Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway
Abstract Osteoarthritis (OA) is a multi-factorial degenerative joint disease with unclear pathogenesis. Conservative treatments, primarily aimed at pain relief, fail to halt disease progression. Metabolic syndrome has recently been implicated in OA pathogenesis, underscoring the need for novel thera...
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Nature Portfolio
2025-01-01
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Online Access: | https://doi.org/10.1038/s41598-024-83993-1 |
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author | Jiale Mai Jiacong Xiao Yanhuai Ma Dawei Gong Jianliang Li |
author_facet | Jiale Mai Jiacong Xiao Yanhuai Ma Dawei Gong Jianliang Li |
author_sort | Jiale Mai |
collection | DOAJ |
description | Abstract Osteoarthritis (OA) is a multi-factorial degenerative joint disease with unclear pathogenesis. Conservative treatments, primarily aimed at pain relief, fail to halt disease progression. Metabolic syndrome has recently been implicated in OA pathogenesis, underscoring the need for novel therapeutic strategies. Arctiin (ARC), a lignan known for its anti-inflammatory and anti-osteoporotic properties, has potential effects on OA that merit exploration. We assessed ARC’s impact on chondrocyte viability using the Cell Counting Kit-8 and toluidine blue staining for glycosaminoglycan presence. Gene and protein expression were analyzed via RT-PCR, Western blotting, and immunofluorescence. An OA rat model was employed for in vivo evaluations through histological assessments and micro-CT scanning. ARC reversed IL-1β-induced upregulation of MMP3, MMP13, and COX-2 and the downregulation of collagen II and SOX9. It modulated cholesterol metabolism in IL-1β-stimulated chondrocytes by inhibiting the CH25H-CYP7B1-RORα axis, reducing cartilage damage and proteoglycan loss in OA rats, and effectively inhibiting subchondral bone osteolysis. ARC inhibits IL-1β-induced inflammatory responses and ECM degradation, suggesting its potential as a therapeutic agent for OA. It acts partly by modulating cholesterol metabolism and suppressing the CH25H/CYP7B1/RORα axis in chondrocytes. |
format | Article |
id | doaj-art-8bfa704b33d145b2b455863e44b00067 |
institution | Kabale University |
issn | 2045-2322 |
language | English |
publishDate | 2025-01-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Scientific Reports |
spelling | doaj-art-8bfa704b33d145b2b455863e44b000672025-01-05T12:18:54ZengNature PortfolioScientific Reports2045-23222025-01-0115111110.1038/s41598-024-83993-1Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathwayJiale Mai0Jiacong Xiao1Yanhuai Ma2Dawei Gong3Jianliang Li4Foshan Hospital of Traditional Chinese Medicine, Eighth Clinical School of Guangzhou University of Chinese MedicineFirst School of Clinical Medicine, Guangzhou University of Chinese MedicineDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Guangzhou University of Chinese MedicineDepartment of Orthopaedic Surgery, Wendeng Orthopedic and Traumatologic Hospital of Shandong ProvinceGuangzhou First People’s Hospital, the Second Affiliated Hospital, School of Medicine, South China University of Technology; Guangzhou First People’s Hospital, Guangzhou Medical UniversityAbstract Osteoarthritis (OA) is a multi-factorial degenerative joint disease with unclear pathogenesis. Conservative treatments, primarily aimed at pain relief, fail to halt disease progression. Metabolic syndrome has recently been implicated in OA pathogenesis, underscoring the need for novel therapeutic strategies. Arctiin (ARC), a lignan known for its anti-inflammatory and anti-osteoporotic properties, has potential effects on OA that merit exploration. We assessed ARC’s impact on chondrocyte viability using the Cell Counting Kit-8 and toluidine blue staining for glycosaminoglycan presence. Gene and protein expression were analyzed via RT-PCR, Western blotting, and immunofluorescence. An OA rat model was employed for in vivo evaluations through histological assessments and micro-CT scanning. ARC reversed IL-1β-induced upregulation of MMP3, MMP13, and COX-2 and the downregulation of collagen II and SOX9. It modulated cholesterol metabolism in IL-1β-stimulated chondrocytes by inhibiting the CH25H-CYP7B1-RORα axis, reducing cartilage damage and proteoglycan loss in OA rats, and effectively inhibiting subchondral bone osteolysis. ARC inhibits IL-1β-induced inflammatory responses and ECM degradation, suggesting its potential as a therapeutic agent for OA. It acts partly by modulating cholesterol metabolism and suppressing the CH25H/CYP7B1/RORα axis in chondrocytes.https://doi.org/10.1038/s41598-024-83993-1ArctiinOsteoarthritis treatmentChondrocyte metabolismAnti-inflammatory agentsSubchondral BoneCholesterol homeostasis |
spellingShingle | Jiale Mai Jiacong Xiao Yanhuai Ma Dawei Gong Jianliang Li Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway Scientific Reports Arctiin Osteoarthritis treatment Chondrocyte metabolism Anti-inflammatory agents Subchondral Bone Cholesterol homeostasis |
title | Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
title_full | Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
title_fullStr | Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
title_full_unstemmed | Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
title_short | Arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
title_sort | arctiin alleviates the progression of osteoarthritis by regulating the cholesterol metabolic pathway |
topic | Arctiin Osteoarthritis treatment Chondrocyte metabolism Anti-inflammatory agents Subchondral Bone Cholesterol homeostasis |
url | https://doi.org/10.1038/s41598-024-83993-1 |
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