题名 | Protocatechualdehyde inhibits receptor activator of nuclear factor kappa-B ligand-induced osteoclastogenesis and attenuates lipopolysaccharide-induced inflammatory osteolysis |
作者 | |
发表日期 | 2021-07 |
发表期刊 | PHYTOTHERAPY RESEARCH 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | anti‐ resorptives bone resorption ERK LPS osteoclast protocatechualdehyde |
其他关键词 | TUMOR-NECROSIS-FACTOR ; BONE-RESORPTION ; IN-VITRO ; GENE-EXPRESSION ; C-FOS ; PROTEIN-KINASE ; UP-REGULATION ; DIFFERENTIATION ; RANKL ; NFATC1 |
摘要 | Inflammatory osteolysis as a consequence of chronic bacterial infection underlies several lytic bone conditions, such as otitis media, osteomyelitis, septic arthritis, periodontitis, periprosthetic infection, and aseptic loosening of orthopedic implants. In consideration of the lack of effective preventive or treatments options against infectious osteolysis, the exploitation of novel pharmacological compounds/agents is critically required. The present study assessed the effect of protocatechualdehyde (PCA), a natural occurring polyphenolic compound with diverse biological activities including but not limited to antibacterial and antiinflammatory properties, on nuclear factor-kappa B ligand (RANKL)-induced osteoclastogenesis in vitro and lipopolysaccharide (LPS)-induced bone loss in vivo. In the present study, it was found that PCA potently inhibited RANKL-induced osteoclast formation, fusion, and activation toward bone resorption in a dose-dependent manner via the suppression of the ERK/c-Fos/nuclear factor of activated T-cells, cytoplasmic 1 signaling axis. It was further demonstrated that the in vivo administration of PCA could effectively protect mice against the deleterious effects of LPS-induced calvarial bone destruction by attenuating osteoclast formation and activity in a dose-dependent manner. Collectively, these findings provided evidence for the potential therapeutic application of PCA in the prevention and treatment of infectious osteolytic conditions, and potentially other osteoclast-mediated bone diseases. |
资助项目 | National Key Research and Development Program of China [2028YFC0310904] |
出版者 | WILEY |
出版地 | HOBOKEN |
ISSN | 0951-418X |
EISSN | 1099-1573 |
卷号 | 35期号:7页码:3821-3835 |
DOI | 10.1002/ptr.7088 |
页数 | 15 |
WOS类目 | Chemistry, Medicinal ; Pharmacology & Pharmacy |
WOS研究方向 | Pharmacology & Pharmacy |
WOS记录号 | WOS:000634006100001 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 33778997 |
SCOPUSEID | 2-s2.0-85103223515 |
通讯作者地址 | [Yuan, Jiandong]Department of Orthopedics,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China |
Scopus学科分类 | Pharmacology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/4904 |
专题 | 附属第一医院_骨科 其他_附属苍南医院(苍南县人民医院) |
通讯作者 | Yuan, Jiandong |
作者单位 | 1.Department of Orthopedics,Shaoxing People's Hospital (Shaoxing Hospital,Zhejiang University School of Medicine),Shaoxing,China; 2.Department of Biochemistry and Molecular Biology,College of Basic Medical,Navy Medical University,Shanghai,China; 3.Department of Orthopedics,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China; 4.Department of Orthopedics,The Affiliated Cangnan Hospital of Wenzhou Medical University,Wenzhou,China |
通讯作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
推荐引用方式 GB/T 7714 | Huang, Hao,Jiang, Wenli,Hong, Kehua,et al. Protocatechualdehyde inhibits receptor activator of nuclear factor kappa-B ligand-induced osteoclastogenesis and attenuates lipopolysaccharide-induced inflammatory osteolysis[J]. PHYTOTHERAPY RESEARCH,2021,35(7):3821-3835. |
APA | Huang, Hao., Jiang, Wenli., Hong, Kehua., Cai, Jie., He, Yongchao., ... & Yuan, Jiandong. (2021). Protocatechualdehyde inhibits receptor activator of nuclear factor kappa-B ligand-induced osteoclastogenesis and attenuates lipopolysaccharide-induced inflammatory osteolysis. PHYTOTHERAPY RESEARCH, 35(7), 3821-3835. |
MLA | Huang, Hao,et al."Protocatechualdehyde inhibits receptor activator of nuclear factor kappa-B ligand-induced osteoclastogenesis and attenuates lipopolysaccharide-induced inflammatory osteolysis".PHYTOTHERAPY RESEARCH 35.7(2021):3821-3835. |
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