Chen Rui, Wang Mengting, Qi Qiaoling, Tang Yanli, Guo Zhenzhao, Wu Shuai, Li Qiyan
Department of Stomatology, The First People's Hospital of Yunnan Province, Kunming, China.
The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
J Periodontal Implant Sci. 2023 Feb;53(1):20-37. doi: 10.5051/jpis.2105700285. Epub 2022 Jul 25.
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.
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-α) and levels of ALP were determined.
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. 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.
DDDS loaded with parthenolide and naringin in a rat model achieved significant synergistic anti-inflammatory and osteogenic effects, providing powerful preclinical evidence.
我们的前期研究表明,负载中药的三维双药递送支架(DDDS)显著增加了再生骨体积分数。本研究旨在证实该系统协同抗炎和成骨的临床前效果。
预测了小白菊内酯和柚皮苷的靶点及信号通路。使用三种细胞模型评估小白菊内酯的抗炎作用和柚皮苷的成骨作用。首先,在患有牙周开窗缺损的牙周炎大鼠模型中,测量牙骨质釉质界与牙槽嵴顶之间的距离(CEJ-ABC)以及手术缺损处的骨密度(BMD)。此外,测量基质金属蛋白酶9(MMP9)和碱性磷酸酶(ALP)的mRNA表达水平。进一步测定炎症细胞和破骨细胞的数量,以及肿瘤坏死因子-α(TNF-α)的蛋白表达水平和ALP水平。
靶点预测表明前列腺素过氧化物酶合酶(PTGS2)是小白菊内酯的潜在靶点,而细胞色素P450家族19亚家族A1(CYP19A1)和味觉2受体成员31(TAS2R31)是柚皮苷的潜在靶点。小白菊内酯主要靶向炎症相关信号通路,而柚皮苷参与类固醇激素合成和味觉转导。实验揭示了小白菊内酯对RAW264.7细胞具有显著的抗炎作用,柚皮苷对骨髓间充质干细胞和MC3T3-E1细胞具有显著的成骨作用。负载小白菊内酯和柚皮苷的DDDS以时间依赖性方式减小了CEJ-ABC距离,并增加了BMD和ALP水平。DDDS治疗14天后炎症明显减轻。此外,56天后,DDDS组的BMD和ALP水平最高。
在大鼠模型中,负载小白菊内酯和柚皮苷的DDDS实现了显著的协同抗炎和成骨作用,提供了有力的临床前证据。