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Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice
Background: Polydatin is a stilbenoid with important antioxidant, anti-inflammatory, and immunomodulating properties. The aim of this study was to assess the anti-inflammatory preventive effect of polydatin in the mouse model of acute arthritis induced by calcium pyrophosphate (CPP) crystals. Method...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998880/ https://www.ncbi.nlm.nih.gov/pubmed/33805648 http://dx.doi.org/10.3390/nu13030929 |
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author | Oliviero, Francesca Galozzi, Paola Scanu, Anna Galuppini, Francesca Lazzarin, Vanni Brocco, Silvia Ravagnan, Giampietro Sfriso, Paolo Ramonda, Roberta Spinella, Paolo Punzi, Leonardo Pennelli, Gianmaria Luisetto, Roberto |
author_facet | Oliviero, Francesca Galozzi, Paola Scanu, Anna Galuppini, Francesca Lazzarin, Vanni Brocco, Silvia Ravagnan, Giampietro Sfriso, Paolo Ramonda, Roberta Spinella, Paolo Punzi, Leonardo Pennelli, Gianmaria Luisetto, Roberto |
author_sort | Oliviero, Francesca |
collection | PubMed |
description | Background: Polydatin is a stilbenoid with important antioxidant, anti-inflammatory, and immunomodulating properties. The aim of this study was to assess the anti-inflammatory preventive effect of polydatin in the mouse model of acute arthritis induced by calcium pyrophosphate (CPP) crystals. Methods: Acute arthritis was induced by the injection of a suspension of sterile CPP crystals into the ankle joint of Balb/c mice. Animals were randomized to receive polydatin or colchicine (the control drug) according to a prophylactic and a therapeutic protocol. The primary outcome was the variation of ankle swelling obtained after crystal injection and treatment, while histological parameters such as leukocyte infiltration, IL-1ß and CXCL1 levels and tissue expression were considered as secondary outcomes. Results: Prophylactic treatment with PD significantly diminished ankle swelling after 48 h from crystal injection. Secondary outcomes such as leukocyte infiltration, necrosis, edema, and synovitis were also decreased. PD caused a reduction in circulating levels of IL-1ß and CXCL1, as well as their tissue expression. By contrast, the therapeutic administration of PD did not have any beneficial effect. Conclusions: PD can effectively prevent acute inflammatory response to crystals in the mouse model of CPP crystal-induced arthritis. These results suggest that this bioactive compound might be used in the prevention of crystal-induced acute attacks in humans. |
format | Online Article Text |
id | pubmed-7998880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79988802021-03-28 Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice Oliviero, Francesca Galozzi, Paola Scanu, Anna Galuppini, Francesca Lazzarin, Vanni Brocco, Silvia Ravagnan, Giampietro Sfriso, Paolo Ramonda, Roberta Spinella, Paolo Punzi, Leonardo Pennelli, Gianmaria Luisetto, Roberto Nutrients Article Background: Polydatin is a stilbenoid with important antioxidant, anti-inflammatory, and immunomodulating properties. The aim of this study was to assess the anti-inflammatory preventive effect of polydatin in the mouse model of acute arthritis induced by calcium pyrophosphate (CPP) crystals. Methods: Acute arthritis was induced by the injection of a suspension of sterile CPP crystals into the ankle joint of Balb/c mice. Animals were randomized to receive polydatin or colchicine (the control drug) according to a prophylactic and a therapeutic protocol. The primary outcome was the variation of ankle swelling obtained after crystal injection and treatment, while histological parameters such as leukocyte infiltration, IL-1ß and CXCL1 levels and tissue expression were considered as secondary outcomes. Results: Prophylactic treatment with PD significantly diminished ankle swelling after 48 h from crystal injection. Secondary outcomes such as leukocyte infiltration, necrosis, edema, and synovitis were also decreased. PD caused a reduction in circulating levels of IL-1ß and CXCL1, as well as their tissue expression. By contrast, the therapeutic administration of PD did not have any beneficial effect. Conclusions: PD can effectively prevent acute inflammatory response to crystals in the mouse model of CPP crystal-induced arthritis. These results suggest that this bioactive compound might be used in the prevention of crystal-induced acute attacks in humans. MDPI 2021-03-13 /pmc/articles/PMC7998880/ /pubmed/33805648 http://dx.doi.org/10.3390/nu13030929 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Oliviero, Francesca Galozzi, Paola Scanu, Anna Galuppini, Francesca Lazzarin, Vanni Brocco, Silvia Ravagnan, Giampietro Sfriso, Paolo Ramonda, Roberta Spinella, Paolo Punzi, Leonardo Pennelli, Gianmaria Luisetto, Roberto Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title | Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title_full | Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title_fullStr | Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title_full_unstemmed | Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title_short | Polydatin Prevents Calcium Pyrophosphate Crystal-Induced Arthritis in Mice |
title_sort | polydatin prevents calcium pyrophosphate crystal-induced arthritis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998880/ https://www.ncbi.nlm.nih.gov/pubmed/33805648 http://dx.doi.org/10.3390/nu13030929 |
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