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1.
Niger J Clin Pract ; 24(7): 965-972, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34290170

ABSTRACT

BACKGROUND: IL-13 is the key cytokine in the regulation of inflammatory with an autoimmune disease and has an anti-inflammatory effect. AIMS: This study aimed to compare IL-13 (-1112 C/T and -1512 A/C) gene polymorphisms in patients with aggressive periodontitis (AgP), chronic periodontitis (CP), and periodontally healthy group (C) and evaluate the effect of nonsurgical periodontal therapy on gingival crevicular fluid (GCF) IL-13 levels in patients. MATERIALS AND METHODS: One hundred thirty patients with AgP, 120 patients with CP, and 70 periodontally healthy subjects were included in this study. Clinical parameters were recorded (plaque and gingival index, probing pocket depth, clinical attachment level), and GCF and blood samples were taken at baseline and 6-week. Nonsurgical periodontal therapy was performed in patients with periodontitis. Gene analyses (IL-13 - 1112C/T (rs1800925) and - 1512 A/C (rs1881457) were performed with real-time polymerase chain reaction (PCR) and cytokine levels were determined by an enzyme-linked immunosorbent assay method. RESULTS: AgP and CP patients showed significant improvement in clinical parameters after periodontal therapy (P < 0.05). According to results, genotype distributions and allele frequencies in IL-13 variants - 1112C/T and - 1512 A/C were found similarly in all groups (P > 0.05). In the AgP group, GCF IL-13 cytokine level is statistically significant and increased in 6 weeks; however, in the CP group, there is no statistically significant difference between baseline and 6 week. In the AgP group, baseline GCF IL-13 cytokine level is lower than those of the CP group and C group (P < 0.05). CONCLUSION: Within the limits of this study, IL-13 -1112 and -1512 gene polymorphisms have not been associated with AgP and CP, and GCF IL-13 cytokine level is increased after treatment in the AgP group.


Subject(s)
Aggressive Periodontitis , Chronic Periodontitis , Aggressive Periodontitis/genetics , Aggressive Periodontitis/therapy , Chronic Periodontitis/genetics , Chronic Periodontitis/therapy , Gingival Crevicular Fluid , Humans , Interleukin-13/genetics , Polymorphism, Genetic
2.
J Periodontal Res ; 53(3): 478-486, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29446089

ABSTRACT

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)-1α 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-1α 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-1α levels and increase osteoblastic activity in diabetic rats with experimental periodontitis.


Subject(s)
Alveolar Bone Loss/drug therapy , Alveolar Bone Loss/pathology , Diabetes Mellitus, Experimental/complications , Grape Seed Extract/pharmacology , Grape Seed Extract/therapeutic use , Periodontitis/drug therapy , Periodontitis/pathology , Proanthocyanidins/pharmacology , Proanthocyanidins/therapeutic use , Alveolar Bone Loss/classification , Alveolar Process/pathology , Animals , Antioxidants/pharmacology , Antioxidants/therapeutic use , Blood Glucose/analysis , Body Weight , Disease Models, Animal , Grape Seed Extract/administration & dosage , Hypoxia-Inducible Factor 1/analysis , Immunohistochemistry , Inflammation/drug therapy , Inflammation/pathology , Injections, Intraperitoneal , Ligation/adverse effects , Male , Matrix Metalloproteinase 8/analysis , Osteoblasts/drug effects , Osteoblasts/pathology , Osteoclasts/drug effects , Osteoclasts/pathology , Proanthocyanidins/administration & dosage , Rats , Rats, Wistar , Streptozocin/administration & dosage , Streptozocin/pharmacology , Tartrate-Resistant Acid Phosphatase/analysis , Vascular Endothelial Growth Factor A/analysis
3.
J Periodontal Res ; 53(1): 131-138, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29044575

