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The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins
Dietary restriction (DR) extends life span across taxa. Despite considerable research, universal mechanisms of DR have not been identified, limiting its translational potential. Guided by the conviction that DR evolved as an adaptive, pro-longevity physiological response to food scarcity, biomedical...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034997/ https://www.ncbi.nlm.nih.gov/pubmed/32128403 http://dx.doi.org/10.1126/sciadv.aay3047 |
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author | McCracken, Andrew W. Adams, Gracie Hartshorne, Laura Tatar, Marc Simons, Mirre J. P. |
author_facet | McCracken, Andrew W. Adams, Gracie Hartshorne, Laura Tatar, Marc Simons, Mirre J. P. |
author_sort | McCracken, Andrew W. |
collection | PubMed |
description | Dietary restriction (DR) extends life span across taxa. Despite considerable research, universal mechanisms of DR have not been identified, limiting its translational potential. Guided by the conviction that DR evolved as an adaptive, pro-longevity physiological response to food scarcity, biomedical science has interpreted DR as an activator of pro-longevity molecular pathways. Current evolutionary theory predicts that organisms invest in their soma during DR, and thus when resource availability improves, should outcompete rich-fed controls in survival and/or reproduction. Testing this prediction in Drosophila melanogaster (N > 66,000 across 11 genotypes), our experiments revealed substantial, unexpected mortality costs when flies returned to a rich diet following DR. The physiological effects of DR should therefore not be interpreted as intrinsically pro-longevity, acting via somatic maintenance. We suggest DR could alternatively be considered an escape from costs incurred under nutrient-rich conditions, in addition to costs associated with DR. |
format | Online Article Text |
id | pubmed-7034997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70349972020-03-03 The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins McCracken, Andrew W. Adams, Gracie Hartshorne, Laura Tatar, Marc Simons, Mirre J. P. Sci Adv Research Articles Dietary restriction (DR) extends life span across taxa. Despite considerable research, universal mechanisms of DR have not been identified, limiting its translational potential. Guided by the conviction that DR evolved as an adaptive, pro-longevity physiological response to food scarcity, biomedical science has interpreted DR as an activator of pro-longevity molecular pathways. Current evolutionary theory predicts that organisms invest in their soma during DR, and thus when resource availability improves, should outcompete rich-fed controls in survival and/or reproduction. Testing this prediction in Drosophila melanogaster (N > 66,000 across 11 genotypes), our experiments revealed substantial, unexpected mortality costs when flies returned to a rich diet following DR. The physiological effects of DR should therefore not be interpreted as intrinsically pro-longevity, acting via somatic maintenance. We suggest DR could alternatively be considered an escape from costs incurred under nutrient-rich conditions, in addition to costs associated with DR. American Association for the Advancement of Science 2020-02-21 /pmc/articles/PMC7034997/ /pubmed/32128403 http://dx.doi.org/10.1126/sciadv.aay3047 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles McCracken, Andrew W. Adams, Gracie Hartshorne, Laura Tatar, Marc Simons, Mirre J. P. The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title | The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title_full | The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title_fullStr | The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title_full_unstemmed | The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title_short | The hidden costs of dietary restriction: Implications for its evolutionary and mechanistic origins |
title_sort | hidden costs of dietary restriction: implications for its evolutionary and mechanistic origins |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034997/ https://www.ncbi.nlm.nih.gov/pubmed/32128403 http://dx.doi.org/10.1126/sciadv.aay3047 |
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