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1.
Braz Dent J ; 34(5): 43-52, 2023.
Article in English | MEDLINE | ID: mdl-38133472

ABSTRACT

This study evaluated the influence of a fluoride-modified titanium surface on osseointegration in rats with induced diabetes. One hundred and eighty rats were randomly allocated into 3 groups with 60 animals each: Control group (C): Animals without diabetes; Diabetes Group (D): Animals with uncontrolled induced diabetes; Controlled Diabetes Group (CD): Animals with diabetes induced controlled by the insulin administration. Diabetes was induced by streptozotocin injection. Each animal received 2 implants in the proximal tibial metaphysis, one with the machined surface (M) and the other one with a fluoride-modified titanium surface (F), after 4 weeks of induction of diabetes. The animals were submitted to euthanasia 2, 4, and 6 weeks after the implant placement (n = 20 animals/group). The osseointegration was evaluated by the implant removal torque test and the histometric analysis of the non-decalcified histological sections: 1) Contact bone/implant (%BIC); 2) Bone tissue area between implant threads (%BBT). Implants with F surface showed a higher removal torque than implants with surface M in all groups. There was no difference in %BIC between the groups regardless of the surface used. The F surface showed a tendency to present higher %BBT values for the 3 evaluation periods in the D group. The fluoride-modified implant surface has no impact on the %BIC and %BBT. However, the fluoride-modified implant surface increases the locking of the implants with the bone. The hyperglycemia was associated with lower removal torque values despite the surfaces of the implant used.


Subject(s)
Dental Implants , Diabetes Mellitus , Rats , Animals , Osseointegration , Fluorides , Tibia , Titanium , Surface Properties , Torque
2.
Braz. dent. j ; Braz. dent. j;34(5): 43-52, Sept.-Oct. 2023. tab, graf
Article in English | LILACS-Express | LILACS, BBO - Dentistry | ID: biblio-1528014

ABSTRACT

Abstract This study evaluated the influence of a fluoride-modified titanium surface on osseointegration in rats with induced diabetes. One hundred and eighty rats were randomly allocated into 3 groups with 60 animals each: Control group (C): Animals without diabetes; Diabetes Group (D): Animals with uncontrolled induced diabetes; Controlled Diabetes Group (CD): Animals with diabetes induced controlled by the insulin administration. Diabetes was induced by streptozotocin injection. Each animal received 2 implants in the proximal tibial metaphysis, one with the machined surface (M) and the other one with a fluoride-modified titanium surface (F), after 4 weeks of induction of diabetes. The animals were submitted to euthanasia 2, 4, and 6 weeks after the implant placement (n = 20 animals/group). The osseointegration was evaluated by the implant removal torque test and the histometric analysis of the non-decalcified histological sections: 1) Contact bone/implant (%BIC); 2) Bone tissue area between implant threads (%BBT). Implants with F surface showed a higher removal torque than implants with surface M in all groups. There was no difference in %BIC between the groups regardless of the surface used. The F surface showed a tendency to present higher %BBT values for the 3 evaluation periods in the D group. The fluoride-modified implant surface has no impact on the %BIC and %BBT. However, the fluoride-modified implant surface increases the locking of the implants with the bone. The hyperglycemia was associated with lower removal torque values despite the surfaces of the implant used.


Resumo Este estudo avaliou a influência de uma superfície de titânio modificada com flúor na osseointegração em ratos com diabetes induzida. Cento e oitenta ratos foram distribuídos aleatoriamente em 3 grupos com 60 animais cada: Grupo controle (C): Animais sem diabetes; Grupo Diabetes (D): Animais com diabetes induzida descompensada; Grupo Diabetes Controlado (CD): Animais com diabetes induzido controlado pela administração de insulina. O diabetes foi induzido por injeção de estreptozotocina. Cada animal recebeu 2 implantes na metáfise proximal da tíbia, um com superfície usinada (M) e outro com superfície de titânio modificado com flúor (F), após 4 semanas de indução do diabetes. Os animais foram submetidos à eutanásia 2, 4 e 6 semanas após a colocação do implante (n = 20 animais/grupo). A osseointegração foi avaliada pelo teste de torque de remoção do implante e pela análise histométrica dos cortes histológicos não descalcificados: 1) Contato osso-implante (%BIC); 2) Área de tecido ósseo entre as roscas do implante (%BBT). Os implantes com superfície F apresentaram maior torque de remoção do que os implantes com superfície M em todos os grupos. Não houve diferença no %BIC entre os grupos independente da superfície utilizada. A superfície F mostrou tendência a apresentar maiores valores de %BBT para os 3 períodos de avaliação no grupo D. As superfícies de implantes modificadas com flúor não influenciaram nos dados de %BIC e %BBT. Entretanto, essas superfícies aumentaram o travamento dos implantes no tecido ósseo. A hiperglicemia foi associada a menores torques de remoção dos implantes independentemente do tipo de superfície de implante utilizada.

