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Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster
Modest dietary restriction extends lifespan (LS) in a diverse range of taxa and typically has a larger effect in females than males. Traditionally, this has been attributed to a stronger trade-off between LS and reproduction in females than in males that is mediated by the intake of calories. Recent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531074/ https://www.ncbi.nlm.nih.gov/pubmed/25808180 http://dx.doi.org/10.1111/acel.12333 |
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author | Jensen, Kim McClure, Colin Priest, Nicholas K Hunt, John |
author_facet | Jensen, Kim McClure, Colin Priest, Nicholas K Hunt, John |
author_sort | Jensen, Kim |
collection | PubMed |
description | Modest dietary restriction extends lifespan (LS) in a diverse range of taxa and typically has a larger effect in females than males. Traditionally, this has been attributed to a stronger trade-off between LS and reproduction in females than in males that is mediated by the intake of calories. Recent studies, however, suggest that it is the intake of specific nutrients that extends LS and mediates this trade-off. Here, we used the geometric framework (GF) to examine the sex-specific effects of protein (P) and carbohydrate (C) intake on LS and reproduction in Drosophila melanogaster. We found that LS was maximized at a high intake of C and a low intake of P in both sexes, whereas nutrient intake had divergent effects on reproduction. Male offspring production rate and LS were maximized at the same intake of nutrients, whereas female egg production rate was maximized at a high intake of diets with a P:C ratio of 1:2. This resulted in larger differences in nutrient-dependent optima for LS and reproduction in females than in males, as well as an optimal intake of nutrients for lifetime reproduction that differed between the sexes. Under dietary choice, the sexes followed similar feeding trajectories regulated around a P:C ratio of 1:4. Consequently, neither sex reached their nutritional optimum for lifetime reproduction, suggesting intralocus sexual conflict over nutrient optimization. Our study shows clear sex differences in the nutritional requirements of reproduction in D. melanogaster and joins the growing list of studies challenging the role of caloric restriction in extending LS. |
format | Online Article Text |
id | pubmed-4531074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45310742015-08-13 Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster Jensen, Kim McClure, Colin Priest, Nicholas K Hunt, John Aging Cell Original Articles Modest dietary restriction extends lifespan (LS) in a diverse range of taxa and typically has a larger effect in females than males. Traditionally, this has been attributed to a stronger trade-off between LS and reproduction in females than in males that is mediated by the intake of calories. Recent studies, however, suggest that it is the intake of specific nutrients that extends LS and mediates this trade-off. Here, we used the geometric framework (GF) to examine the sex-specific effects of protein (P) and carbohydrate (C) intake on LS and reproduction in Drosophila melanogaster. We found that LS was maximized at a high intake of C and a low intake of P in both sexes, whereas nutrient intake had divergent effects on reproduction. Male offspring production rate and LS were maximized at the same intake of nutrients, whereas female egg production rate was maximized at a high intake of diets with a P:C ratio of 1:2. This resulted in larger differences in nutrient-dependent optima for LS and reproduction in females than in males, as well as an optimal intake of nutrients for lifetime reproduction that differed between the sexes. Under dietary choice, the sexes followed similar feeding trajectories regulated around a P:C ratio of 1:4. Consequently, neither sex reached their nutritional optimum for lifetime reproduction, suggesting intralocus sexual conflict over nutrient optimization. Our study shows clear sex differences in the nutritional requirements of reproduction in D. melanogaster and joins the growing list of studies challenging the role of caloric restriction in extending LS. John Wiley & Sons, Ltd 2015-08 2015-03-23 /pmc/articles/PMC4531074/ /pubmed/25808180 http://dx.doi.org/10.1111/acel.12333 Text en © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Jensen, Kim McClure, Colin Priest, Nicholas K Hunt, John Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title | Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title_full | Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title_fullStr | Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title_full_unstemmed | Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title_short | Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster |
title_sort | sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in drosophila melanogaster |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531074/ https://www.ncbi.nlm.nih.gov/pubmed/25808180 http://dx.doi.org/10.1111/acel.12333 |
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