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【Objective】 To analyze the expressions of IL-10, IL-35 and TGF-β in CD25+B cells from periodontitis individuals, and then establish how the activation of TLR4/9 affects the above processes. 【Methods】 SD rats were randomly divided into healthy group, primary periodontitis groups and severe periodontitis group; experimental models were performed by ligation. Expression of IL-10, IL-35 and TGF-β mRNA in CD25+B cells from gingiva and peripheral blood, expression and activation of TLR 2/4/7/9, MyD88, TRAF6 in gingival CD25+B cells were detected. The effect of TLRs/MyD88 on IL-10, IL-35 and TGF-β expressions and production were evaluated by cell culture experiments. 【Results】 CD25+B cells from gingiva of primary periodontitis individuals showed improved expression of IL-10 and TGF-β mRNA compared with the healthy ones (P<0.05); cells from peripheral blood did not present the same tendency. CD25+B cells from gingiva of severe periodontitis individuals showed improved expression of IL-10, IL-35 and TGF-β mRNA compared with the healthy ones (P<0.05), cells from peripheral blood showed higher IL-10 mRNA level than the healthy ones (P<0.05). Compared with healthy individuals, the expression and phosphorylation of TLR4/9 and MyD88 in CD25+B cells from gingiva of severe periodontitis individuals were increased (P<0.01). In cell culture experiments, TLR4 agonist promoted IL-10, IL-35 and TGF-β mRNA expression and IL-10 secretion (P<0.05); TLR9 agonist improved IL-10 and TGF-β mRNA expression and IL-10 secretion (P<0.05). The combined use of TLR4/9 agonist could increase the expression and secretion of all the detected indexes (P<0.05); MyD88 antagonism decrease the above effects (P<0.05). 【Conclusion】 The expressions of IL-10, IL-35 and TGF-β in gingiva CD25+B cells increase during periodontitis, which may be regulated by TLR4 /9-MyD88 pathway.
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Abstract Objective The purpose of this study is to investigate the pathogenic role of PPARα in periodontal antigen treated gingival cells in vitro and in experimental periodontitis in vivo . Methodology Gingival fibroblasts, gingival epithelial cells and splenocytes were isolated from C57BL/6J wild type (WT) mice and treated with fixed P. gingivalis at for 48 hours. The mRNA levels of PPARs, TNFα, IL-1β and IL-10 were detected by Real-time quantitative PCR. Silk ligatures after being soaked in the P.gingivalis suspension were tied around both maxillary second molars of WT mice or PPARα knock-out (KO) mice for two weeks. PPARα agonist fenofibrate and vehicle control were injected into the different side of the palatal gingiva on days 3, 6, and 9. At day 14, bone resorption and gingival mRNA expression levels of PPARs, TNFα, IL-1β and IL-10 were measured by micro-computed tomography and RT-qPCR respectively. Results P. gingivalis treatment downregulated the expression of PPARα, but not PPARβ or PPARγ, and increased the expression of TNF-α and IL-1β in Gingival fibroblasts, gingival epithelial cells and splenocytes from WT mice. Gingival mRNA levels of PPARα were significantly decreased in experimental periodontitis in WT mice. The bone loss of PPARα KO mice in experimental periodontitis was significantly higher than WT mice and was not reduced by fenofibrate treatment. Gingival TNFα protein expressions were significantly increased by P. gingivalis associated ligation and decreased by fenofibrate treatment in WT mice but not in PPARα KO mice. Conclusion This study suggests that PPARα plays an essential role in periodontitis.
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@#As the most important pathological feature of periodontitis, alveolar bone resorption also results in tooth loss and oral dysfunction. According to recent research, the host immune response is the major factor leading to alveolar bone resorption. Antibodies, immune cells and inflammatory cytokines involved in this procedure cause an imbalance of bone formation and destruction, which is called osteoimmunity. Given the importance of adaptive humoral immunity during periodontitis, B cells are considered crucial in the development of periodontitis. Therefore, establishing B cell osteoimmunity is an effective way for us to deeply assess the start, development and prognosis of periodontitis. It has been proven that the development process of B cells is accompanied by changes in bone density or morphology. We have reviewed previous literature to understand the role of B cell bone immunity in the pathological process of periodontitis, and the results showed that B cells regulate the development of bone cell lines through transcription factors (such as RANKL, PU.1, E2A, etc.). In addition, various cytokines expressed by B cells (such as IFN-γ, IL-17, IL-10, TGF-β, etc.) can participate in the regulation of bone cells.