3.
Braz Oral Res ; 34: e012, 2020.
Article in English | MEDLINE | ID: mdl-32049112

ABSTRACT

Lipoproteins are important bacterial immunostimulating molecules capable of inducing receptor activator of nuclear factor-κB (RANKL) and osteoclast formation in vitro and in vivo . Although these molecules are present in periodontopathogenic bacteria, their role in periodontitis is not known. In this study, we used Pam2CSK4 (PAM2), a synthetic molecule that mimics bacterial lipoprotein, to investigate the effects of lipoproteins on periodontitis in mice. C57BL/6 male mice were randomly divided into three experimental groups: 1) Negative control group: animals received vehicle injection; 2) Positive control group: animals received injection of Escherichia coli lipopolysaccharide (LPS); 3) PAM2 group: animals received PAM2 injection. All the injections were performed bilaterally every other day into the palatal mucosa between first and second molars. After twenty-four days, the animals were euthanized to assess alveolar bone volume (micro-CT), cellular and extracellular composition in the gingiva (stereometric analysis), and osteoclast numbers (TRAP staining). Treatment with either PAM2 or LPS induced gingival inflammation, as demonstrated by increased infiltration of inflammatory cells and enhanced angiogenesis, associated with a smaller number of fibroblasts and decreased extracellular matrix. Importantly, treatment not only with LPS but also with PAM2 resulted in a larger number of TRAP+ multinucleated osteoclasts and significant loss of alveolar bone. Collectively, our data demonstrate that PAM2 can induce gingival inflammation and bone loss in mice, broadening the avenues of investigation into the role of lipoproteins in the pathogenesis of periodontal disease.


Subject(s)
Lipopeptides/pharmacology , Periodontitis/etiology , Periodontitis/pathology , Toll-Like Receptor 2/antagonists & inhibitors , Alveolar Bone Loss/etiology , Alveolar Bone Loss/pathology , Alveolar Process/drug effects , Alveolar Process/pathology , Animals , Disease Models, Animal , Gingiva/drug effects , Gingiva/pathology , Gingivitis/etiology , Gingivitis/pathology , Male , Mice, Inbred C57BL , Osteoclasts/drug effects , Osteoclasts/physiology , Periodontitis/microbiology , Random Allocation , Tartrate-Resistant Acid Phosphatase , Time Factors , X-Ray Microtomography
4.
Braz. oral res. (Online) ; 34: e012, 2020. graf
Article in English | LILACS | ID: biblio-1089395

ABSTRACT

Abstract Lipoproteins are important bacterial immunostimulating molecules capable of inducing receptor activator of nuclear factor-κB (RANKL) and osteoclast formation in vitro and in vivo . Although these molecules are present in periodontopathogenic bacteria, their role in periodontitis is not known. In this study, we used Pam2CSK4 (PAM2), a synthetic molecule that mimics bacterial lipoprotein, to investigate the effects of lipoproteins on periodontitis in mice. C57BL/6 male mice were randomly divided into three experimental groups: 1) Negative control group: animals received vehicle injection; 2) Positive control group: animals received injection of Escherichia coli lipopolysaccharide (LPS); 3) PAM2 group: animals received PAM2 injection. All the injections were performed bilaterally every other day into the palatal mucosa between first and second molars. After twenty-four days, the animals were euthanized to assess alveolar bone volume (micro-CT), cellular and extracellular composition in the gingiva (stereometric analysis), and osteoclast numbers (TRAP staining). Treatment with either PAM2 or LPS induced gingival inflammation, as demonstrated by increased infiltration of inflammatory cells and enhanced angiogenesis, associated with a smaller number of fibroblasts and decreased extracellular matrix. Importantly, treatment not only with LPS but also with PAM2 resulted in a larger number of TRAP+ multinucleated osteoclasts and significant loss of alveolar bone. Collectively, our data demonstrate that PAM2 can induce gingival inflammation and bone loss in mice, broadening the avenues of investigation into the role of lipoproteins in the pathogenesis of periodontal disease.


