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Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway

CONTEXT: Osteoarthritis (OA) is a degenerative disease. Senkyunolide A (SenA) is an important phthalide from Ligusticum chuanxiong Hort (Umbelliferae) with anti-spasmodic and neuroprotective effects. OBJECTIVE: We explored the effect of SenA on IL-1β-stimulated chondrocytes and OA mice MATERIALS AND...

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Autores principales: Shao, Minglei, Lv, Dongwei, Zhou, Kai, Sun, Haijun, Wang, Zhitao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890578/
https://www.ncbi.nlm.nih.gov/pubmed/35225151
http://dx.doi.org/10.1080/13880209.2022.2042327
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author Shao, Minglei
Lv, Dongwei
Zhou, Kai
Sun, Haijun
Wang, Zhitao
author_facet Shao, Minglei
Lv, Dongwei
Zhou, Kai
Sun, Haijun
Wang, Zhitao
author_sort Shao, Minglei
collection PubMed
description CONTEXT: Osteoarthritis (OA) is a degenerative disease. Senkyunolide A (SenA) is an important phthalide from Ligusticum chuanxiong Hort (Umbelliferae) with anti-spasmodic and neuroprotective effects. OBJECTIVE: We explored the effect of SenA on IL-1β-stimulated chondrocytes and OA mice MATERIALS AND METHODS: Chondrocytes were stimulated by IL-1β (10 ng/mL) to establish an OA model in vitro. Cells were treated with SenA (20, 40, 80 and 160 μg/mL) for 48 h. The in vivo OA model was established by cutting off the medial meniscus tibial ligament (MMTL) at right knee incision of male C57BL/6 mice. One week after surgery, mice were injected with SenA (intraperitoneally one week) and divided into four groups (n = 6 per group): Sham, OA, OA + SenA 20 mg/kg and OA + SenA 40 mg/kg. The OA progression was examined by haematoxylin and eosin (H&E) staining. RESULTS: SenA treatment increased cell viability (33%), proliferation (71%), inhibited apoptosis (21%), decreased levels of catabolic marker proteins (MMP13, 23%; ADAMTS4, 31%; ADAMTS5, 19%), increased levels of anabolic marker proteins (IGF-1, 57%; aggrecan, 75%; Col2a1, 48%), reduced levels of inflammation cytokines (TNF-α, 31%; IL-6, 19%; IL-18, 20%) and decreased levels of NLRP3 (21%), ASC (20%) and caspase-1 (29%) of chondrocytes. However, NLRP3 agonist nigericin increased levels of MMP13 (55%), ADAMTS4 (70%), ADAMTS5 (53%), decreased levels of IGF-1 (36%), aggrecan (26%), Col2a1 (25%), inhibited proliferation (61%) and promoted apoptosis (76%). DISCUSSION AND CONCLUSIONS: SenA alleviates OA progression by inhibiting NLRP3 signalling pathways. These findings provide an experimental basis for the clinical application of drugs in the treatment of OA.
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spelling pubmed-88905782022-03-03 Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway Shao, Minglei Lv, Dongwei Zhou, Kai Sun, Haijun Wang, Zhitao Pharm Biol Research Article CONTEXT: Osteoarthritis (OA) is a degenerative disease. Senkyunolide A (SenA) is an important phthalide from Ligusticum chuanxiong Hort (Umbelliferae) with anti-spasmodic and neuroprotective effects. OBJECTIVE: We explored the effect of SenA on IL-1β-stimulated chondrocytes and OA mice MATERIALS AND METHODS: Chondrocytes were stimulated by IL-1β (10 ng/mL) to establish an OA model in vitro. Cells were treated with SenA (20, 40, 80 and 160 μg/mL) for 48 h. The in vivo OA model was established by cutting off the medial meniscus tibial ligament (MMTL) at right knee incision of male C57BL/6 mice. One week after surgery, mice were injected with SenA (intraperitoneally one week) and divided into four groups (n = 6 per group): Sham, OA, OA + SenA 20 mg/kg and OA + SenA 40 mg/kg. The OA progression was examined by haematoxylin and eosin (H&E) staining. RESULTS: SenA treatment increased cell viability (33%), proliferation (71%), inhibited apoptosis (21%), decreased levels of catabolic marker proteins (MMP13, 23%; ADAMTS4, 31%; ADAMTS5, 19%), increased levels of anabolic marker proteins (IGF-1, 57%; aggrecan, 75%; Col2a1, 48%), reduced levels of inflammation cytokines (TNF-α, 31%; IL-6, 19%; IL-18, 20%) and decreased levels of NLRP3 (21%), ASC (20%) and caspase-1 (29%) of chondrocytes. However, NLRP3 agonist nigericin increased levels of MMP13 (55%), ADAMTS4 (70%), ADAMTS5 (53%), decreased levels of IGF-1 (36%), aggrecan (26%), Col2a1 (25%), inhibited proliferation (61%) and promoted apoptosis (76%). DISCUSSION AND CONCLUSIONS: SenA alleviates OA progression by inhibiting NLRP3 signalling pathways. These findings provide an experimental basis for the clinical application of drugs in the treatment of OA. Taylor & Francis 2022-02-27 /pmc/articles/PMC8890578/ /pubmed/35225151 http://dx.doi.org/10.1080/13880209.2022.2042327 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://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/ (https://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
Shao, Minglei
Lv, Dongwei
Zhou, Kai
Sun, Haijun
Wang, Zhitao
Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title_full Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title_fullStr Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title_full_unstemmed Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title_short Senkyunolide A inhibits the progression of osteoarthritis by inhibiting the NLRP3 signalling pathway
title_sort senkyunolide a inhibits the progression of osteoarthritis by inhibiting the nlrp3 signalling pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890578/
https://www.ncbi.nlm.nih.gov/pubmed/35225151
http://dx.doi.org/10.1080/13880209.2022.2042327
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