Department of Medical, Oral and Biotechnological Science, University G.d'Annunzio, Chieti-Pescara, Italy.
Department of Innovative Technologies in Medicine and Dentistry, University G.d'Annunzio, Chieti-Pescara, Italy.
Mediators Inflamm. 2021 May 4;2021:5562340. doi: 10.1155/2021/5562340. eCollection 2021.
Inflammatory responses have been associated with delayed oral mucosal wound healing and the pathogenesis of the periodontal disease. The invasion of microbes into the tissues and the establishment of a chronic infection may be due to impaired healing. The protracted inflammatory phase may delay wound healing and probably support tissue fibrosis and reduce tissue regeneration. Vanillin is a well-known natural compound with potential anti-inflammatory capacity. Hence, we hypothesized that Vanillin could accelerate wound healing reducing inflammation and especially cytokine production making the oral tissue repair process easier.
Our hypothesis was tested using primary human gingival fibroblast (HGF) cell pretreated with Vanillin and primed with IL-1, as inductor of proinflammatory environment. After 24 hours of treatments, the gene expression and production of IL-6, TNF-, IL-8, COX-2, iNOS, and nitric oxide (NO) generation and the wound healing rate were determined.
In IL-1-primed cells, preincubation with Vanillin reduced IL-6, IL-8, COX-2, and iNOS expression and NO release, compared to IL-1-primed cells. Moreover, Vanillin determines the increased gene expression of nAChR7, leading us to hypothesize a role of Vanillin in the activation of the cholinergic anti-inflammatory pathway. Furthermore, in presence of mechanical injury, the Vanillin preincubation, wound closure may be reducing the expression and release of IL-6 and TNF- and upregulation of COX-2 and IL-8.
Together, the results of this study highlight the anti-inflammatory and tissue repair ability of Vanillin in IL-1-primed HGF. Therefore, Vanillin shows a potential therapeutic interest as an inflammatory modulator molecule with novel application in periodontal regeneration and oral health.
炎症反应与口腔黏膜延迟愈合和牙周病的发病机制有关。微生物侵入组织并建立慢性感染可能是由于愈合受损。延长的炎症期可能会延迟伤口愈合,并可能支持组织纤维化,减少组织再生。香草醛是一种具有潜在抗炎能力的知名天然化合物。因此,我们假设香草醛可以通过减少炎症和特别是细胞因子的产生来加速伤口愈合,使口腔组织修复过程更容易。
我们使用经香草醛预处理并经 IL-1 预刺激的原代人牙龈成纤维细胞(HGF)作为诱导炎症环境的诱导剂来检验我们的假设。治疗 24 小时后,测定基因表达和 IL-6、TNF-、IL-8、COX-2、iNOS 的产生以及伤口愈合率。
在 IL-1 预刺激的细胞中,与 IL-1 预刺激的细胞相比,香草醛预孵育可降低 IL-6、IL-8、COX-2 和 iNOS 的表达和 NO 的释放。此外,香草醛决定了 nAChR7 的基因表达增加,这使我们假设香草醛在胆碱能抗炎途径的激活中起作用。此外,在存在机械损伤的情况下,香草醛预孵育可能会降低 IL-6 和 TNF-α的表达和释放,并上调 COX-2 和 IL-8。
综上所述,本研究的结果强调了香草醛在 IL-1 预刺激的 HGF 中的抗炎和组织修复能力。因此,香草醛作为一种具有新型牙周再生和口腔健康应用潜力的炎症调节分子,具有潜在的治疗意义。