姜黄素通过抑制结扎诱导的牙周炎小鼠的铁死亡减轻牙周损伤。

Curcumin Attenuates Periodontal Injury via Inhibiting Ferroptosis of Ligature-Induced Periodontitis in Mice.

机构信息

Department of Periodontics, Affiliated Stomatology Hospital of Guangzhou Medical University, Guangdong Engineering Research Center of Oral Restoration and Reconstruction, Guangzhou Key Laboratory of Basic and Applied Research of Oral Regenerative Medicine, Guangzhou 510182, China.

Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, Hospital of Stomatology, Jilin University, Changchun 130021, China.

出版信息

Int J Mol Sci. 2023 Jun 7;24(12):9835. doi: 10.3390/ijms24129835.

Abstract

Periodontitis is a chronic infectious disease characterized by the destruction of connective tissue and alveolar bone that eventually leads to tooth loss. Ferroptosis is an iron-dependent regulated cell death and is involved in ligature-induced periodontitis in vivo. Studies have demonstrated that curcumin has a potential therapeutic effect on periodontitis, but the mechanism is still unclear. The purpose of this study was to investigate the protective effects of curcumin on alleviating ferroptosis in periodontitis. Ligature-induced periodontal-diseased mice were used to detect the protective effect of curcumin. The level of superoxide dismutase (SOD), malondialdehyde (MDA) and total glutathione (GSH) in gingiva and alveolar bone were assayed. Furthermore, the mRNA expression levels of , , and were measured using qPCR and the protein expression of ACSL4, SLC7A11, GPX4 and TfR1 were investigated by Western blot and immunocytochemistry (IHC). Curcumin reduced the level of MDA and increased the level of GSH. Additionally, curcumin was proven to significantly increase the expression levels of SLC7A11 and GPX4 and inhibit the expression of ACSL4 and TfR1. In conclusion, curcumin plays a protective role by inhibiting ferroptosis in ligature-induced periodontal-diseased mice.

摘要

牙周炎是一种慢性感染性疾病,其特征为结缔组织和牙槽骨的破坏,最终导致牙齿脱落。铁死亡是一种铁依赖性的细胞死亡方式,参与体内结扎诱导的牙周炎。研究表明姜黄素对牙周炎具有潜在的治疗作用,但机制尚不清楚。本研究旨在探讨姜黄素对缓解牙周炎中铁死亡的保护作用。采用结扎诱导牙周炎小鼠模型,检测姜黄素的保护作用。检测牙龈和牙槽骨中超氧化物歧化酶(SOD)、丙二醛(MDA)和总谷胱甘肽(GSH)的水平。此外,采用 qPCR 检测 、 、 和 的 mRNA 表达水平,采用 Western blot 和免疫细胞化学(IHC)检测 ACSL4、SLC7A11、GPX4 和 TfR1 的蛋白表达。姜黄素降低 MDA 水平,增加 GSH 水平。此外,姜黄素显著增加 SLC7A11 和 GPX4 的表达水平,并抑制 ACSL4 和 TfR1 的表达。综上所述,姜黄素通过抑制结扎诱导的牙周炎小鼠的铁死亡发挥保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4ec/10298010/26a9186019de/ijms-24-09835-g001.jpg

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