ABSTRACT

BACKGROUND AND OBJECTIVE: Astaxanthin is a keto-carotenoid that has a strong antioxidant effect. The purpose of this study was to evaluate the effects of astaxanthin on alveolar bone loss and histopathological changes in ligature-induced periodontitis in rats. MATERIAL AND METHODS: Wistar rats were divided into four experimental groups: non-ligated (C, n = 6); ligature only (L, n = 6); ligature and astaxanthin (1 mg/kg/day astaxanthin, AS1 group, n = 8); ligature and astaxanthin (5 mg/kg/day astaxanthin, AS5 group, n = 8). Silk ligatures were placed at the gingival margin of lower first molars of the mandibular quadrant. The study duration was 11 days and the animals were killed at the end of this period. Changes in alveolar bone levels were clinically measured and tissues were immunohistochemically examined, osteocalcin, bone morphogenic protein-2, inducible nitric oxide synthase, Bax and bcl-2 levels in alveolar bone and tartrate-resistant acid phosphatase-positive osteoclast cells, osteoblast and inflammatory cell counts were determined. RESULTS: Alveolar bone loss was highest in the L group and the differences among the L, AS1 and AS5 groups were also significant (P < .05). Both doses of astaxanthin decreased tartrate-resistant acid phosphatase-positive+ osteoclast cell and increased osteoblast cell counts (P < .05). The inflammation in the L group was also higher than those of the C and AS1 groups were (P < .05) indicating the anti-inflammatory effect of astaxanthin. Although inducible nitric oxide synthase, osteocalcin, bone morphogenic protein-2 and bax staining percentages were all highest in the AS5 group and bcl-2 staining percentage was highest in the AS1 group, values were close to each other (P > .05). CONCLUSION: Within the limits of this study, it can be suggested that astaxanthin administration may reduce alveolar bone loss by increasing osteoblastic activity and decrease osteoclastic activity in experimental periodontitis model.


Subject(s)
Alveolar Bone Loss/prevention & control , Antioxidants/pharmacology , Periodontitis/drug therapy , Animals , Bone Morphogenetic Protein 2/metabolism , Cell Count , Disease Models, Animal , Nitric Oxide Synthase/metabolism , Osteoblasts/drug effects , Osteocalcin/metabolism , Rats, Wistar , Xanthophylls/pharmacology , bcl-2-Associated X Protein/metabolism
4.
Aust Dent J ; 61(1): 71-75, 2016 Mar.
Article in English | MEDLINE | ID: mdl-25892582

ABSTRACT

BACKGROUND: Evidence has suggested that males and females experience and report feeling pain differently. The aim of this study was to determine the postoperative perception levels of both females and males after neodymium-doped yttrium aluminum garnet (Nd:YAG) laser frenectomy and conventional frenectomy, and to compare the perceptions between genders. METHODS: Eighty-nine patients requiring frenectomy were randomly assigned to have treatment with either the conventional frenectomy or with the Nd:YAG laser. Postoperative discomfort (pain, chewing, talking) was recorded using a visual analog scale (VAS) on the operation day and postoperative days 1, 3, 7 and 10. RESULTS: According to the female VAS scores of the pain, chewing and speaking discomfort were statistically higher in the conventional group than those of the laser group on the operation day, and on the first and third postoperative days. Pain discomfort in males was statistically higher in the conventional group than those of the laser group on the operation day. Speaking discomfort in males was statistically higher in the conventional group than those of the laser group on the operation day and the first postoperative day. CONCLUSIONS: The present study indicated that Nd:YAG laser treatment used for frenectomies provides better postoperative comfort for each gender, especially in females in terms of pain, chewing and speaking than the conventional procedure up to the seventh postoperative day. According to our results, Nd:YAG laser may provide a safe, bloodless, painless surgery and an impressive alternative for frenectomy operations.

