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Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats

Context: Rheumatoid arthritis (RA) is a common systemic auto-immune disease, which is characterized by chronic and symmetry synovial inflammation. Crocin has been reported to exhibit anti-inflammatory effects in animal models. Objective: This study investigates the anti-inflammatory and anti-arthrit...

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Autores principales: Liu, Wei, Sun, Yufeng, Cheng, Zhenping, Guo, Yong, Liu, Peiming, Wen, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168764/
https://www.ncbi.nlm.nih.gov/pubmed/29540097
http://dx.doi.org/10.1080/13880209.2018.1448874
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author Liu, Wei
Sun, Yufeng
Cheng, Zhenping
Guo, Yong
Liu, Peiming
Wen, Ying
author_facet Liu, Wei
Sun, Yufeng
Cheng, Zhenping
Guo, Yong
Liu, Peiming
Wen, Ying
author_sort Liu, Wei
collection PubMed
description Context: Rheumatoid arthritis (RA) is a common systemic auto-immune disease, which is characterized by chronic and symmetry synovial inflammation. Crocin has been reported to exhibit anti-inflammatory effects in animal models. Objective: This study investigates the anti-inflammatory and anti-arthritic effects of crocin on type II collagen-induced arthritis (CIA) in Wistar rats. Materials and methods: The CIA rat model was established and randomly divided into five groups with or without crocin treatment (10, 20 or 40 mg/kg), which was started on day 21 after arthritis induction and persisted for 36 days. The symptoms and molecular mechanisms of CIA and crocin-treated CIA rats were compared and investigated. Results: CIA rats presented severe RA symptoms, including high arthritis score, paw swelling, joint inflammation, bone erosion, chondrocyte death, cartilage destruction, enhanced expressions of matrix metalloproteinase (MMP) and pro-inflammatory cytokines. However, crocin could mitigate these symptoms. Crocin (40 mg/kg) exhibited the most efficient therapeutic function on CIA rats: the histological scores of joint inflammation, bone erosion, chondrocyte death, cartilage surface erosion, and bone erosion of CIA rats receiving 40 mg/kg crocin treatment were comparable to the normal rats. MMP-1, -3 and -13 protein expression levels of CIA rats with 40 mg/kg crocin treatment were decreased to levels similar to normal rats. Moreover, crocin could also inhibit the expression of TNF-α, IL-17, IL-6 and CXCL8 in serum and ankle tissues of CIA rats. Conclusions: In summary, crocin exhibits therapeutic potential for RA, by mitigating the symptoms and inhibiting the pro-inflammatory factor expression.
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spelling pubmed-61687642018-10-04 Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats Liu, Wei Sun, Yufeng Cheng, Zhenping Guo, Yong Liu, Peiming Wen, Ying Pharm Biol Research Article Context: Rheumatoid arthritis (RA) is a common systemic auto-immune disease, which is characterized by chronic and symmetry synovial inflammation. Crocin has been reported to exhibit anti-inflammatory effects in animal models. Objective: This study investigates the anti-inflammatory and anti-arthritic effects of crocin on type II collagen-induced arthritis (CIA) in Wistar rats. Materials and methods: The CIA rat model was established and randomly divided into five groups with or without crocin treatment (10, 20 or 40 mg/kg), which was started on day 21 after arthritis induction and persisted for 36 days. The symptoms and molecular mechanisms of CIA and crocin-treated CIA rats were compared and investigated. Results: CIA rats presented severe RA symptoms, including high arthritis score, paw swelling, joint inflammation, bone erosion, chondrocyte death, cartilage destruction, enhanced expressions of matrix metalloproteinase (MMP) and pro-inflammatory cytokines. However, crocin could mitigate these symptoms. Crocin (40 mg/kg) exhibited the most efficient therapeutic function on CIA rats: the histological scores of joint inflammation, bone erosion, chondrocyte death, cartilage surface erosion, and bone erosion of CIA rats receiving 40 mg/kg crocin treatment were comparable to the normal rats. MMP-1, -3 and -13 protein expression levels of CIA rats with 40 mg/kg crocin treatment were decreased to levels similar to normal rats. Moreover, crocin could also inhibit the expression of TNF-α, IL-17, IL-6 and CXCL8 in serum and ankle tissues of CIA rats. Conclusions: In summary, crocin exhibits therapeutic potential for RA, by mitigating the symptoms and inhibiting the pro-inflammatory factor expression. Taylor & Francis 2018-03-15 /pmc/articles/PMC6168764/ /pubmed/29540097 http://dx.doi.org/10.1080/13880209.2018.1448874 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Wei
Sun, Yufeng
Cheng, Zhenping
Guo, Yong
Liu, Peiming
Wen, Ying
Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title_full Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title_fullStr Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title_full_unstemmed Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title_short Crocin exerts anti-inflammatory and anti-arthritic effects on type II collagen-induced arthritis in rats
title_sort crocin exerts anti-inflammatory and anti-arthritic effects on type ii collagen-induced arthritis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168764/
https://www.ncbi.nlm.nih.gov/pubmed/29540097
http://dx.doi.org/10.1080/13880209.2018.1448874
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