Subject(s)
Animals , Male , Periodontitis/etiology , Periodontitis/pathology , Toll-Like Receptor 2/antagonists & inhibitors , Lipopeptides/pharmacology , Osteoclasts/drug effects , Osteoclasts/physiology , Periodontitis/microbiology , Time Factors , Random Allocation , Alveolar Bone Loss/etiology , Alveolar Bone Loss/pathology , Disease Models, Animal , X-Ray Microtomography , Alveolar Process/drug effects , Alveolar Process/pathology , Tartrate-Resistant Acid Phosphatase , Gingiva/drug effects , Gingiva/pathology , Gingivitis/etiology , Gingivitis/pathology , Mice, Inbred C57BL
5.
ROBRAC ; 28(84): 23-25, jan./mar. 2019. Ilus
Article in Portuguese | LILACS | ID: biblio-1049216

ABSTRACT

Objetivo: apresentar um caso clínico de instalação de implante imediato em região de bifurcação após exodontia de molar com uma técnica de osteotomia alternativa com o preparo do sitio implantar previamente à remoção das raízes. Materiais e métodos: em dezembro de 2017, JNPS, 39 anos de idade, sexo masculino, compareceu à Faculdade de Odontologia com queixa do dente 46 fraturado sem sintomatologia dolorosa. Nos exames clínicos e radiográficos o dente 46 apresentava tratamento endodôntico, sem remanescente coronário e amplo septo inter-radicular que favorecia a instalação de implante imediato. A cirurgia ocorreu em fevereiro de 2018 com o preparo do leito do implante na região do centro do dente previamente à exodontia. Em seguida foi realizada a extração das raízes de forma minimamente traumática, visando preservar a estrutura circundante. Foi utilizado um implante Cone Morse 3,75x9mm (Titamax CM Cortical ­ Neodent, Curitiba, Brasil). O torque final de inserção foi de 20 N/cm e foi instalado o cicatrizador para procedimento cirúrgico de 1 estágio. Após 4 meses foi instalado o pilar protético (Pilar CM ­ Neodent, Curitiba, Brasil) com altura de 2,5 mm e nas sessões seguintes foram realizados os procedimentos para confecção de coroa metalocerâmica. Resultados: no acompanhamento de 12 meses após instalação do implante, verificou-se aspectos clínicos e radiográficos de normalidade, além de satisfação do paciente com o tratamento. Conclusão: a técnica utilizada facilita o preparo do leito receptor e a instalação de implante em condições de estabilidade favorável, podendo ser empregada em situações clínicas semelhantes.


Objective: to present a case report of immediate implant surgery in the region of an extensively damaged molar using an alternative osteotomy technique with bone drilling prior to root extraction. Materials and methods: in December 2017 JNPS, 39-years-old male patient, attended to the Faculty of Dentistry, complaining about a fractured tooth without pain symptoms. At clinical and radiographic exams, tooth #46 was endodontically treated without coronal structure and wide inter-radicular septum, favoring the insertion of an immediate implant. Implant surgery was performed in February 2018 by drilling the implant bone site in the central region of the tooth prior to extraction. Then, the roots were extracted using minimally traumatic procedures, aiming to preserve the surrounding bone structure. A 3.75x9 mm morse taper implant (Titamax CM Cortical, Neodent, Curitiba, Brazil) was inserted. The final insertion torque was 20 N/cm was obtained and a healing cap was installed for a onestage surgical procedure. After 4 months, a 2.5mm height prosthetic abutment (Pilar CM - Neodent, Curitiba, Brazil) was installed and in the following appointments the procedures for fabrication of a metalceramic crown were performed. Results: in the 12-month follow-up, clinical and radiographic aspects of normality were observed, and patient reported satisfaction with the treatment. Conclusion: the technique used in this clinical case facilitated the bone preparation for implant insertion, preserving bone structure for a favorable implant stability, and may be recommended for similar clinical situations.

