Cargando…

A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway

[Image: see text] Synovium has widely participated in induced inflammation, suggesting that it is a potential target to reduce aromatase inhibitors (AIs) causing joint inflammation or pain. Exercise and mechanical stimulation are important strategies for precaution and treatment of bone inflammation...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Zipeng, Xu, Chang-Peng, Chen, Yuhui, Li, Wenqiang, Wang, Liping, Yuan, Zi-Guo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153782/
https://www.ncbi.nlm.nih.gov/pubmed/34056178
http://dx.doi.org/10.1021/acsomega.1c00580
_version_ 1783698875295465472
author Yang, Zipeng
Xu, Chang-Peng
Chen, Yuhui
Li, Wenqiang
Wang, Liping
Yuan, Zi-Guo
author_facet Yang, Zipeng
Xu, Chang-Peng
Chen, Yuhui
Li, Wenqiang
Wang, Liping
Yuan, Zi-Guo
author_sort Yang, Zipeng
collection PubMed
description [Image: see text] Synovium has widely participated in induced inflammation, suggesting that it is a potential target to reduce aromatase inhibitors (AIs) causing joint inflammation or pain. Exercise and mechanical stimulation are important strategies for precaution and treatment of bone inflammation. In this work, we developed a novel thermo-sensitive hydrogel, which could be injected intra-articularly. The aim of this research was to investigate the role of various mechanical strength hydrogels in reducing synovium inflammation. The effect of different mechanical strength hydrogels on regulating synovium inflammation was used to stimulate human fibroblast-like synoviocytes (FLS) under a cyclic mechanical compression environment in vitro. Cytokine and metalloprotease expression in FLS was analyzed by the western blot and q-PCR method, in which FLS were cultured with the different mechanical strength hydrogels. The results showed that a moderate-intensity hydrogel mechanical stimulation might be suitable in reducing AI-induced FLS inflammation via the NK-κB pathway. In addition, we built an AI-treated rat model and injected the different mechanical strength hydrogels. Similarly, the moderate-strength mechanical hydrogel could reduce the inflammatory factor and metalloproteinase expression in synovial tissues and intra-articular synovia.
format Online
Article
Text
id pubmed-8153782
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-81537822021-05-27 A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway Yang, Zipeng Xu, Chang-Peng Chen, Yuhui Li, Wenqiang Wang, Liping Yuan, Zi-Guo ACS Omega [Image: see text] Synovium has widely participated in induced inflammation, suggesting that it is a potential target to reduce aromatase inhibitors (AIs) causing joint inflammation or pain. Exercise and mechanical stimulation are important strategies for precaution and treatment of bone inflammation. In this work, we developed a novel thermo-sensitive hydrogel, which could be injected intra-articularly. The aim of this research was to investigate the role of various mechanical strength hydrogels in reducing synovium inflammation. The effect of different mechanical strength hydrogels on regulating synovium inflammation was used to stimulate human fibroblast-like synoviocytes (FLS) under a cyclic mechanical compression environment in vitro. Cytokine and metalloprotease expression in FLS was analyzed by the western blot and q-PCR method, in which FLS were cultured with the different mechanical strength hydrogels. The results showed that a moderate-intensity hydrogel mechanical stimulation might be suitable in reducing AI-induced FLS inflammation via the NK-κB pathway. In addition, we built an AI-treated rat model and injected the different mechanical strength hydrogels. Similarly, the moderate-strength mechanical hydrogel could reduce the inflammatory factor and metalloproteinase expression in synovial tissues and intra-articular synovia. American Chemical Society 2021-04-10 /pmc/articles/PMC8153782/ /pubmed/34056178 http://dx.doi.org/10.1021/acsomega.1c00580 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Yang, Zipeng
Xu, Chang-Peng
Chen, Yuhui
Li, Wenqiang
Wang, Liping
Yuan, Zi-Guo
A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title_full A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title_fullStr A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title_full_unstemmed A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title_short A Novel Mechanical-Based Injective Hydrogel for Treatment with Aromatase Inhibitors Caused Joint Inflammation via the NF-κB Pathway
title_sort novel mechanical-based injective hydrogel for treatment with aromatase inhibitors caused joint inflammation via the nf-κb pathway
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153782/
https://www.ncbi.nlm.nih.gov/pubmed/34056178
http://dx.doi.org/10.1021/acsomega.1c00580
work_keys_str_mv AT yangzipeng anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT xuchangpeng anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT chenyuhui anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT liwenqiang anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT wangliping anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT yuanziguo anovelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT yangzipeng novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT xuchangpeng novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT chenyuhui novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT liwenqiang novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT wangliping novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway
AT yuanziguo novelmechanicalbasedinjectivehydrogelfortreatmentwitharomataseinhibitorscausedjointinflammationviathenfkbpathway