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ORIGINAL RESEARCH article

Front. Microbiol.
Sec. Antimicrobials, Resistance and Chemotherapy
Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1531258

Mesalazine: A Novel Therapeutic Agent for Periodontitis via Regulating Periodontal Microbiota and Inhibiting Porphyromonas gingivalis

Provisionally accepted
Wang Yuqi Wang Yuqi 1,2Ma Jun Ma Jun 2Wang Haoyu Wang Haoyu 1,2Yi Jingzheng Yi Jingzheng 3Bai Yuxin Bai Yuxin 1,2Min Hu Min Hu 1,2*Yan Jiaqing Yan Jiaqing 1,2*
  • 1 Jilin University, Changchun, China
  • 2 Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, Hospital of Stomatology, Jilin University, Changchun, Hebei Province, China
  • 3 Western Dental Kids, Fresno, United States

The final, formatted version of the article will be published soon.

    Introduction: Periodontitis and inflammatory bowel disease are chronic inflammatory diseases with shared epidemiological, biological, and therapeutic associations. Given the similarities in their pathogenic factors, this study hypothesized that mesalazine, a key treatment agent for inflammatory bowel disease, could also be effective in managing periodontitis.Methods: The antimicrobial effect of mesalazine on P. gingivalis was investigated in vitro, including observations of morphological changes on the surface of P. gingivalis. Additionally, the impact of mesalazine on both the formation and established plaque biofilms was examined. The antimicrobial mechanism was elucidated by assessing the expression of P. gingivalis virulence genes and determining the destructive effect of P. gingivalis cell membranes. An in vivo rat model of periodontitis was constructed to evaluate mesalazine's efficacy and its influence on the periodontal bacterial flora in the context of periodontitis.Results and discussion: Our results demonstrated that mesalazine concentrations ranging from 0.5 to 2 mg/mL significantly inhibited P. gingivalis proliferation over 72 hours. Flow cytometry revealed a marked reduction in the number of viable cells following mesalazine treatment. At the nanometer scale, mesalazine induced crumpling and rupture of the P. gingivalis surface, compromising cell membrane integrity. Mesalazine not only suppressed the formation of plaque biofilms by P. gingivalis and polymicrobial communities but also disrupted pre-existing biofilms. The data also suggested that mesalazine could disrupt the integrity of the P. gingivalis cell membrane and inhibit the expression of virulence factors. An animal model of periodontitis in rats was successfully constructed in vivo. Mesalazine treatment inhibited alveolar bone resorption, alleviated inflammation of periodontal tissues, and improved the composition of the periodontal flora to a healthier state. This study establishes that mesalazine can treat periodontitis through modulation of the periodontal flora, in addition to its antiinflammatory properties, thus broadening its classical therapeutic applications.

    Keywords: Periodontitis, Mesalazine, Porphyromonas gingivalis, Plaque biofilm, inflammatory bowel disease

    Received: 20 Nov 2024; Accepted: 06 Jan 2025.

    Copyright: © 2025 Yuqi, Jun, Haoyu, Jingzheng, Yuxin, Hu and Jiaqing. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Min Hu, Jilin University, Changchun, China
    Yan Jiaqing, Jilin University, Changchun, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.