Mifepristone Reduces Food Palatability and Affects Drosophila Feeding and Lifespan

The Drosophila GeneSwitch system facilitates the spatial and temporal control of gene expression through dietary supplementation of mifepristone (RU486). Because experimental and control groups differ only by treatment with RU486, confounding results from using flies of different genetic backgrounds are eliminated, making GeneSwitch especially useful in studies of aging. However, the effect of RU486 itself on longevity has not been well characterized, particularly in relation to nutritional states known to affect lifespan. Here, we show that RU486 has dose- and diet-dependent effects on longevity in both sexes. On low nutrient diets, RU486 supplementation reduces total food consumption, perhaps exacerbating undernutrition to shorten life. RU486 also inhibits proboscis extension responses to low nutrient diets, suggesting that RU486 has an aversive taste which leads to decreased food consumption and diminished longevity. RU486 is not detrimental to fly lifespan on high nutrient food, correlating with reduced effects of the drug on palatability and total consumption on rich diets. Our results highlight the critical importance of considering how food palatability and nutrient intake might be altered by dietary or drug manipulations in studies of aging and behavior.

[1]  S. Waddell,et al.  Remembering Nutrient Quality of Sugar in Drosophila , 2011, Current Biology.

[2]  E. Bernays,et al.  Post-ingestive feedbacks and associative learning regulate the intake of unsuitable sterols in a generalist grasshopper. , 1999, The Journal of experimental biology.

[3]  K. Hughes,et al.  Vitellogenin family gene expression does not increase Drosophila lifespan or fecundity , 2014, F1000Research.

[4]  S. Benzer,et al.  Water- and nutrient-dependent effects of dietary restriction on Drosophila lifespan , 2009, Proceedings of the National Academy of Sciences.

[5]  Tetsuya Miyamoto,et al.  A Fructose Receptor Functions as a Nutrient Sensor in the Drosophila Brain , 2012, Cell.

[6]  M. Gordon,et al.  Pharyngeal sense organs drive robust sugar consumption in Drosophila , 2015, Nature Communications.

[7]  Severine Trannoy,et al.  The steroid hormone receptor EcR finely modulates Drosophila lifespan during adulthood in a sex-specific manner , 2009, Mechanisms of Ageing and Development.

[8]  Ronald L. Davis,et al.  P{Switch}, a system for spatial and temporal control of gene expression in Drosophila melanogaster , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Jaehyoung Cho,et al.  Extension of Drosophila Life Span by RNAi of the Mitochondrial Respiratory Chain , 2009, Current Biology.

[10]  S. Tavaré,et al.  A screen of apoptosis and senescence regulatory genes for life span effects when over-expressed in Drosophila , 2009, Aging.

[11]  S. Zou,et al.  Nutraceutical Interventions for Promoting Healthy Aging in Invertebrate Models , 2012, Oxidative medicine and cellular longevity.

[12]  S. Tavaré,et al.  Drosophila melanogaster p53 has developmental stage-specific and sex-specific effects on adult life span indicative of sexual antagonistic pleiotropy , 2009, Aging.

[13]  J. Tower,et al.  Alteration of Drosophila life span using conditional, tissue-specific expression of transgenes triggered by doxycyline or RU486/Mifepristone , 2007, Experimental Gerontology.

[14]  N. Perrimon,et al.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. , 1993, Development.

[15]  Benjamin H. White,et al.  A conditional tissue-specific transgene expression system using inducible GAL4 , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Linda Partridge,et al.  Benchmarks for ageing studies , 2007, Nature.

[17]  J. Winter Practical Assessment, Research, and Evaluation Practical Assessment, Research, and Evaluation Using the Student's t-test with extremely small sample sizes Using the Student's t-test with extremely small sample sizes , 2022 .

[18]  Jae-Seong Yang,et al.  OASIS: Online Application for the Survival Analysis of Lifespan Assays Performed in Aging Research , 2011, PloS one.

[19]  L. Partridge,et al.  Calories Do Not Explain Extension of Life Span by Dietary Restriction in Drosophila , 2005, PLoS biology.

[20]  F. Marion-Poll,et al.  Dual Mechanism for Bitter Avoidance in Drosophila , 2015, The Journal of Neuroscience.

[21]  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.

