Aging cell.

[46]  S. Pletcher,et al.  Flies and their Golden Apples: The effect of dietary restriction on Drosophila aging and age-dependent gene expression , 2005, Ageing Research Reviews.

[47]  H. Jäckle,et al.  Brummer lipase is an evolutionary conserved fat storage regulator in Drosophila. , 2005, Cell metabolism.

[48]  L. Partridge,et al.  Dietary restriction, mortality trajectories, risk and damage , 2005, Mechanisms of Ageing and Development.

[49]  B. Rogina,et al.  Sir2 mediates longevity in the fly through a pathway related to calorie restriction. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[50]  J. Wood,et al.  Sirtuin activators mimic caloric restriction and delay ageing in metazoans , 2004, Nature.

[51]  S. Benzer,et al.  Regulation of Lifespan in Drosophila by Modulation of Genes in the TOR Signaling Pathway , 2004, Current Biology.

[52]  L. Partridge,et al.  Demography of Dietary Restriction and Death in Drosophila , 2003, Science.

[53]  David B. Goldstein,et al.  Genome-Wide Transcript Profiles in Aging and Calorically Restricted Drosophila melanogaster , 2002, Current Biology.

[54]  D. Grabowski,et al.  High Body Mass Index Does Not Predict Mortality in Older People: Analysis of the Longitudinal Study of Aging , 2001, Journal of the American Geriatrics Society.

[55]  M. Tatar,et al.  A Mutant Drosophila Insulin Receptor Homolog That Extends Life-Span and Impairs Neuroendocrine Function , 2001, Science.

[56]  E. Hafen,et al.  Extension of Life-Span by Loss of CHICO, a Drosophila Insulin Receptor Substrate Protein , 2001, Science.

[57]  S. Benzer,et al.  Preventing neurodegeneration in the Drosophila mutant bubblegum. , 1999, Science.

[58]  L. Partridge,et al.  Female fitness in Drosophila melanogaster: an interaction between the effect of nutrition and of encounter rate with males , 1996, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[59]  C. Kenyon,et al.  A C. elegans mutant that lives twice as long as wild type , 1993, Nature.