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Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling

Early-life adversity is associated with accelerated cellular ageing during development and increased inflammation during adulthood. However, human studies can only establish correlation, not causation, and existing experimental animal approaches alter multiple components of early-life adversity simu...

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Autores principales: Nettle, Daniel, Andrews, Clare, Reichert, Sophie, Bedford, Tom, Kolenda, Claire, Parker, Craig, Martin-Ruiz, Carmen, Monaghan, Pat, Bateson, Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240102/
https://www.ncbi.nlm.nih.gov/pubmed/28094324
http://dx.doi.org/10.1038/srep40794
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author Nettle, Daniel
Andrews, Clare
Reichert, Sophie
Bedford, Tom
Kolenda, Claire
Parker, Craig
Martin-Ruiz, Carmen
Monaghan, Pat
Bateson, Melissa
author_facet Nettle, Daniel
Andrews, Clare
Reichert, Sophie
Bedford, Tom
Kolenda, Claire
Parker, Craig
Martin-Ruiz, Carmen
Monaghan, Pat
Bateson, Melissa
author_sort Nettle, Daniel
collection PubMed
description Early-life adversity is associated with accelerated cellular ageing during development and increased inflammation during adulthood. However, human studies can only establish correlation, not causation, and existing experimental animal approaches alter multiple components of early-life adversity simultaneously. We developed a novel hand-rearing paradigm in European starling nestlings (Sturnus vulgaris), in which we separately manipulated nutritional shortfall and begging effort for a period of 10 days. The experimental treatments accelerated erythrocyte telomere attrition and increased DNA damage measured in the juvenile period. For telomere attrition, amount of food and begging effort exerted additive effects. Only the combination of low food amount and high begging effort increased DNA damage. We then measured two markers of inflammation, high-sensitivity C-reactive protein and interleukin-6, when the birds were adults. The experimental treatments affected both inflammatory markers, though the patterns were complex and different for each marker. The effect of the experimental treatments on adult interleukin-6 was partially mediated by increased juvenile DNA damage. Our results show that both nutritional input and begging effort in the nestling period affect cellular ageing and adult inflammation in the starling. However, the pattern of effects is different for different biomarkers measured at different time points.
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spelling pubmed-52401022017-01-23 Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling Nettle, Daniel Andrews, Clare Reichert, Sophie Bedford, Tom Kolenda, Claire Parker, Craig Martin-Ruiz, Carmen Monaghan, Pat Bateson, Melissa Sci Rep Article Early-life adversity is associated with accelerated cellular ageing during development and increased inflammation during adulthood. However, human studies can only establish correlation, not causation, and existing experimental animal approaches alter multiple components of early-life adversity simultaneously. We developed a novel hand-rearing paradigm in European starling nestlings (Sturnus vulgaris), in which we separately manipulated nutritional shortfall and begging effort for a period of 10 days. The experimental treatments accelerated erythrocyte telomere attrition and increased DNA damage measured in the juvenile period. For telomere attrition, amount of food and begging effort exerted additive effects. Only the combination of low food amount and high begging effort increased DNA damage. We then measured two markers of inflammation, high-sensitivity C-reactive protein and interleukin-6, when the birds were adults. The experimental treatments affected both inflammatory markers, though the patterns were complex and different for each marker. The effect of the experimental treatments on adult interleukin-6 was partially mediated by increased juvenile DNA damage. Our results show that both nutritional input and begging effort in the nestling period affect cellular ageing and adult inflammation in the starling. However, the pattern of effects is different for different biomarkers measured at different time points. Nature Publishing Group 2017-01-17 /pmc/articles/PMC5240102/ /pubmed/28094324 http://dx.doi.org/10.1038/srep40794 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Nettle, Daniel
Andrews, Clare
Reichert, Sophie
Bedford, Tom
Kolenda, Claire
Parker, Craig
Martin-Ruiz, Carmen
Monaghan, Pat
Bateson, Melissa
Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title_full Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title_fullStr Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title_full_unstemmed Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title_short Early-life adversity accelerates cellular ageing and affects adult inflammation: Experimental evidence from the European starling
title_sort early-life adversity accelerates cellular ageing and affects adult inflammation: experimental evidence from the european starling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240102/
https://www.ncbi.nlm.nih.gov/pubmed/28094324
http://dx.doi.org/10.1038/srep40794
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