5.
Minerva Stomatol ; 63(4): 103-10, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24705040

ABSTRACT

AIM: Hydrogen sulphide (H2S), recently considered the third endogenous gaseous transmitter capable of modulating many physiological processes. The purpose of this study was to analyze the morphometric and histopathological changes associated with experimental periodontitis in rats in response to systemic administration of H2S METHODS: Forty-eight Wistar rats were divided into six experimental groups: non-ligated (NL) group; ligature only (LO) group; systemic administration of NaHS (H2S donor drug) alone (NaHS) group (14 µmol/kg body weight per day); and ligature placed and systemic administration of three different doses of NaHS groups (14, 28 and 70 µmol/kg/day) (L-NaHS-14, L-NaHS-28 and L-NaHS-70, respectively). Silk ligatures were placed at the gingival margin of lower first molars. Changes in alveolar bone levels were clinically measured and tissues were histopathologically examined. RESULTS: At the end of 15 days alveolar bone loss significantly higher in the entire ligature (LO and L-NaHS-14, -28 and -70) groups compared to the unligated groups (P<0.05) but there were no statistically significant differences in alveolar bone loss between LO and L-NaHS groups. Osteoclast number was significantly lower in L-NaHS-70 group than those of L-NaHS-14 and L-NaHS-28 groups (P<0.05). The osteoblastic activity of the L-NaHS-14 and -70 groups were significantly higher than those of the other groups (P<0.05). CONCLUSION: The findings of this study suggested that NaHS, when administered systemically with three different doses, did not prevent or increase alveolar bone loss in the rat model.


Subject(s)
Alveolar Bone Loss/etiology , Alveolar Process/drug effects , Alveolar Process/pathology , Hydrogen Sulfide/pharmacology , Periodontitis/complications , Animals , Male , Rats , Rats, Wistar
6.
J Periodontal Res ; 48(6): 722-6, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23452156

ABSTRACT

AIM: The purpose of this study was to analyze histologically the effect of ozone therapy in combination with autogenous bone graft on bone healing in rat calvaria. METHODS: Critical size defects were created in calvaria of 27 male Wistar rats. The animals were divided into three groups of nine animals each: autogenous bone graft group (n = 9); autogenous bone graft with ozone therapy group (80%, 30 s 3 d for 2 wk, n = 9); non-treatment (control) group (n = 9). Animals were killed after 8 wk. Histomorphometric assessments, using image analysis software, and histological analyses were performed. Primary outcome was total bone area. Secondary outcomes (osteoblast number, new bone formation) were also measured. RESULTS: Histomorphometrically, the total bone area in the autogenous bone graft with ozone therapy group (9.3 ± 2.2) were significantly higher than that of the autogenous bone graft group (5.1 ± 1.8) (p < 0.05). Also, the ozone therapy group significantly increased the percentage of total bone area compared to the autogenous bone graft group (p < 0.05). The osteoblast number significantly increased in the autogenous bone graft with the ozone therapy group (58 ± 12.3) compared to the autogenous bone graft group (9.3 ± 3.5) (p < 0.05). Also, it was observed that autogenous bone graft with ozone therapy group showed significant new bone formation when compared to the autogenous bone graft group (p < 0.05). CONCLUSION: Ozone therapy enhances new bone formation by autogenous bone graft in the rat calvarial defect model.


Subject(s)
Autografts/transplantation , Bone Diseases/surgery , Bone Transplantation , Ozone/therapeutic use , Skull/surgery , Animals , Autografts/drug effects , Autografts/pathology , Blood Vessels/pathology , Bone Diseases/pathology , Cell Count , Collagen , Connective Tissue/pathology , Fibroblasts/pathology , Image Processing, Computer-Assisted/methods , Male , Osteoblasts/drug effects , Osteoblasts/pathology , Osteogenesis/drug effects , Photography/methods , Rats , Rats, Wistar , Skull/drug effects , Skull/pathology , Time Factors , Wound Healing/drug effects
7.
J Periodontal Res ; 47(6): 793-9, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22712627

