Melatonin improves periodontitis-induced kidney damages by decreasing inflammatory stress and apoptosis in rats

Background Two main aims of this animal study were to inspect the possible effects of periodontitis on the structure and functions of the kidneys and the therapeutic effectiveness of melatonin. Methods Twenty-four male Sprague-Dawley rats were randomly divided into three groups: control, experimenta...

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Veröffentlicht in:Journal of periodontology (1970) 2021-06, Vol.92 (6), p.22-34
Hauptverfasser: Kose, Oguz, Bayrakdar, Sevda Kurt, Unver, Busra, Altin, Ahmet, Akyildiz, Kerimali, Mercantepe, Tolga, Bostan, Semih Alperen, Arabaci, Taner, Sener, Leyla Turker, Kose, Taha Emre, Tumkaya, Levent, Yilmaz, Adnan, Kuluslu, Goker
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Sprache:eng
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Zusammenfassung:Background Two main aims of this animal study were to inspect the possible effects of periodontitis on the structure and functions of the kidneys and the therapeutic effectiveness of melatonin. Methods Twenty-four male Sprague-Dawley rats were randomly divided into three groups: control, experimental periodontitis (Ep), and Ep-melatonin (Ep-Mel). Periodontitis was induced by placing 3.0-silk sutures sub-paramarginally around the cervix of right-left mandibular first molars and maintaining the sutures for 5 weeks. Then melatonin (10 mg/kg body weight/day, 14 days), and the vehicle was administered intraperitonally. Mandibular and kidney tissue samples were obtained following the euthanasia. Periodontal bone loss was measured via histological and microcomputed tomographic slices. On right kidney histopathological and immunohistochemical, and on the left kidney biochemical (malonyl-aldehyde [MDA], glutathione, oxidative stress [OSI], tumor necrosis factor [TNF]-alpha, interleukin [IL]-1 beta, matrix metalloproteinase [MMP]-8, MMP-9, and cathepsin D levels) evaluations were performed. Renal functional status was analyzed by levels of serum creatinine, urea, cystatin-C, and urea creatinine. Results Melatonin significantly restricted ligature-induced periodontal bone loss (P
ISSN:0022-3492
1943-3670
DOI:10.1002/JPER.20-0434