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Prophylactic supplement with melatonin successfully suppresses the pathogenesis of periodontitis through normalizing RANKL/OPG ratio and depressing the TLR4/MyD88 signaling pathway.
Renn, Ting-Yi; Huang, Yung-Kai; Feng, Sheng-Wei; Wang, Hsiao-Wei; Lee, Wei-Fang; Lin, Che-Tong; Burnouf, Thierry; Chen, Li-You; Kao, Pan-Fu; Chang, Hung-Ming.
Afiliação
  • Renn TY; Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
  • Huang YK; School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Feng SW; School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Wang HW; School of Dentistry - Master and PhD Program, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Lee WF; School of Dental Technology, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Lin CT; Department of Dentistry, Taipei Medical University Hospital, Taipei, Taiwan.
  • Burnouf T; Graduate Institute of Biomedical Materials and Tissue Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei, Taiwan.
  • Chen LY; International PhD Program in Biomedical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei, Taiwan.
  • Kao PF; Department of Anatomy, School of Medicine, College of Medicine, Chung Shan Medical University, Taichung, Taiwan.
  • Chang HM; Department of Nuclear Medicine, School of Medicine, College of Medicine, Chung Shan Medical University, Taichung, Taiwan.
J Pineal Res ; 64(3)2018 Apr.
Article em En | MEDLINE | ID: mdl-29274168
Periodontitis (PD) is an inflammatory disease characterized by gingival inflammation and resorption of alveolar bone. Impaired receptor activator of nuclear factor-kappa B ligand/osteoprotegerin (RANKL/OPG) signaling caused by enhanced production of pro-inflammatory cytokines plays an essential role in the pathogenesis of PD. Considering melatonin possesses significant anti-inflammatory property, this study aimed to determine whether prophylactic treatment with melatonin would effectively normalize RANKL/OPG signaling, depress toll-like receptor 4/myeloid differentiation factor 88 (TLR4/MyD88)-mediated pro-inflammatory cytokine activation, and successfully suppress the pathogenesis of PD. PD was induced in adult rats by placing the ligature at molar subgingival regions. Fourteen days before PD induction, 10, 50, or 100 mg/kg of melatonin was intraperitoneally injected for consecutive 28 days. Biochemical and enzyme-linked immunosorbent assay were used to detect TLR4/MyD88 activity, RANKL, OPG, interleukin 1ß, interleukin 6, and tumor necrosis factor-α levels, respectively. The extent of bone loss, bone mineral intensity, and calcium intensity was further evaluated by scanning electron microscopy, micro-computed tomography, and energy-dispersive X-ray spectroscopy. Results indicated that high RANKL/OPG ratio, TLR4/MyD88 activity, and pro-inflammatory cytokine levels were detected following PD. Impaired biochemical findings paralleled well with severe bone loss and reduced calcium intensity. However, in rats pretreated with melatonin, all above parameters were successfully returned to nearly normal levels with maximal change observed in rats receiving 100 mg/kg. As prophylactic treatment with melatonin effectively normalizes RANKL/OPG signaling by depressing TLR4/MyD88-mediated pro-inflammatory cytokine production, dietary supplement with melatonin may serve as an advanced strategy to strengthen oral health to counteract PD-induced destructive damage.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Periodontite / Transdução de Sinais / Melatonina / Antioxidantes Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Periodontite / Transdução de Sinais / Melatonina / Antioxidantes Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article