ABSTRACT

BACKGROUND AND OBJECTIVE: The purpose of this study was to evaluate the morphometric and histopathological changes associated with experimental periodontitis in diabetic rats in response to systemic administration of N-acetylcysteine (NAC), a sulfhydryl-containing thiol antioxidant. MATERIAL AND METHODS: Sixty Wistar rats were divided into six experimental groups: nonligated (NL) group; ligature-only (L) group; streptozotocin-only (STZ) group; STZ and ligature (STZ + L) group; and systemic administration of NAC and ligature (70 and 100 mg/kg body weight per day, respectively) (NAC70 and NAC100 groups). Diabetes mellitus was induced by 60 mg/kg of streptozotocin. Silk ligatures were placed at the gingival margin of the lower first molars of the mandibular quadrant. The study duration was 30 d and the animals were killed at the end of this period. Changes in alveolar bone levels were clinically measured and tissues were histopathologically examined to assess the differences among the study groups. RESULTS: At the end of the 30-d study period, alveolar bone loss was significantly higher in the STZ + L group compared with the other groups (p < 0.05). Also, alveolar bone loss in all the NAC groups was significantly lower than in the STZ + L and L groups (p < 0.05). The osteoblastic activity in the NAC100 group was significantly higher than in the other groups (p < 0.05). CONCLUSION: Within the limits of this study, it can be suggested that NAC, when administered systemically, prevents alveolar bone loss in the diabetic rat model.


Subject(s)
Acetylcysteine/therapeutic use , Alveolar Bone Loss/prevention & control , Antioxidants/therapeutic use , Diabetes Mellitus, Experimental/complications , Periodontitis/drug therapy , Alveolar Bone Loss/etiology , Animals , Diabetes Mellitus, Experimental/chemically induced , Osteoblasts/physiology , Periodontitis/complications , Rats , Rats, Wistar , Streptozocin
8.
Int J Dent Hyg ; 7(2): 115-20, 2009 May.
Article in English | MEDLINE | ID: mdl-19413547

ABSTRACT

OBJECTIVE: Gingival recession is a common manifestation of periodontal disease, but is also associated with several risk factors. In this study, we investigated prevalence of gingival recession and assessed various risk indicators in a university dental hospital in Turkey. MATERIALS AND METHODS: The study group consisted of 831 persons (537 females, 294 males). Gingival recession, dental plaque, calculus, tobacco consumption, toothbrushing frequency, traumatic toothbrushing and high frenum were assessed. Gingival recession scored as present whenever the free gingival margin was apical to the cemento-enamel junction and root surface was exposed. RESULTS: Overall, the prevalence of gingival recession was 78.2%. The gingival recession for buccal surfaces measured approximately between 1 and 2 mm was 17.4%. The number of gingival recession site of male subjects was significantly higher than that of the female ones (P < 0.05). The dental calculus and plaque levels of mandibular teeth were significantly higher than those of the maxillary teeth (P < 0.05). The multiple regression analyses showed that age, smoking duration, traumatic toothbrushing and high frenum are significant contributors to gingival recession. CONCLUSIONS: Periodontal condition is very high in this population. High level of gingival recession in this population is significantly associated with a high level of dental plaque and calculus, male gender, smoking duration, toothbrushing frequency, traumatic toothbrushing and high frenum.


Subject(s)
Gingival Recession/epidemiology , Adolescent , Adult , Aged , Dental Calculus/epidemiology , Dental Plaque/epidemiology , Dental Service, Hospital/statistics & numerical data , Epidemiologic Studies , Female , Gingiva/pathology , Humans , Labial Frenum/pathology , Male , Mandible/pathology , Maxilla/pathology , Middle Aged , Prevalence , Risk Factors , Sex Factors , Smoking/epidemiology , Tooth Cervix/pathology , Tooth Root/pathology , Toothbrushing/statistics & numerical data , Turkey/epidemiology , Young Adult
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