[22]  Soohong Min,et al.  Taste-independent detection of the caloric content of sugar in Drosophila , 2011, Proceedings of the National Academy of Sciences.

[23]  E. Schmelz,et al.  Interactions between Spinacia oleracea and Bradysia impatiens: a role for phytoecdysteroids. , 2002, Archives of insect biochemistry and physiology.

[24]  M. Jafari Drosophila melanogaster as a model system for the evaluation of anti-aging compounds , 2010, Fly.

[25]  J. Tower,et al.  The progesterone antagonist mifepristone/RU486 blocks the negative effect on life span caused by mating in female Drosophila , 2015, Aging.

[26]  Alex Zhavoronkov,et al.  Lifespan and Stress Resistance in Drosophila with Overexpressed DNA Repair Genes , 2015, Scientific Reports.

[27]  L. Partridge,et al.  Dietary restriction in Drosophila , 2005, Mechanisms of Ageing and Development.

[28]  Jeffrey W Stafford,et al.  Integration of Taste and Calorie Sensing in Drosophila , 2012, The Journal of Neuroscience.

[29]  R. Lehmann,et al.  Lifespan Extension by Preserving Proliferative Homeostasis in Drosophila , 2010, PLoS genetics.

[30]  Subhash D. Katewa,et al.  4E-BP Extends Lifespan upon Dietary Restriction by Enhancing Mitochondrial Activity in Drosophila , 2009, Cell.

[31]  C. Montell,et al.  An Odorant-Binding Protein Required for Suppression of Sweet Taste by Bitter Chemicals , 2013, Neuron.

[32]  J. Carlson,et al.  Proboscis extension response (PER) assay in Drosophila. , 2007, Journal of visualized experiments : JoVE.

[33]  C. Zeng,et al.  Gender-specific prandial response to dietary restriction and oxidative stress in Drosophila melanogaster , 2011, Fly.

[34]  R. Yamada,et al.  Microbes Promote Amino Acid Harvest to Rescue Undernutrition in Drosophila. , 2015, Cell reports.

[35]  D. Reed,et al.  "A spoonful of sugar helps the medicine go down": bitter masking by sucrose among children and adults. , 2015, Chemical senses.

[36]  J. D. de Winter Using the Student ’ s t-test with extremely small sample sizes , 2013 .

[37]  D. Walker,et al.  AMPK modulates tissue and organismal aging in a non-cell-autonomous manner. , 2014, Cell reports.

[38]  Sany Hoxha,et al.  Acidic Food pH Increases Palatability and Consumption and Extends Drosophila Lifespan. , 2015, The Journal of nutrition.

[39]  S. Benzer,et al.  Compensatory ingestion upon dietary restriction in Drosophila melanogaster , 2005, Nature Methods.

[40]  David Raubenheimer,et al.  Lifespan and reproduction in Drosophila: New insights from nutritional geometry , 2008, Proceedings of the National Academy of Sciences.

[41]  A. Vilcinskas,et al.  The Fruit Fly Drosophila melanogaster as a Model for Aging Research. , 2013, Advances in biochemical engineering/biotechnology.

[42]  T. Tanimura,et al.  Drosophila Evaluates and Learns the Nutritional Value of Sugars , 2011, Current Biology.

[43]  P. Kapahi,et al.  High carbohydrate–low protein consumption maximizes Drosophila lifespan , 2013, Experimental Gerontology.

[44]  K. Lee Dietary protein:carbohydrate balance is a critical modulator of lifespan and reproduction in Drosophila melanogaster: a test using a chemically defined diet. , 2015, Journal of insect physiology.

[45]  S. Benzer,et al.  Prandiology of Drosophila and the CAFE assay , 2007, Proceedings of the National Academy of Sciences.

[46]  T. Andrews,et al.  Interplay of dFOXO and Two ETS-Family Transcription Factors Determines Lifespan in Drosophila melanogaster , 2014, PLoS genetics.

[47]  D. Walker,et al.  Perturbation of mitochondrial complex V alters the response to dietary restriction in Drosophila , 2010, Aging cell.

[48]  S. Simpson,et al.  The nature of nutrition: a unifying framework , 2011 .

[49]  Gil B. Carvalho,et al.  Quantifying Drosophila food intake: comparative analysis of current methodology , 2014, Nature Methods.