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1.
Int Endod J ; 52(2): 149-157, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30091243

ABSTRACT

AIM: To evaluate the mRNA expression levels of the cytokines interferon-γ, tumour necrosis factor-α, interleukin (IL)-1ß, IL-10, IL-6, VEGF, and AGT and the chemokine CCL2/MCP-1 in periapical interstitial fluid associated with root canal infections before and after the reduction of the bacterial load using a cleaning procedure. METHODOLOGY: The case group included 11 patients with chronic liver disease, and the control group included 11 healthy patients. Clinical samples were taken from teeth with pulp necrosis. After cleaning and drying the canal, three paper points were introduced into the root canal and passed through the root apex (2 mm) into the periapical tissues for 1 min. The samples were collected immediately after root canal cleaning and 7 days later to characterize those gene expression levels using real-time PCR. The data were subjected to the Shapiro-Wilk and the Wilcoxon tests. RESULTS: In the control group, significantly increased expression of the pro-inflammatory cytokines IFN-γ and TNF-α was observed in teeth with restrained bacterial loads (day 7) (P < 0.05). Similarly, increased TNF-α expression was found on day 7 in the liver group (P < 0.05). No differences were observed in the expression levels of the IL-1ß, IL-10 and, IL-6, MCP-1/CCL-2 and VEGF between the first collection (day 0) and second collection (day 7), over time in either group. CONCLUSION: Chronic liver disease patients exhibited sufficient immunologic ability showing relatively similar expression levels of cytokines, chemokines and angiogenic factors in periapical samples compared with the responses from no-chronic liver disease patients. The outcomes of this study suggest that liver impairment did not compromise the periapical immune response.


Subject(s)
Chemokines/metabolism , Cytokines/metabolism , Liver Diseases/complications , Liver Diseases/immunology , Periapical Diseases/immunology , Root Canal Therapy , Tooth/immunology , Adult , Aged , Bacterial Load , Chemokine CCL2/metabolism , Dental Pulp Cavity/microbiology , Dental Pulp Necrosis/immunology , Female , Humans , Interferon-gamma/metabolism , Interleukin-10/metabolism , Interleukin-1beta/metabolism , Interleukin-6/metabolism , Male , Middle Aged , Periapical Tissue/immunology , Periapical Tissue/microbiology , RNA, Messenger/metabolism , Tooth Apex , Tumor Necrosis Factor-alpha/metabolism , Vascular Endothelial Growth Factor A/metabolism
2.
J Endod ; 39(7): 889-92, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23791257

ABSTRACT

INTRODUCTION: Root canal treatment typically involves cleaning and shaping procedures followed by treatment with antibacterial endodontic dressing between appointments and, ultimately, 3-dimensional,hermetic filling. Chlorhexidine (CHX) is effective as an irrigation solution and is used as an endodontic dressing. The aim of this study was to examine the influence of CHX on periapical cytokine expression. METHODS: Expression levels of the cytokines interferon γ, tumor necrosis factor α, interleukin (IL)-1ß, IL-17A, IL-10, and the chemokine monocyte chemoattractant protein-1 (CCL2/MCP-1) were assayed by real-time polymerase chain reaction immediately after root canal cleaning and 15 days later. RESULTS: Messenger RNA expression of IL-1ß, interferon γ, IL-10, and CCL2/MCP-1 was increased on day 15 in teeth without endodontic dressing. No statistical change was observed in the messenger RNA expression of cytokines when comparing sampling times for teeth that received endodontic dressing. CONCLUSIONS: The results show that CHX application between appointments prevented the increase of both proinflammatory and immunoregulatory cytokines 15 days after the dental procedure.


Subject(s)
Chlorhexidine/pharmacology , Cytokines/drug effects , Periapical Tissue/drug effects , Root Canal Irrigants/pharmacology , Root Canal Preparation/methods , Tooth/drug effects , Chemokine CCL2/analysis , Cytokines/analysis , Dental Pulp Necrosis/immunology , Dental Pulp Necrosis/therapy , Follow-Up Studies , Humans , Inflammation Mediators/analysis , Interferon-gamma/drug effects , Interleukin-1/analysis , Interleukin-10/analysis , Interleukin-17/analysis , Periapical Tissue/immunology , RNA, Messenger/drug effects , Tooth/immunology
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