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Objective To analyze the effect of astragalus polysacharin (APC) on bone resorption in experimental periodontitis, and evaluate its protective function of inflammatory resorption of alveolar bone in periodontits. Methods SD rats were randomly divided into five equal groups: contorol group, model group, and APC low [LD: 100 mg/(kg∙d)], medium [MD: 200 mg/(kg∙d)], and high dose [HD: 500 mg/(kg∙d)] treatment groups. The periodontitis models were established through Porphyromonas gingivalis attracting. APC [LD: 100 mg/(kg∙d); MD: 200 mg/(kg∙d); HD: 500 mg/(kg∙d)] gavage was given to treatment groups, and the same amount of normal saline was given to control and model groups. The rats executed after four weeks, their CEJ-ABC distance (CAD) and expression of IL-1β, IL-6, TNF-α, TOS, TAS, RANKL, OPG in their serum was evaluated, and the oxidative stress index (OSI) was calculated. Results As APC amount increased, CAD, TOS, and OSI levels were declined significantly; While TAS, RANKL, RANKL/OPG levels were improved significantly; There was no significantly change on IL-1β, IL-6, TNF-α, and OPG levesl among groups. Conclusion APC prevents alveolar bone from oxidative stress and inflammatory damage by down-regulating OSI and RANKL/OPG.
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Objetivo: avaliar via análises histológica, histométrica e imunoistoquímica, a influência do pH da droga fotossensibilizadora utilizada na aPDT para o tratamento da periodontite experimental (PE) induzida. Métodos: 120 animais foram divididos em 4 grupos: PE (n=30): recebeu indução da PE e não foi submetido a nenhum tratamento; RAR (n=30): recebeu indução da PE, e após 7 dias foi realizado tratamento de raspagem e alisamento radicular (RAR); aPDT -pH7 (n=30) recebeu indução da PE, e após 7 dias foi realizada RAR e terapia fotodinâmica antimicrobiana (aPDT) (660 nm; 0.035 W; 4,2 J; 120 s) empregando azul de metileno (AM) pH 7.0 como agente fotossensibilizador; aPDT-pH1 (n=30): recebeu indução da PE, e após 7 dias foi realizada RAR e aPDT (660 nm; 0.035 W; 4.2 J; 120 s) empregando AM pH 1.0 como agente fotossensibilizador. A PE foi induzida pela instalação de ligadura nos primeiros molares inferiores esquerdos de todos os animais, sendo removida aos 7 dias nos grupos tratados. Dez animais de cada grupo/período foram eutanasiados aos 7, 15 e 30 dias após tratamento. As peças coletadas foram submetidas a processamento histológico convencional, com desmineralização e inclusão em parafina. Secções semiseriadas de 4µm foram coradas com hematoxilina e eosina (HE) para as análises histológica e histométrica, ou processadas para imunomarcação de fosfatase ácida resistente ao tartarato (TRAP) e osteocalcina (OCN). Os dados foram analisados estatisticamente (p≤0,05). Resultados: maior porcentagem de osso na furca (POF) foi observada no grupo aPDT -pH1 (66,33%±7,35; 75,05%±2,66;78,4%±3,65)q uando comparado com todos os períodos dos grupos PE (27,09%±6,85; 31,33%±7,41; 29,67%±5,68) e RAR (58,61%±/10,46;57,03%±10,46; 63,24%±5,58)e, com 15 (68,48%±3,32)e 30 dias (72,96%±3,46) no grupo aPDT -pH7 (p≤O,05). A análise histológica mostrou maior severidade da doença periodontal no grupo PE, bem como características muito semelhantes entre grupos aPDT-pH7 e aPDT-pH1, ambos com menor processo inflamatório e progressão mais favorável do processo de reparo após tratamento quando comparados com o grupo RAR. Menor número de células TRAP-positivas foram observadas no grupo aPDT-pH1 (24,6±9,2; 22,4±10,6; 34±7,9 células) quando comparado com o grupo PE (41,8±5,80; 47,7±5,3; 63,5±10,5 células) e RAR (45,2±4,4; 52,2±9; 49,2±7,3 células) em todos os períodos, e no grupo aPDT-pH7 (31,4±5,68; 30,2±12,6; 26,4±7,9 células) quando comparado com os grupos PE aos 15 e 30 dias e RAR em todos os períodos (p≤0,05). Os grupos aPDT-pH7 e aPDT-pH1 apresentaram maior padrão de imunomarcação para OCN quando comparados com PE em todos os períodos e RAR aos 15 e 30 dias (p≤0,05). Conclusão: Assim, dentro dos limites do presente estudo, podemos concluir que o AM com pH 1.0 utilizado na aPDT, adjuvante à RAR, é seguro e efetivo para o tratamento da PE. Além do mais, o emprego do fotossensibilizador com Ph 1.0 se mostrou ainda mais eficaz no controle da perda óssea alveolar quando comparado ao AM com pH 7.0(AU)
