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1.
Experimental & Molecular Medicine ; : 171-179, 2009.
Artigo em Inglês | WPRIM | ID: wpr-76613

RESUMO

Resveratrol is a polyphenolic compound in red wine that has anti-oxidant and cardioprotective effects in animal models. Reactive oxygen species (ROS) and monocyte chemotactic protein-1 (MCP-1) play key roles in foam cell formation and atherosclerosis. We studied LPS-mediated foam cell formation and the effect of resveratrol. Resveratrol pretreatment strongly suppressed LPS-induced foam cell formation. To determine if resveratrol affected the expression of genes that control ROS generation in macrophages, NADPH oxidase 1 (Nox1) was measured. Resveratrol treatment of macrophages inhibited LPS-induced Nox1 expression as well as ROS generation, and also suppressed LPS-induced MCP-1 mRNA and protein expression. We investigated the upstream targets of Nox1 and MCP-1 expression and found that Akt-forkhead transcription factors of the O class (FoxO3a) is an important signaling pathway that regulates both genes. These inhibitory effects of resveratrol on Nox1 expression and MCP-1 production may target to the Akt and FoxO3a signaling pathways.


Assuntos
Humanos , Antioxidantes/farmacologia , Células Cultivadas , Quimiocina CCL2/genética , Ativação Enzimática/efeitos dos fármacos , Células Espumosas/efeitos dos fármacos , Fatores de Transcrição Forkhead/metabolismo , Lipopolissacarídeos/farmacologia , NADH NADPH Oxirredutases/genética , Proteínas Proto-Oncogênicas c-akt/metabolismo , RNA Mensageiro/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais , Estilbenos/farmacologia
2.
The Journal of the Korean Academy of Periodontology ; : 437-444, 2008.
Artigo em Coreano | WPRIM | ID: wpr-152437

RESUMO

PURPOSE: A number of techniques and materials have been used for periodontal regeneration and bone graft procedures with guided tissue regeneration(GTR) have been suggested as alternatives to osseous surgery in the management of local infra-bony defects. However, the long-term stability and treatment outcome following bone graft procedure of infra-bony defects is poorly documented. The purpose of this study was to assess radiographic change in infra-bony defects over 2 years after bone graft procedures with various graft materials. MATERIAL AND METHODS: Patients attending the department of periodontics of Kyungpook National University Hospital were studied. Patients showed clinical and radiographic evidence of infra-bony defect(s). 44 sites of 34 patients aged 31 to 69 (mean age 48.3) were treated by bone graft procedure with a bone graft material. Baseline and 2-year follow-up radiographs were collected and evaluated for this study. Radiographic assessment includes a bone fill, bone crest change, defect resolution, and % of defect resolution. Pre- and post-treatment differences between variables (maxilla and mandible, defect depth, defect angle, bone graft materials) using the paired t-test were examined. RESULT: We observed 1.15+/-1.95 mm of bone fill, 0.40+/-1.19 mm of crestal resorption, 1.55+/-1.77 mm of defect resolution, and 40+/-44% of percentage of defect resolution. Deeper initial defect depth, narrower initial defect angle showed significantly greater bone fill, defect resolution, and % of defect resolution. But no significant difference was observed in graft sites and graft materials. CONCLUSION: If good oral hygiene maintenance and periodic recall check of patients is assured, bone graft procedure using various graft materials is one of the appropriate treatment modality for regenerative therapy of infra-bony defects.


Assuntos
Idoso , Humanos , Seguimentos , Mandíbula , Higiene Bucal , Periodontia , Regeneração , Transplantes , Resultado do Tratamento
3.
The Journal of the Korean Academy of Periodontology ; : 629-638, 2008.
Artigo em Coreano | WPRIM | ID: wpr-43840

