Department of Oriental Medicinal Materials & Processing, College of Life Science, Kyung Hee University, Yongin-si, Gyeonggi-do, South Korea.
Mar Biotechnol (NY). 2018 Jun;20(3):313-323. doi: 10.1007/s10126-018-9814-8. Epub 2018 Apr 14.
The purpose of this study was to evaluate the effects of hiziki extract on alveolar bone loss, inflammation, and osteo-biomarker expression in hPDL cells (10, 50, 100 μg/ml final concentrations in culture medium) and on a ligature-induced periodontitis rat model (50, 100, 200 mg/kg with oral administration). Hiziki extract increased alkaline phosphatase activity and mineralized nodule formation in hPDL cell. In western blot analysis, hiziki extract resulted in increased expression of osteoblast markers, including transforming growth factor beta (TGF-β), SMAD anchor for receptor activation (SARA) and runt-related transcription factor 2 (RUNX2) in hDPL cells. Additionally, expression of osteoclast markers and inflammatory cytokines was inhibited, which were receptor activator of NF-κB (RANK), RANK receptor (RANKL) and nuclear factor of activated T cells, cytoplasmic 1 (NFATc1). Hiziki extract also prevented alveolar bone loss in a ligature-induced periodontitis rat model through reducing the distance between cementoenamel junction and alveolar bone crest (CBJ-ABC) and furcation involvement. These findings suggested that hiziki extract has prophylactic potential for the prevention of periodontitis through anti-inflammation and, anti-bone resorption effects and the inhibition of alveolar bone destruction.
本研究旨在评估藻褐素提取物对人牙周膜细胞(最终浓度为 10、50、100μg/ml 于培养基中)牙槽骨丢失、炎症和骨生物标志物表达的影响,以及对结扎诱导的牙周炎大鼠模型的影响(经口给予 50、100、200mg/kg)。藻褐素提取物增加了人牙周膜细胞的碱性磷酸酶活性和矿化结节形成。在 Western blot 分析中,藻褐素提取物导致成骨细胞标志物的表达增加,包括转化生长因子β(TGF-β)、SMAD 锚定受体激活(SARA)和 runt 相关转录因子 2(RUNX2)。此外,抑制了破骨细胞标志物和炎性细胞因子的表达,包括核因子κB 受体激活剂(RANK)、RANK 配体(RANKL)和激活 T 细胞的核因子,细胞质 1(NFATc1)。藻褐素提取物还通过减少牙骨质-牙槽骨交界(CBJ-ABC)和分叉受累之间的距离,预防结扎诱导的牙周炎大鼠模型中的牙槽骨丢失。这些发现表明,藻褐素提取物具有通过抗炎、抗骨吸收作用和抑制牙槽骨破坏来预防牙周炎的潜力。