The purpose of this study was to evaluate, through histologic, histometric and immunohistochemical analyzes, the influence ofthe pH of the photosensitizer agent used in antimicrobial photodynamic therapy (aPDT) for treatment of induced experimental periodontitis (EP). Methods: 120 Wistar rats were divided into 4 experimental groups: PE (n=30): EP was induced and no treatment was performed; SRP (n=30): EP was induced and, 7 days later, performed scaling and root planning (SRP); aPDT-pH7 (n=30): EP was induced and, 7 days later, performed SRP and aPDT (660 nm; 0.035 W; 4.2 J; 120 s) with methylene blue (MB) pH 7.0; aPDT-pH1 (n=30): EP was induced and, 7 days later, performed SRP and aPDT (660 nm; 0.035 W; 4.2 J; 120 s) with MB pH 1.0. EP was induced by the placement of a ligature in the left lower first molars of all animals. Ten animals per group/period were euthanized at 7, 15 and 30 days after treatment. The collected specimens underwent conventional histological processing with demineralization and paraffin embedding. Semi-serial 4 µm thickness sections were stained by hematoxylin and eosin (HE) for histologic and histometric analyses or immunohistochemically processed for detection of tartrate-resistant acid phosphatase (TRAP) and osteocalcin (OCN). The data were analyzed statistically (p≤0.05). Results: higher percentage of bone in the furcation (PBF) was observed in aPDT-pH1 (66.33%±7.35; 75.05%±2.66; 78.4%±3.65) when compared with all periods of groups EP (27.09%±6.85; 31.33%±7.41; 29.67%±5.68) and SRP( 58.61%±10.46; 57.03%±10.46; 63.24%±5.58), as well as with 15 (68.48%±3.32) and 30 days (72.96%±3.46) of aPDT-pH7 (p≤0.05). The histological analysis showed increased severity of the periodontal disease in group EP, as well as very similar histopathological characteristics between aPDT-pH7 and aPDT-pH1, both with lower inflammation and most favorable post treatment repair process when compared with group SRP. Smaller number of TRAP-positive cells was observed in aPDT-pH1 (24,6±9,2; 22,4±10,6; 34±7,9 cells) when compared with groups EP (41,8±5,80; 47,7±5,3; 63,5±10,5 cells) and SRP (45,2±4,4; 52,2±9; 49,2±7,3 cells) in all experimental periods, and in a aPDT-pH7 (31,4±5,68; 30,2±12,6; 26,4±7,9 cells) when compared with groups EP at 7 and 15 days and RAR in all experimental periods (p≤0,05). aPDT-pH7 and aPDT-pH1 showed higher OCN immunolabeling when compared with groups EP in all experimental periods and SRP at 15 and 30 days (p≤0,05). Conclusion: within the limits of the present study, we can conclude that MB with pH 1.0 used in a aPDT, adjuvant to SRP, is safe and effective for treatment of EP. Furthermore, the use of the photosensitizer pH 1.0 was more effective to control the alveolar bone loss when compared with MB with pH 7.0(AU)
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Animals , Rats , Methylene Blue , Periodontitis , PhotochemotherapyABSTRACT
Objective:To investigate the influence of type A behavior in the occurrence and development of chromic periodontitis and compare the differences among people with different behavior types in the occurrence and development of chronic periodontitis, and to explore the influence of psychological factors in the process of periodontitis.Methods:According the same standard,132 patients with periodontitis were selected as periodontitis group,and 126 patients without periodontitis were used as control group.OralSurveys Basic Methods proposed by WHO in 1987 and ReferenceStandard of Diagnosis and Treatment of Periodontitis made by AAP in 2000 were used to dignose the periodontitis.All subjects finished type A behavior and SCL-90 questionnaire (ZHANG Boyuan 1983,revision in 1985 ), their scores were recorded and the results were analyzed by t test. Results:The proportion of type A behavior in periodontits group (68.94%)was higher than that in control group (27.78%) (P<0.05)compared with type M and type B behavior.The scores of hostility (1.54±0.38),anxiety (1.47± 0.39),depression (1.41 ± 0.37),interpersonal sensitivity (1.23 ± 0.39),compulsive (1.72 ± 0.46),and somatizition (1.47 ± 0.38)were significantly higher than those in control group (1.32 ± 0.30, 1.29 ± 0.24, 1.25±0.23,1.04± 0.17,1.41 ± 0.35,1.25 ± 0.24).The calculus index (CI)of the people with type A behavior was higher than those of the people with other types of behavior (P<0.05).Conclusion:The people with tyep A behawior is easier to get periodontitis than other people.
