{"title":"Alyssin Modulates Inflammatory Mediators Expression in Interleukin-1β-Stimulated Human Periodontal Ligament Cells","authors":"Ikuko Hosokawa, Yoshitaka Hosokawa, Risa Okamoto, Kazumi Ozaki, Keiichi Hosaka","doi":"10.1002/jbt.70314","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Alyssin is an isothiocyanate found in cruciferous plants. It has been reported to have physiologically active effects. However, no attempts have been made to use alyssin for the treatment of periodontitis. In addition, there are no reports investigating the effects of alyssin on periodontal tissue constituent cells. In the present study, experiments were carried out to determine whether alyssin has an anti-inflammatory effect on human periodontal ligament cells (HPDLCs). We found that alyssin suppressed the interleukin (IL)-1β-induced production of IL-6, IL-8, C−C motif chemokine ligand (CCL)2, CCL20, and C−X−C motif chemokine ligand (CXCL)10 and the expression of intercellular adhesion molecule (ICAM)-1 and cyclooxygenase (COX)-2 in HPDLCs. It was also found that alyssin inhibited the IL-1β-induced activation of nuclear factor (NF)-κB and the phosphorylation of p70S6 kinase (p70S6K) in HPDLCs. Furthermore, we found that the expression of the antioxidant enzymes hemeoxygenase (HO)-1 and NAD(P)H:quinone oxidoreductase (NQO)-1 was enhanced by alyssin treatment of HPDLC. This study suggests that by suppressing the activation of NF-κB and p70S6K, alyssin may attenuate the expression of inflammatory mediators in HPDLCs. In addition, alyssin also increased the expression of antioxidant enzymes.</p></div>","PeriodicalId":15151,"journal":{"name":"Journal of Biochemical and Molecular Toxicology","volume":"39 6","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biochemical and Molecular Toxicology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jbt.70314","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Alyssin is an isothiocyanate found in cruciferous plants. It has been reported to have physiologically active effects. However, no attempts have been made to use alyssin for the treatment of periodontitis. In addition, there are no reports investigating the effects of alyssin on periodontal tissue constituent cells. In the present study, experiments were carried out to determine whether alyssin has an anti-inflammatory effect on human periodontal ligament cells (HPDLCs). We found that alyssin suppressed the interleukin (IL)-1β-induced production of IL-6, IL-8, C−C motif chemokine ligand (CCL)2, CCL20, and C−X−C motif chemokine ligand (CXCL)10 and the expression of intercellular adhesion molecule (ICAM)-1 and cyclooxygenase (COX)-2 in HPDLCs. It was also found that alyssin inhibited the IL-1β-induced activation of nuclear factor (NF)-κB and the phosphorylation of p70S6 kinase (p70S6K) in HPDLCs. Furthermore, we found that the expression of the antioxidant enzymes hemeoxygenase (HO)-1 and NAD(P)H:quinone oxidoreductase (NQO)-1 was enhanced by alyssin treatment of HPDLC. This study suggests that by suppressing the activation of NF-κB and p70S6K, alyssin may attenuate the expression of inflammatory mediators in HPDLCs. In addition, alyssin also increased the expression of antioxidant enzymes.
期刊介绍:
The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.