6.
J Appl Oral Sci ; 25(6): 689-699, 2017.
Article in English | MEDLINE | ID: mdl-29211291

ABSTRACT

MATERIAL AND METHODS: Periodontal regeneration is still a challenge in terms of predictability and magnitude of effect. In this study we assess the biological effects of combining chemical root conditioning and biological mediators on three relevant cell types for periodontal regeneration. Bovine dentin slices were conditioned with 25% citric acid followed by topical application of basic fibroblast growth factor (bFGF, 10 and 50 ng). We used ELISA to assess the dynamics of bFGF release from the dentin surface and RT-qPCR to study the expression of Runx2, Col1a1, Bglap and fibronectin by periodontal ligament (PDL) fibroblasts, cementoblasts and bone marrow stromal cells (BMSC) grown onto these dentin slices. We also assessed the effects of topical application of bFGF on cell proliferation by quantification of genomic DNA. RESULTS: Acid conditioning significantly increased the release of bFGF from dentin slices. Overall, bFGF application significantly (p<0.05) increased cell proliferation, except for BMSC grown on non-conditioned dentin slices. Dentin substrate discretely increased expression of Col1a1 in all cell types. Expression of Runx2, Col1a1 and Fn was either unaffected or inhibited by bFGF application in all cell types. We could not detect expression of the target genes on BMSC grown onto conditioned dentin. CONCLUSION: Acid conditioning of dentin improves the release of topically-applied bFGF. Topical application of bFGF had a stimulatory effect on proliferation of PDL fibroblasts, cementoblasts and BMSC, but did not affect expression of Runx2, Col1a1, Bglap and fibronectin by these cells.


Subject(s)
Cell Proliferation/drug effects , Dentin/drug effects , Fibroblast Growth Factor 2/pharmacology , Periodontal Ligament/drug effects , Regeneration/drug effects , Animals , Cattle , Fibroblast Growth Factor 2/administration & dosage , Gene Expression , Periodontal Ligament/metabolism
7.
J. appl. oral sci ; J. appl. oral sci;25(6): 689-699, Nov.-Dec. 2017. graf
Article in English | LILACS, BBO - Dentistry | ID: biblio-893665

ABSTRACT

Abstract Periodontal regeneration is still a challenge in terms of predictability and magnitude of effect. In this study we assess the biological effects of combining chemical root conditioning and biological mediators on three relevant cell types for periodontal regeneration. Material and Methods: Bovine dentin slices were conditioned with 25% citric acid followed by topical application of basic fibroblast growth factor (bFGF, 10 and 50 ng). We used ELISA to assess the dynamics of bFGF release from the dentin surface and RT-qPCR to study the expression of Runx2, Col1a1, Bglap and fibronectin by periodontal ligament (PDL) fibroblasts, cementoblasts and bone marrow stromal cells (BMSC) grown onto these dentin slices. We also assessed the effects of topical application of bFGF on cell proliferation by quantification of genomic DNA. Results: Acid conditioning significantly increased the release of bFGF from dentin slices. Overall, bFGF application significantly (p<0.05) increased cell proliferation, except for BMSC grown on non-conditioned dentin slices. Dentin substrate discretely increased expression of Col1a1 in all cell types. Expression of Runx2, Col1a1 and Fn was either unaffected or inhibited by bFGF application in all cell types. We could not detect expression of the target genes on BMSC grown onto conditioned dentin. Conclusion: Acid conditioning of dentin improves the release of topically-applied bFGF. Topical application of bFGF had a stimulatory effect on proliferation of PDL fibroblasts, cementoblasts and BMSC, but did not affect expression of Runx2, Col1a1, Bglap and fibronectin by these cells.


Subject(s)
Animals , Cattle , Periodontal Ligament/drug effects , Regeneration/drug effects , Fibroblast Growth Factor 2/pharmacology , Dentin/drug effects , Cell Proliferation/drug effects , Periodontal Ligament/metabolism , Gene Expression , Fibroblast Growth Factor 2/administration & dosage
8.
Braz Oral Res ; 31: e75, 2017 Sep 28.
Article in English | MEDLINE | ID: mdl-29019549

ABSTRACT

This study aimed to characterize the dynamics of suppressor of cytokine signaling (SOCS1) expression in a rat model of lipopolysaccharide-induced periodontitis. Wistar rats in the experimental groups were injected three times/week with LPS from Escherichia coli on the palatal aspect of the first molars, and control animals were injected with vehicle (phosphate-buffered saline). Animals were sacrificed 7, 15, and 30 days after the first injection to analyze inflammation (stereometric analysis), bone loss (macroscopic analysis), gene expression (qRT-PCR), and protein expression/activation (Western blotting). The severity of inflammation and bone loss associated with LPS-induced periodontitis increased from day 7 to day 15, and it was sustained through day 30. Significant (p < 0.05) increases in SOCS1, RANKL, OPG, and IFN-γ gene expression were observed in the experimental group versus the control group at day 15. SOCS1 protein expression and STAT1 and NF-κB activation were increased throughout the 30-day experimental period. Gingival tissues affected by experimental periodontitis express SOCS1, indicating that this protein may potentially downregulate signaling events involved in inflammatory reactions and bone loss and thus may play a relevant role in the development and progression of periodontal disease.


