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10.1371/journal.pone.0183506

http://scihub22266oqcxt.onion/10.1371/journal.pone.0183506
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C5573680!5573680!28847008
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suck abstract from ncbi


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pmid28847008      PLoS+One 2017 ; 12 (8): ä
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  • Effects of metformin on inflammation, oxidative stress, and bone loss in a rat model of periodontitis #MMPMID28847008
  • de Araújo AA; Pereira Ade SBF; de Medeiros CACX; Brito GAde C; Leităo RFde C; Araújo Lde S; Guedes PMM; Hiyari S; Pirih FQ; de Araújo Júnior RF
  • PLoS One 2017[]; 12 (8): ä PMID28847008show ga
  • Aim: To evaluate the effects of metformin (Met) on inflammation, oxidative stress, and bone loss in a rat model of ligature-induced periodontitis. Materials & methods: Male albino Wistar rats were divided randomly into five groups of twenty-one rats each, and given the following treatments for 10 days: (1) no ligature + water, (2) ligature + water, (3) ligature + 50 mg/kg Met, (4) ligature + 100 mg/kg Met, and (5) ligature + 200 mg/kg Met. Water or Met was administered orally. Maxillae were fixed and scanned using Micro-computed Tomography (?CT) to quantitate linear and bone volume/tissue volume (BV/TV) volumetric bone loss. Histopathological characteristics were assessed through immunohistochemical staining for MMP-9, COX-2, the RANKL/RANK/OPG pathway, SOD-1, and GPx-1. Additionally, confocal microscopy was used to analyze osteocalcin fluorescence. UV-VIS analysis was used to examine the levels of malondialdehyde, glutathione, IL-1? and TNF-? from gingival tissues. Quantitative RT-PCR reaction was used to gene expression of AMPK, NF-?B (p65), and Hmgb1 from gingival tissues. Significance among groups were analysed using a one-way ANOVA. A p-value of p<0.05 indicated a significant difference. Results: Treatment with 50 mg/kg Met significantly reduced concentrations of malondialdehyde, IL-1?, and TNF-? (p < 0.05). Additionally, weak staining was observed for COX-2, MMP-9, RANK, RANKL, SOD-1, and GPx-1 after 50 mg/kg Met. OPG and Osteocalcin showed strong staining in the same group. Radiographically, linear measurements showed a statistically significant reduction in bone loss after 50 mg/kg Met compared to the ligature and Met 200 mg/kg groups. The same pattern was observed volumetrically in BV/TV and decreased osteoclast number (p<0.05). RT-PCR showed increased AMPK expression and decreased expression of NF-?B (p65) and HMGB1 after 50 mg/kg Met. Conclusions: Metformin, at a concentration of 50 mg/kg, decreases the inflammatory response, oxidative stress and bone loss in ligature-induced periodontitis in rats.
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