Sequential anti-inflammatory and osteogenic effects of a dual drug delivery scaffold loaded with parthenolide and naringin in periodontitis

被引:3
|
作者
Chen, Rui [1 ,2 ]
Wang, Mengting [1 ,2 ]
Qi, Qiaoling [3 ]
Tang, Yanli [1 ,2 ]
Guo, Zhenzhao [4 ]
Wu, Shuai [4 ]
Li, Qiyan [1 ,2 ,5 ]
机构
[1] First Peoples Hosp Yunnan Prov, Dept Stomatol, Kunming, Peoples R China
[2] Kunming Univ Sci & Technol, Affiliated Hosp, Kunming, Peoples R China
[3] Dali Univ, Yunnan Prov Key Lab Entomol Biopharmaceut R&D, Dali, Peoples R China
[4] Jinan Univ, Guangzhou, Peoples R China
[5] First Peoples Hosp Yunnan Prov, Dept Stomatol, 157 Jinbi St, Kunming 650032, Yunnan, Peoples R China
来源
关键词
Drug delivery systems; Naringin; Parthenolide; Periodontitis; WEB-SERVER; KAPPA-B; BONE; IDENTIFICATION; REGENERATION; PREDICTION; GENE; MICE;
D O I
10.5051/jpis.2105700285
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Our pilot study showed that a 3-dimensional dual drug delivery scaffold (DDDS) loaded with Chinese herbs significantly increased the regenerated bone volume fraction. This study aimed to confirm the synergistic anti-inflammatory and osteogenic preclinical effects of this system.Methods: The targets and pathways of parthenolide and naringin were predicted. Three cell models were used to assess the anti-inflammatory effects of parthenolide and the osteogenic effects of naringin. First, the distance between the cementoenamel junction and alveolar bone crest (CEJ-ABC) and the bone mineral density (BMD) of surgical defects were measured in a rat model of periodontitis with periodontal fenestration defects. Additionally, the mRNA expression levels of matrix metallopeptidase 9 (MMP9) and alkaline phosphatase (ALP) were measured. Furthermore, the number of inflammatory cells and osteoclasts, as well as the protein expression levels of tumor necrosis factor-alpha (TNF-a) and levels of ALP were determined. Results: Target prediction suggested prostaglandin peroxidase synthase (PTGS2) as a potential target of parthenolide, while cytochrome P450 family 19 subfamily A1 (CYP19A1) and taste 2 receptor member 31 (TAS2R31) were potential targets of naringin. Parthenolide mainly targeted inflammation-related pathways, while naringin participated in steroid hormone synthesis and taste transduction. In vitro experiments revealed significant anti-inflammatory effects of parthenolide on RAW264.7 cells, and significant osteogenic effects of naringin on bone marrow mesenchymal stem cells and MC3T3-E1 cells. DDDS loaded with parthenolide and naringin decreased the CEJ-ABC distance and increased BMD and ALP levels in a time-dependent manner. Inflammation was significantly alleviated after 14 days of DDDS treatment. Additionally, after 56 days, the DDDS group exhibited the highest BMD and ALP levels.Conclusions: DDDS loaded with parthenolide and naringin in a rat model achieved significant synergistic anti-inflammatory and osteogenic effects, providing powerful preclinical evidence.
引用
收藏
页码:20 / 37
页数:18
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