Effects of erucin on inflammatory mediators and antioxidant enzymes' expression in TNF-α-stimulated human oral epithelial cells.

IF 2.9 4区 医学 Q3 IMMUNOLOGY Immunopharmacology and Immunotoxicology Pub Date : 2024-02-01 Epub Date: 2023-08-30 DOI:10.1080/08923973.2023.2250551
Masahiro Shimoyama, Yoshitaka Hosokawa, Ikuko Hosokawa, Kazumi Ozaki, Keiichi Hosaka
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Abstract

Objectives: Periodontitis is a chronic inflammatory disease induced by periodontal disease-causing bacteria. It has been shown that excessive immune response against bacteria is involved in periodontal tissue destruction including alveolar bone resorption. Erucin is a biologically active substance found in cruciferous plants such as arugula and is classified as an isothiocyanate. No previous studies have attempted to use erucin in the treatment of periodontitis, and there are no papers that have examined the effects of erucin on periodontal resident cells. The purpose of this study was to analyze the effects of erucin on the production of inflammatory and antioxidant mediators produced by tumor necrosis factor (TNF)-α-stimulated TR146 cells, an oral epithelial cell line, including its effects on signaling molecules.

Methods: Cytokine and chemokine levels were measured by ELISA. Protein expression in TR146 cells and activations of signal transduction pathway were determined by Western blotting.

Results: Our results indicate that erucin suppresses interleukin-6 and CXC-chemokine ligand 10 production and vascular cell adhesion molecule-1 expression in TNF-α-stimulated TR146 cells. In addition, erucin induced the production of the antioxidant enzymes, Heme Oxygenase-1 and NAD(P)H quinone dehydrogenase 1 in TR146 cells. Furthermore, erucin suppressed TNF-α-stimulated nuclear factor-κB, signal transducer and activator of transcription3, and phospho-70S6 Kinase-S6 ribosomal protein signaling pathways in TR146 cells. We have shown that erucin has anti-inflammatory effects on oral epithelial cells and also induces the production of antioxidant mediators.

Conclusions: These results suggest that erucin may provide a new anti-inflammatory agent that can be used in the treatment of periodontitis.

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麦角苷对 TNF-α 刺激的人口腔上皮细胞中炎症介质和抗氧化酶表达的影响
目的:牙周炎是一种由牙周致病菌诱发的慢性炎症性疾病。研究表明,针对细菌的过度免疫反应参与了牙周组织的破坏,包括牙槽骨吸收。芥酸苷是十字花科植物(如芝麻菜)中的一种生物活性物质,被归类为异硫氰酸盐。以前没有研究尝试使用芥子气苷治疗牙周炎,也没有论文研究芥子气苷对牙周驻留细胞的影响。本研究旨在分析麦角素对肿瘤坏死因子(TNF)-α刺激的口腔上皮细胞系TR146细胞产生的炎症和抗氧化介质的影响,包括对信号分子的影响:用酶联免疫吸附法测定细胞因子和趋化因子的水平。方法:用酶联免疫吸附法测定细胞因子和趋化因子的水平,用 Western 印迹法测定 TR146 细胞中蛋白质的表达和信号转导通路的激活情况:结果表明,麦角素能抑制TNF-α刺激的TR146细胞中白细胞介素-6和CXC-趋化因子配体10的产生以及血管细胞粘附分子-1的表达。此外,麦角素还能诱导 TR146 细胞产生抗氧化酶血红素加氧酶-1 和 NAD(P)H 醌脱氢酶 1。此外,麦角素还能抑制TNF-α刺激的核因子-κB、转录信号转导和激活因子3以及磷酸-70S6激酶-S6核糖体蛋白信号通路。我们的研究表明,麦角素对口腔上皮细胞具有抗炎作用,还能诱导产生抗氧化介质:这些结果表明,麦角素可能是一种新的抗炎剂,可用于治疗牙周炎。
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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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