AI Article Synopsis

  • Periodontitis is a serious complication for diabetic patients, as it worsens their overall health and can create a cycle of worsening diabetes and gum disease.
  • A study on rats tested the effects of the GLP-1 receptor agonist liraglutide, which was found to reduce inflammation and help improve periodontitis symptoms by decreasing certain inflammatory cells.
  • Liraglutide not only helped lower glucose levels but also showed potential benefits in treating periodontitis by reducing bone loss and inflammatory markers associated with the disease.

Article Abstract

Periodontitis is one of the diabetic complications due to its high morbidity and severity in patients with diabetes. The prevention of periodontitis is especially important in diabetic patients because the relationship between diabetes and periodontitis is bidirectional. Here, we evaluated the impacts of glucagon-like peptide-1 (GLP-1) receptor agonist liraglutide on the amelioration of periodontitis. Five-wk-old Male Sprague-Dawley (SD) rats ( = 30) were divided into 3 groups: normal, periodontitis, and periodontitis with liraglutide treatment groups. Periodontitis was induced by ligature around the maxillary second molar in SD rats. Half of the rats were administered liraglutide for 2 weeks. Periodontitis was evaluated by histological staining, gene expressions of inflammatory cytokines in gingiva, and microcomputed tomography. Periodontitis increased inflammatory cell infiltration, macrophage accumulation, and gene expressions of tumor necrosis factor- and inducible nitric oxide synthase in the gingiva, all of which were ameliorated by liraglutide. Liraglutide decreased M1 macrophages but did not affect M2 macrophages in periodontitis. Moreover, ligature-induced alveolar bone resorption was ameliorated by liraglutide. Liraglutide treatment also reduced osteoclasts on the alveolar bone surface. These results highlight the beyond glucose-lowering effects of liraglutide on the treatment of periodontitis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695495PMC
http://dx.doi.org/10.1155/2020/8843310DOI Listing

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