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Therapeutic Effects of Hinokitiol through Regulating the SIRT1/NOX4 against Ligature-Induced Experimental Periodontitis

机译:桧木酚通过调节 SIRT1/NOX4 对结扎诱导的实验性牙周炎的治疗作用

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摘要

Hinokitiol (HKT) is one of the essential oil components found in the heartwood of Cupressaceae plants, and has been reported to have various bioactive effects, including anti-inflammatory effects. However, the improving effect of HKT on periodontitis, which is characterized by periodontal tissue inflammation and alveolar bone loss, has not been clearly revealed. Therefore, we investigated the periodontitis-alleviating effect of HKT and the related molecular mechanisms in human periodontal ligament cells. According to the study results, HKT downregulated SIRT1 and NOX4, which were increased by Porphyromonas gingivalis Lipopolysaccharide (PG-LPS) stimulation and were found to regulate pro-inflammatory mediators and oxidative stress through SIRT1/NOX4 signals. Additionally, by increasing the expression of osteogenic makers such as alkaline phosphatase, osteogenic induction of human periodontal ligament (HPDL) cells, which had been reduced by PG-LPS, was restored. Furthermore, we confirmed that NOX4 expression was regulated through regulation of SIRT1 expression with HKT. The in vitro effect of HKT on improving periodontitis was proven using the periodontal inflammation model, which induces periodontal inflammation using ligature, a representative in vivo model. According to in vivo results, HKT alleviated periodontal inflammation and restored damaged alveolar bone in a concentration-dependent manner in the periodontal inflammation model. Through this experiment, the positive effects of HKT on relieving periodontal tissue inflammation and recovering damaged alveolar bone, which are important treatment strategies for periodontitis, were confirmed. Therefore, these results suggest that HKT has potential in the treatment of periodontitis.
机译:桧木酚 (HKT) 是在柏科植物心材中发现的精油成分之一,据报道具有多种生物活性作用,包括抗炎作用。然而,HKT 对牙周炎的改善作用尚未明确揭示,牙周炎的特点是牙周组织炎症和牙槽骨质流失。因此,我们研究了 HKT 的牙周炎缓解作用以及人牙周膜细胞中的相关分子机制。根据研究结果,HKT 下调了 SIRT1 和 NOX4,这些 SIRT和NOX4在牙龈卟啉单胞菌脂多糖(PG-LPS)刺激下调,并发现通过SIRT1/NOX4信号调节促炎介质和氧化应激。此外,通过增加碱性磷酸酶等成骨成分的表达,恢复了被 PG-LPS 减少的人牙周韧带 (HPDL) 细胞的成骨诱导。此外,我们证实 NOX4 表达是通过 HKT 调节 SIRT1 表达来调节的。HKT 对改善牙周炎的体外作用使用牙周炎模型得到证实,该模型使用具有代表性的体内模型结扎诱导牙周炎。根据体内结果,在牙周炎模型中,HKT 以浓度依赖性方式减轻牙周炎并恢复受损的牙槽骨。通过本实验,证实了 HKT 对缓解牙周组织炎症和恢复受损牙槽骨的积极作用,这是牙周炎的重要治疗策略。因此,这些结果表明 HKT 在治疗牙周炎方面具有潜力。

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