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Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma
BACKGROUND: The paternal diet affects lipid metabolism in offspring for at least two generations through nutritional programming. However, we do not know how this is propagated to the offspring. OBJECTIVES: We tested the hypothesis that the changes in lipid metabolism that are driven by paternal die...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828597/ https://www.ncbi.nlm.nih.gov/pubmed/35141784 http://dx.doi.org/10.1007/s11306-022-01869-9 |
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author | Furse, Samuel Watkins, Adam J. Williams, Huw E. L. Snowden, Stuart G. Chiarugi, Davide Koulman, Albert |
author_facet | Furse, Samuel Watkins, Adam J. Williams, Huw E. L. Snowden, Stuart G. Chiarugi, Davide Koulman, Albert |
author_sort | Furse, Samuel |
collection | PubMed |
description | BACKGROUND: The paternal diet affects lipid metabolism in offspring for at least two generations through nutritional programming. However, we do not know how this is propagated to the offspring. OBJECTIVES: We tested the hypothesis that the changes in lipid metabolism that are driven by paternal diet are propagated through spermatozoa and not seminal plasma. METHODS: We applied an updated, purpose-built computational network analysis tool to characterise control of lipid metabolism systemically (Lipid Traffic Analysis v2.3) on a known mouse model of paternal nutritional programming. RESULTS: The analysis showed that the two possible routes for programming effects, the sperm (genes) and seminal plasma (influence on the uterine environment), both have a distinct effect on the offspring’s lipid metabolism. Further, the programming effects in offspring suggest that changes in lipid distribution are more important than alterations in lipid biosynthesis. CONCLUSIONS: These results show how the uterine environment and genes both affect lipid metabolism in offspring, enhancing our understanding of the link between parental diet and metabolism in offspring. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-022-01869-9. |
format | Online Article Text |
id | pubmed-8828597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-88285972022-02-22 Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma Furse, Samuel Watkins, Adam J. Williams, Huw E. L. Snowden, Stuart G. Chiarugi, Davide Koulman, Albert Metabolomics Original Article BACKGROUND: The paternal diet affects lipid metabolism in offspring for at least two generations through nutritional programming. However, we do not know how this is propagated to the offspring. OBJECTIVES: We tested the hypothesis that the changes in lipid metabolism that are driven by paternal diet are propagated through spermatozoa and not seminal plasma. METHODS: We applied an updated, purpose-built computational network analysis tool to characterise control of lipid metabolism systemically (Lipid Traffic Analysis v2.3) on a known mouse model of paternal nutritional programming. RESULTS: The analysis showed that the two possible routes for programming effects, the sperm (genes) and seminal plasma (influence on the uterine environment), both have a distinct effect on the offspring’s lipid metabolism. Further, the programming effects in offspring suggest that changes in lipid distribution are more important than alterations in lipid biosynthesis. CONCLUSIONS: These results show how the uterine environment and genes both affect lipid metabolism in offspring, enhancing our understanding of the link between parental diet and metabolism in offspring. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-022-01869-9. Springer US 2022-02-10 2022 /pmc/articles/PMC8828597/ /pubmed/35141784 http://dx.doi.org/10.1007/s11306-022-01869-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Furse, Samuel Watkins, Adam J. Williams, Huw E. L. Snowden, Stuart G. Chiarugi, Davide Koulman, Albert Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title | Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title_full | Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title_fullStr | Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title_full_unstemmed | Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title_short | Paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
title_sort | paternal nutritional programming of lipid metabolism is propagated through sperm and seminal plasma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828597/ https://www.ncbi.nlm.nih.gov/pubmed/35141784 http://dx.doi.org/10.1007/s11306-022-01869-9 |
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