Morphometric and histopathological evaluation of the effect of grape seed proanthocyanidin on alveolar bone loss in experimental diabetes and periodontitis
Autor: | Fikret Gevrek, Hulya Toker, H. Balci Yuce, A. Lektemur Alpan, Mahfuz Elmastas |
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Přispěvatelé: | [Toker, H. -- Alpan, A. Lektemur] Cumhuriyet Univ, Dept Periodontol, Fac Dent, Sivas, Turkey -- [Yuce, H. Balci] Gaziosmanpasa Univ, Dept Periodontol, Fac Dent, Tokat, Turkey -- [Gevrek, F.] Gaziosmanpasa Univ, Dept Histol & Embryol, Fac Med, Tokat, Turkey -- [Elmastas, M.] Gaziosmanpasa Univ, Fac Arts & Sci, Dept Chem, Tokat, Turkey, balci yuce, hatice -- 0000-0003-3574-9751, LEKTEMUR ALPAN, AYSAN -- 0000-0002-5939-4783 |
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Blood Glucose
Male Vascular Endothelial Growth Factor A 0301 basic medicine alveolar bone loss medicine.medical_treatment Alveolar Bone Loss Osteoclasts Antioxidants chemistry.chemical_compound 0302 clinical medicine periodontitis diabetes Osteoblast Immunohistochemistry Vascular endothelial growth factor Matrix Metalloproteinase 8 medicine.anatomical_structure Periodontics Hypoxia-Inducible Factor 1 Injections Intraperitoneal medicine.drug medicine.medical_specialty Intraperitoneal injection Streptozocin Diabetes Mellitus Experimental 03 medical and health sciences Osteoclast Internal medicine Diabetes mellitus Alveolar Process medicine Animals Proanthocyanidins Rats Wistar Periodontitis Ligation Dental alveolus Inflammation Osteoblasts Grape Seed Extract Tartrate-Resistant Acid Phosphatase business.industry Body Weight 030206 dentistry Streptozotocin medicine.disease Rats Disease Models Animal 030104 developmental biology Endocrinology chemistry grape seed proanthocyanidins tartrate-resistant acid phosphatase business |
Popis: | WOS: 000432018000022 PubMed ID: 29446089 Objective: Grape seed proanthocyanidine extract (GSPE) is a strong antioxidant derived from the grape seeds (Vitis vinifera, Terral J.F.) and has a polyphenolic structure with a wide range of biological activity. The aim of the present study was to evaluate the effects of GSPE on alveolar bone loss and histopathological changes in rats with diabetes mellitus and ligature-induced periodontitis. Material and Methods: Forty rats were divided into 6 study groups. Control (C, 6 rats) group, periodontitis (P, 6 rats) group, diabetes (D, 6 rats) group, diabetes and periodontitis (D+P, 6 rats) group, diabetes, periodontitis and 100 mg/kg/day GSPE (GSPE-100, 8 rats), and diabetes, periodontitis and 200 mg/kg/day GSPE (GSPE-200, 8 rats) group. Diabetes mellitus was induced by intraperitoneal injection of a single dose of streptozotocin (60 mg/kg). Periodontitis was induced via ligation method. Silk ligatures were placed at the mandibular right first molars. GSPE was administered by oral gavage. After 30 days, all rats were killed. Alveolar bone loss was measured morphometrically via a stereomicroscope. For histopathological analyses, Alizarin red staining, and matrix metalloproteinase (MMP)-8, vascular endothelial growth factor and hypoxia inducible factor (HIF)-1 alpha immunohistochemistry were performed. Tartrate-resistant acid phosphatase-positive osteoclast cells and relative total inflammatory cells were also determined. Results: The highest alveolar bone loss was observed in the D+P group (P < .05). GSP-200 group decreased alveolar bone loss (P < .05). The D+P group had the highest osteoclast counts, but the difference was not significant compared to the P, GSPE-100 and GSPE-200 groups (P > .05). The inflammation in the D+P group was also higher than the other groups (P < .05). The osteoblast numbers increased in the GSPE-100 and GSPE-200 groups compared to the P and D+P groups (P < .05). MMP-8 and HIF-1 levels were highest in the D+P group and GSPE significantly decreased these levels (P < .05). Conclusion: Within the limits of this animal study, it can be suggested that GSPE administration may decrease periodontal inflammation and alveolar bone loss via decreasing MMP-8 and HIF-1 alpha levels and increase osteoblastic activity in diabetic rats with experimental periodontitis. |
Databáze: | OpenAIRE |
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