Cargando…
Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration
Intervertebral disc degeneration (IVDD) is a predominant cause of disc herniation and is widespread worldwide. Inflammatory responses, mitochondrial dysfunction, and extracellular matrix degradation are known to be involved in IVDD. Scutellarin, an active ingredient extracted from Erigeron breviscap...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403485/ https://www.ncbi.nlm.nih.gov/pubmed/36032701 http://dx.doi.org/10.3389/fbioe.2022.883118 |
_version_ | 1784773387947606016 |
---|---|
author | Wang, Zihao Zhang, Pengfei Zhao, Yunpeng Yu, Feiran Wang, Shaoyi Liu, Kaiwen Cheng, Xiang Shi, Jie He, Qiting Xia, Yanni Cheng, Lei |
author_facet | Wang, Zihao Zhang, Pengfei Zhao, Yunpeng Yu, Feiran Wang, Shaoyi Liu, Kaiwen Cheng, Xiang Shi, Jie He, Qiting Xia, Yanni Cheng, Lei |
author_sort | Wang, Zihao |
collection | PubMed |
description | Intervertebral disc degeneration (IVDD) is a predominant cause of disc herniation and is widespread worldwide. Inflammatory responses, mitochondrial dysfunction, and extracellular matrix degradation are known to be involved in IVDD. Scutellarin, an active ingredient extracted from Erigeron breviscapus (Vaniot) Ha, Hand-Mazz, is reported to exhibit therapeutic potential in several degenerative diseases by suppressing inflammation and regulating metabolism. However, whether scutellarin can improve IVDD remains unknown. Human primary nucleus pulposus cells (HNPCs) were cultured and stimulated with TNF-α in the presence or absence of scutellarin. Furthermore, a rat needle puncture model was established, and scutellarin was injected into the IVD to verify its protective function against IVDD. Scutellarin attenuated the inflammatory reaction and retained the production of major IVD components both in vitro and in vivo. Mechanistically, scutellarin reduced the amount of reactive oxygen species (ROS), alleviated mitochondrial damage, and decreased the expression levels of apoptosis-related biomarkers upon stimulation with TNF-α. In addition, scutellarin antagonized the activation of the nuclear factor κ-light-chain-enhancer of activated B (NF-κB) signaling pathway and the mitogen-activated protein kinase (MAPK) signaling pathway and suppressed the activity of the NLRP3 inflammasome mediated by TNF-α. This study reveals that scutellarin protects against degeneration of nucleus pulposus cells, which might shed light on treatment of IVDD in the future. |
format | Online Article Text |
id | pubmed-9403485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94034852022-08-26 Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration Wang, Zihao Zhang, Pengfei Zhao, Yunpeng Yu, Feiran Wang, Shaoyi Liu, Kaiwen Cheng, Xiang Shi, Jie He, Qiting Xia, Yanni Cheng, Lei Front Bioeng Biotechnol Bioengineering and Biotechnology Intervertebral disc degeneration (IVDD) is a predominant cause of disc herniation and is widespread worldwide. Inflammatory responses, mitochondrial dysfunction, and extracellular matrix degradation are known to be involved in IVDD. Scutellarin, an active ingredient extracted from Erigeron breviscapus (Vaniot) Ha, Hand-Mazz, is reported to exhibit therapeutic potential in several degenerative diseases by suppressing inflammation and regulating metabolism. However, whether scutellarin can improve IVDD remains unknown. Human primary nucleus pulposus cells (HNPCs) were cultured and stimulated with TNF-α in the presence or absence of scutellarin. Furthermore, a rat needle puncture model was established, and scutellarin was injected into the IVD to verify its protective function against IVDD. Scutellarin attenuated the inflammatory reaction and retained the production of major IVD components both in vitro and in vivo. Mechanistically, scutellarin reduced the amount of reactive oxygen species (ROS), alleviated mitochondrial damage, and decreased the expression levels of apoptosis-related biomarkers upon stimulation with TNF-α. In addition, scutellarin antagonized the activation of the nuclear factor κ-light-chain-enhancer of activated B (NF-κB) signaling pathway and the mitogen-activated protein kinase (MAPK) signaling pathway and suppressed the activity of the NLRP3 inflammasome mediated by TNF-α. This study reveals that scutellarin protects against degeneration of nucleus pulposus cells, which might shed light on treatment of IVDD in the future. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9403485/ /pubmed/36032701 http://dx.doi.org/10.3389/fbioe.2022.883118 Text en Copyright © 2022 Wang, Zhang, Zhao, Yu, Wang, Liu, Cheng, Shi, He, Xia and Cheng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Wang, Zihao Zhang, Pengfei Zhao, Yunpeng Yu, Feiran Wang, Shaoyi Liu, Kaiwen Cheng, Xiang Shi, Jie He, Qiting Xia, Yanni Cheng, Lei Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title | Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title_full | Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title_fullStr | Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title_full_unstemmed | Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title_short | Scutellarin Protects Against Mitochondrial Reactive Oxygen Species-Dependent NLRP3 Inflammasome Activation to Attenuate Intervertebral Disc Degeneration |
title_sort | scutellarin protects against mitochondrial reactive oxygen species-dependent nlrp3 inflammasome activation to attenuate intervertebral disc degeneration |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403485/ https://www.ncbi.nlm.nih.gov/pubmed/36032701 http://dx.doi.org/10.3389/fbioe.2022.883118 |
work_keys_str_mv | AT wangzihao scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT zhangpengfei scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT zhaoyunpeng scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT yufeiran scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT wangshaoyi scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT liukaiwen scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT chengxiang scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT shijie scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT heqiting scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT xiayanni scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration AT chenglei scutellarinprotectsagainstmitochondrialreactiveoxygenspeciesdependentnlrp3inflammasomeactivationtoattenuateintervertebraldiscdegeneration |