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A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model

Immunopathology corresponds to self-damage of the inflammatory response, resulting from oxidizing molecules produced when the immune system is activated. Immunopathology often contributes to age-related diseases and is believed to accelerate ageing. Prevention of immunopathology relies on endogenous...

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Autores principales: Dhinaut, Julien, Balourdet, Aude, Teixeira, Maria, Chogne, Manon, Moret, Yannick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622072/
https://www.ncbi.nlm.nih.gov/pubmed/28963510
http://dx.doi.org/10.1038/s41598-017-12769-7
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author Dhinaut, Julien
Balourdet, Aude
Teixeira, Maria
Chogne, Manon
Moret, Yannick
author_facet Dhinaut, Julien
Balourdet, Aude
Teixeira, Maria
Chogne, Manon
Moret, Yannick
author_sort Dhinaut, Julien
collection PubMed
description Immunopathology corresponds to self-damage of the inflammatory response, resulting from oxidizing molecules produced when the immune system is activated. Immunopathology often contributes to age-related diseases and is believed to accelerate ageing. Prevention of immunopathology relies on endogenous antioxidant enzymes and the consumption of dietary antioxidants, including carotenoids such as astaxanthin. Astaxanthin currently raises considerable interest as a powerful antioxidant and for its potential in alleviating age-related diseases. Current in vitro and short-term in vivo studies provide promising results about immune-stimulating and antioxidant properties of astaxanthin. However, to what extent dietary supplementation with astaxanthin can prevent long-term adverse effects of immunopathology on longevity is unknown so far. Here, using the mealworm beetle, Tenebrio molitor, as biological model we tested the effect of lifetime dietary supplementation with astaxanthin on longevity when exposed to early life inflammation. While supplementation with astaxanthin was found to lessen immunopathology cost on larval survival and insect longevity, it was also found to reduce immunity, growth rate and the survival of non immune-challenged larvae. This study therefore reveals that astaxanthin prevents immunopathology through an immune depressive effect and can have adverse consequences on growth.
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spelling pubmed-56220722017-10-12 A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model Dhinaut, Julien Balourdet, Aude Teixeira, Maria Chogne, Manon Moret, Yannick Sci Rep Article Immunopathology corresponds to self-damage of the inflammatory response, resulting from oxidizing molecules produced when the immune system is activated. Immunopathology often contributes to age-related diseases and is believed to accelerate ageing. Prevention of immunopathology relies on endogenous antioxidant enzymes and the consumption of dietary antioxidants, including carotenoids such as astaxanthin. Astaxanthin currently raises considerable interest as a powerful antioxidant and for its potential in alleviating age-related diseases. Current in vitro and short-term in vivo studies provide promising results about immune-stimulating and antioxidant properties of astaxanthin. However, to what extent dietary supplementation with astaxanthin can prevent long-term adverse effects of immunopathology on longevity is unknown so far. Here, using the mealworm beetle, Tenebrio molitor, as biological model we tested the effect of lifetime dietary supplementation with astaxanthin on longevity when exposed to early life inflammation. While supplementation with astaxanthin was found to lessen immunopathology cost on larval survival and insect longevity, it was also found to reduce immunity, growth rate and the survival of non immune-challenged larvae. This study therefore reveals that astaxanthin prevents immunopathology through an immune depressive effect and can have adverse consequences on growth. Nature Publishing Group UK 2017-09-29 /pmc/articles/PMC5622072/ /pubmed/28963510 http://dx.doi.org/10.1038/s41598-017-12769-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dhinaut, Julien
Balourdet, Aude
Teixeira, Maria
Chogne, Manon
Moret, Yannick
A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title_full A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title_fullStr A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title_full_unstemmed A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title_short A dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
title_sort dietary carotenoid reduces immunopathology and enhances longevity through an immune depressive effect in an insect model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622072/
https://www.ncbi.nlm.nih.gov/pubmed/28963510
http://dx.doi.org/10.1038/s41598-017-12769-7
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