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羌活醇抑制牙周组织中的 NF-κB 通路并激活 PI3K/Akt/Nrf2 通路。

Notopterol Inhibits the NF-κB Pathway and Activates the PI3K/Akt/Nrf2 Pathway in Periodontal Tissue.

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Periodontics, West China Hospital of Stomatology, Med-X Center for Materials, Sichuan University, Chengdu, China.

出版信息

J Immunol. 2023 Nov 15;211(10):1516-1525. doi: 10.4049/jimmunol.2200727.

Abstract

Notopterol, an active component isolated from the traditional Chinese medicine Notopterygium incisum Ting ex H.T. Chang, exerts anti-inflammatory activity in rheumatoid arthritis. However, its roles in suppression of inflammatory insults and halting progression of tissue destruction in periodontitis remain elusive. In this study, we reveal that notopterol can inhibit osteoclastogenesis, thereby limiting alveolar bone loss in vivo. In vitro results demonstrated that notopterol administration inhibited synthesis of inflammatory mediators such as IL-1β, IL-32, and IL-8 in LPS-stimulated human gingival fibroblasts. Mechanistically, notopterol inhibits activation of the NF-κB signaling pathway, which is considered a prototypical proinflammatory signaling pathway. RNA sequencing data revealed that notopterol activates the PI3K/protein kinase B (Akt)/NF-E2-related factor 2 (Nrf2) signaling pathway in LPS-stimulated human gingival fibroblasts, a phenomenon validated via Western blot assay. Additionally, notopterol treatment suppressed reactive oxygen species levels by upregulating the expression of antioxidant genes, including heme oxygenase 1 (HO-1), NAD(P)H quinone oxidoreductase 1 (NQO1), catalase (CAT), and glutathione reductase (GSR), indicating that notopterol confers protection against oxidative stress. Notably, inhibition of Akt activity by the potent inhibitor, MK-2206, partially attenuated both anti-inflammatory and antioxidant effects of notopterol. Collectively, these results raise the possibility that notopterol relieves periodontal inflammation by suppressing and activating the NF-κB and PI3K/AKT/Nrf2 signaling pathways in periodontal tissue, respectively, suggesting its potential as an efficacious treatment therapy for periodontitis.

摘要

羌活醇是从传统中药羌活中分离得到的一种活性成分,具有抗炎活性,可用于治疗类风湿性关节炎。然而,其在抑制牙周炎炎症损伤和阻止组织破坏进展方面的作用仍不清楚。在这项研究中,我们揭示了羌活醇可以抑制破骨细胞的形成,从而限制体内牙槽骨的丢失。体外研究结果表明,羌活醇可抑制 LPS 刺激的人牙龈成纤维细胞中炎症介质如 IL-1β、IL-32 和 IL-8 的合成。在机制上,羌活醇抑制 NF-κB 信号通路的激活,该通路被认为是一种典型的促炎信号通路。RNA 测序数据显示,羌活醇在 LPS 刺激的人牙龈成纤维细胞中激活 PI3K/蛋白激酶 B(Akt)/核因子 E2 相关因子 2(Nrf2)信号通路,Western blot 实验验证了这一现象。此外,羌活醇通过上调抗氧化基因的表达来抑制活性氧水平,包括血红素加氧酶 1(HO-1)、NAD(P)H 醌氧化还原酶 1(NQO1)、过氧化氢酶(CAT)和谷胱甘肽还原酶(GSR),表明羌活醇对氧化应激具有保护作用。值得注意的是,通过强效抑制剂 MK-2206 抑制 Akt 活性,部分减弱了羌活醇的抗炎和抗氧化作用。综上所述,这些结果表明,羌活醇通过抑制和激活牙周组织中的 NF-κB 和 PI3K/Akt/Nrf2 信号通路,分别缓解牙周炎症,提示其在治疗牙周炎方面具有潜在的应用价值。

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