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Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses
Proanthocyanidins (PAC) are dietary compounds that have been extensively studied for beneficial health effects due to their anti-inflammatory properties. However, the structure-function relationships of PAC and their mode-of-action remain obscure. Here, we isolated a wide range of diverse PAC polyme...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295316/ https://www.ncbi.nlm.nih.gov/pubmed/34290357 http://dx.doi.org/10.1038/s42003-021-02408-3 |
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author | Andersen-Civil, Audrey Inge Schytz Leppä, Milla Marleena Thamsborg, Stig M. Salminen, Juha-Pekka Williams, Andrew R. |
author_facet | Andersen-Civil, Audrey Inge Schytz Leppä, Milla Marleena Thamsborg, Stig M. Salminen, Juha-Pekka Williams, Andrew R. |
author_sort | Andersen-Civil, Audrey Inge Schytz |
collection | PubMed |
description | Proanthocyanidins (PAC) are dietary compounds that have been extensively studied for beneficial health effects due to their anti-inflammatory properties. However, the structure-function relationships of PAC and their mode-of-action remain obscure. Here, we isolated a wide range of diverse PAC polymer mixtures of high purity from plant material. Polymer size was a key factor in determining the ability of PAC to regulate inflammatory cytokine responses in murine macrophages. PAC polymers with a medium (9.1) mean degree of polymerization (mDP) induced substantial transcriptomic changes, whereas PAC with either low (2.6) or high (12.3) mDP were significantly less active. Short-term oral treatment of mice with PAC modulated gene pathways connected to nutrient metabolism and inflammation in ileal tissue in a polymerization-dependent manner. Mechanistically, the bioactive PAC polymers modulated autophagic flux and inhibited lipopolysaccharide-induced autophagy in macrophages. Collectively, our results highlight the importance of defined structural features in the health-promoting effects of PAC-rich foods. |
format | Online Article Text |
id | pubmed-8295316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82953162021-08-12 Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses Andersen-Civil, Audrey Inge Schytz Leppä, Milla Marleena Thamsborg, Stig M. Salminen, Juha-Pekka Williams, Andrew R. Commun Biol Article Proanthocyanidins (PAC) are dietary compounds that have been extensively studied for beneficial health effects due to their anti-inflammatory properties. However, the structure-function relationships of PAC and their mode-of-action remain obscure. Here, we isolated a wide range of diverse PAC polymer mixtures of high purity from plant material. Polymer size was a key factor in determining the ability of PAC to regulate inflammatory cytokine responses in murine macrophages. PAC polymers with a medium (9.1) mean degree of polymerization (mDP) induced substantial transcriptomic changes, whereas PAC with either low (2.6) or high (12.3) mDP were significantly less active. Short-term oral treatment of mice with PAC modulated gene pathways connected to nutrient metabolism and inflammation in ileal tissue in a polymerization-dependent manner. Mechanistically, the bioactive PAC polymers modulated autophagic flux and inhibited lipopolysaccharide-induced autophagy in macrophages. Collectively, our results highlight the importance of defined structural features in the health-promoting effects of PAC-rich foods. Nature Publishing Group UK 2021-07-21 /pmc/articles/PMC8295316/ /pubmed/34290357 http://dx.doi.org/10.1038/s42003-021-02408-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Andersen-Civil, Audrey Inge Schytz Leppä, Milla Marleena Thamsborg, Stig M. Salminen, Juha-Pekka Williams, Andrew R. Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title | Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title_full | Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title_fullStr | Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title_full_unstemmed | Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title_short | Structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
title_sort | structure-function analysis of purified proanthocyanidins reveals a role for polymer size in suppressing inflammatory responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295316/ https://www.ncbi.nlm.nih.gov/pubmed/34290357 http://dx.doi.org/10.1038/s42003-021-02408-3 |
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