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Objective To find out the prevalence of periodontitis in a petrochemical industry community in Ningbo ; to identify the possible factors of the prevalence; to evaluate the impact of the polluted environment on the oral health of the employees;and to provide information to the enterprises in oral diseases prevention.Methods 2 108 peoples who received regular physical examination in a petrochemical industry community in Ningbo was included.To each subject,a periodontal examination according to the principles and fundamental methods which were used in the third national oral health epidemical survey was carried out,the fast blood was phlebotomized,total cholesterol(TC),triglyceride (TG),uric acid,blood glucose and other serum indexes levels were recorded.These subjects were stratified into two age groups.Data was analyzed with x2 test and multiple regression.Results In the group of 2 108 selected subjects,the periodontitis rate was 52.3 % [95 % CI:(52.3 ± 2.1) %].In the multivariable logistic regression model,the old-age groap age(OR =4.783,P =0.000),blood pressure (OR =1.526,P =0.001) and blood glucose (OR =1.560,P =0.045) were the risk factors of periodontitis,while the environmental factor(OR =0.661) was excluded.In the young and middle-age group,blood pressure (OR =2.184,P =0.000),blood glucose (OR =2.314,P =0.001),TC(OR =1.356,P =0.003),and alcohol (OR =1.382,P =0.02) were the risk factors of periodontitis.Conclusion The levels of blood glucose,TC,blood pressure and alcohol should be considered in periodontitis prevention and the sulfureted hydrogen-based environment factor had no adverse impact on periodontitis.
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Aim: To assess the oral health related quality of life(OHQoL) of a selected population of Malaysian adults andto compare the OHQoL by periodontal status. Material& Methods: This cross-sectional study comprises aconvenient sampling of fifty subjects from the PrimaryCare Unit, Faculty of Dentistry, University of Malaya.OHQoL was assessed using the Malaysian versionof Oral Health Impact Profile-14 (OHIP-14). Basicperiodontal examination (BPE) was performed on allsubjects to determine their periodontal status. Descriptivestatistics and bivariate analysis were performed. Results:Psychological discomfort, physical pain and psychologicaldisability domains were the most affected dimensions inthis population. Subjects with income levels >RM2,500had higher impacts on their OHQoL as compared to thosefrom other income levels (p0.05). Conclusion:Subjects with high income levels had high impacts ontheir OHQoL. Those with periodontitis experiencedhigher impacts on their OHQoL as compared to those whohad a healthy periodontium or gingivitis and affected awide range of domains of quality of life.
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Clinical longevity of any prosthesis is directly related in achieving proper coronal contours. This involves close attention to detail between periodontal and prosthodontic principles during the fabrication of the prosthesis. If not done properly, iatrogenic problems may occur such as "food traps" from open contacts, overhangs, or plunging cusps. This leads to plaque accumulation, inflammation, bleeding, potential bone loss (periodontitis) thus leading to severe periodontal problems. If certain principles of placement of gingival margins and interproximal embrasures are not closely adhered to, an overcontoured restoration may act as a nidus in the rapid failure of the prosthesis.
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Objective: To study the effects of hyperbaric oxyge(HBO) in the treatment of periodontitis.Methods: 60 Guinea pigs were divided into 3 groups, 20 animals each group: ①Experimental periodontitis was induced by silk suture and feeding with the food containing 100 g/L of sugar and then exposed to 0.25 MPa of HBO for 60 min once a day when periodontitis established; ② the other 20 animals were simillary treated to group ① but not exposed to HBO; ③ another 20 animals were used as controls. HBO treatment was conducted for 2 weeks. Samples of periodontal tissues were obtained 0,4,8 and 10 weeks after treatment and prepared for histopathological study and electron microscopic observation.Results: In the treated group there were fewer macrophages in gingiva and periodontal ligment, more blood vessles, less absorption of alveolar bone, more osteoblasts and more osteogenesis in the bone. There were fewer metochodria and rough endo reticulum in plasmacytes, macrophages and osteoclasts; and more in fibroblasts, endothelial cells of blood vessles and osteoblasts. Conclusion: HBO may improve blood supply, inhibit macrophage and bone absorption.