RESUMO

PURPOSE: The purposes of this study were to compare and quantify the expression of Stromelysin-1 and MT-MMP-1 in the gingival tissues of patients with type 2 diabetes mellitus(DM) and healthy adults with chronic periodontitis. MATERIALS AND METHODS: Gingival tissue samples were obtained during periodontal surgery or tooth extraction. According to the patient's systemic condition & clinical criteria of gingiva, each gingival sample was devided into three groups. Group 1 (n=8) is clinically healthy gingiva without bleeding and no evidence of bone resorption or periodontal pockets, obtained from systemically healthy 8 patients. Group 2 (n=8) is inflammed gingiva from patients with chronic periodontitis. Group 3 (n=8) is inflammed gingiva from patients with chronic periodontitis associated with type 2 DM. Tissue samples were prepared and analyzed by Western blotting. The quantification of Stromelysin-1 and MT-MMP-1 were performed using a densitometer and statistically analyzed by one-way ANOVA followed by Tukey test. RESULTS: In the analysis of expression levels, Stromelysin-1 and MT-MMP-1 expressions were similar in group 1 and 2. Stromelysin-1 and MT-MMP-1 expressions was more increased in group 3 than group 1, 2. The difference between group 3 and group 1, 2 was statistically significant. Also, in the interrelationship of Stromelysin-1 and MT-MMP-1 expressions, expressions of Stromelysin-1 and MT-MMP-1 showed increasing tendency in chronic periodontitis associated with type 2 DM and it seems that the MT-MMP-1 expressions were increasing in proportion to Stromelysin-1 expressions. CONCLUSION: It is suggested that Stromelysin-1 and MT-MMP-1 may be partly involved in the progression of periodontal inflammation associated with type 2 DM, as related to a metabolism of other factors, such as AGE, plasmin and other inflammatory mediators. Therefore, the expression levels of Stromelysin-1 and MT-MMP-1 can be inflammatory markers of periodontal inflammed tissue with type 2 DM.


Assuntos
Adulto , Humanos , Western Blotting , Reabsorção Óssea , Periodontite Crônica , Diabetes Mellitus Tipo 2 , Fibrinolisina , Gengiva , Hemorragia , Inflamação , Metaloproteinase 14 da Matriz , Membranas , Bolsa Periodontal , Extração Dentária
4.
The Journal of the Korean Academy of Periodontology ; : 743-753, 2007.
Artigo em Coreano | WPRIM | ID: wpr-24279

RESUMO

PURPOSE: The purposes of this study were to compare and quantify the expression of MMP-3, PGE2 and IL-6 in the gingival tissues of patients with type2 diabetes mellitus and healthy adults with chronic periodontitis. MATERIAL AND METHODS: Gingival tissue samples were obtained during periodontal surgery or tooth extraction. According to the patient's systemic condition & clinical criteria of gingiva, each gingival sample was devided into three groups. Group 1(n=8) is clinically healthy gingiva without bleeding and no evidence of bone resorption or periodontal pockets, obtained from systemically healthy 8 patients. Group 2(n=8) is inflamed gingiva from patients with chronic periodontitis. Group 3(n=8) is inflamed gingiva from patients with chronic periodontitis associated with type 2 DM. Tissue samples were prepared and analyzed by Westernblotting. The quantification of MMP-3, PGE2 and IL-6 were performed using a densitometer and statistically analyzed by one-way ANOVA followed by Tukey test. RESULTS: 1. The expression levels of MMP-3 were shown highest in group 3 compared to group 1 and 2, and It showed increasing tendency in group 2 and 3. 2. The expressions of PGE2 and IL-6 were shown increasing tendency in group 2 and 3, and It was highest in group 3. 3. As expressions of MMP-3 were increased, PGE2 and IL-6 expressions showed increasing tendency in group 3 than group1 and 2, although there were no proportional relationship. CONCLUSION: This study demonstrated that the expression levels of MMP-3, PGE2 and IL-6 will be inflammatory markers of periodonta linflamed tissue and DM. It can be assumed that MMP-3 affect to expressions of PGE2 and IL-6 in progression of periodontal inflammation with alveolar bone resorption to type 2 DM.


Assuntos
Adulto , Humanos , Reabsorção Óssea , Periodontite Crônica , Diabetes Mellitus , Diabetes Mellitus Tipo 2 , Dinoprostona , Gengiva , Hemorragia , Inflamação , Interleucina-6 , Bolsa Periodontal , Extração Dentária
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