Subject(s)
Alveolar Bone Loss/pathology , Periodontitis/pathology , Suppressor of Cytokine Signaling 1 Protein/analysis , Alveolar Bone Loss/etiology , Alveolar Bone Loss/metabolism , Animals , Blotting, Western , Immunohistochemistry , Interferon-gamma/analysis , Lipopolysaccharides , Male , NF-kappa B/analysis , Periodontitis/etiology , Periodontitis/metabolism , RANK Ligand/analysis , Random Allocation , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , STAT1 Transcription Factor/analysis , Time Factors
10.
Braz Oral Res ; 31: e28, 2017 04 10.
Article in English | MEDLINE | ID: mdl-28403331

ABSTRACT

The purpose of this study is to evaluate the effect of the avocado/soybean unsaponifiables (ASU) on the treatment of induced periodontitis in rats. Periodontitis was induced in 84 rats via ligature placement around the second upper molar, which was removed after 7 days, and scaling and root planning (SRP) was performed at this time. Subsequently, the rats were randomly allocated to four groups with 21 animals each: One SRP group in which saline solution was administered (SS), and three groups in which ASU was administered (0.6 g/kg/day), beginning either 7 days before the induction of periodontitis (SRP/ASU-7), on the day of periodontitis induction (SRP/ASU0), or on the day of treatment (SRP/ASU+7). ASU and SS were administered daily by gavage until the sacrifice of the animals (7, 15, and 30 days after SRP). The % bone in the furcation area was evaluated by histomorphometry and micro-CT. The expression of proteins (TRAP, RANKL, and alkaline phosphatase) and mRNA (IL-1ß, TNF-α, IL-6, RANKL, and alkaline phosphatase) were evaluated by immunohistochemistry and qPCR. The SRP/ASU+7 group presented a higher percentage of bone fill in the furcation area and higher expression of alkaline phosphatase than in the SRP group (at 7 and 30 days, respectively). The SRP/ASU0 and SRP/ASU+7 groups presented lower expression levels of RANKL mRNA than the SRP and SRP/ASU-7 groups at 15 days. ASU administration on the day of the SRP treatment of the ligature-induced periodontitis promoted subtle beneficial effects on periodontal repair following the treatment of induced periodontitis within the experimental period of 7 days.


Subject(s)
Glycine max/chemistry , Periodontitis/drug therapy , Persea/chemistry , Plant Extracts/therapeutic use , Animals , Gene Expression , Immunohistochemistry , Interleukin-1beta/analysis , Interleukin-6/analysis , Male , Periodontitis/etiology , Periodontitis/pathology , RANK Ligand/analysis , Random Allocation , Rats, Sprague-Dawley , Real-Time Polymerase Chain Reaction , Reference Values , Reproducibility of Results , Root Planing/methods , Tartrate-Resistant Acid Phosphatase/analysis , Time Factors , Treatment Outcome , Tumor Necrosis Factor-alpha/analysis
11.
Braz. oral res. (Online) ; 31: e75, 2017. tab, graf
Article in English | LILACS | ID: biblio-952120

ABSTRACT

Abstract This study aimed to characterize the dynamics of suppressor of cytokine signaling (SOCS1) expression in a rat model of lipopolysaccharide-induced periodontitis. Wistar rats in the experimental groups were injected three times/week with LPS from Escherichia coli on the palatal aspect of the first molars, and control animals were injected with vehicle (phosphate-buffered saline). Animals were sacrificed 7, 15, and 30 days after the first injection to analyze inflammation (stereometric analysis), bone loss (macroscopic analysis), gene expression (qRT-PCR), and protein expression/activation (Western blotting). The severity of inflammation and bone loss associated with LPS-induced periodontitis increased from day 7 to day 15, and it was sustained through day 30. Significant (p < 0.05) increases in SOCS1, RANKL, OPG, and IFN-γ gene expression were observed in the experimental group versus the control group at day 15. SOCS1 protein expression and STAT1 and NF-κB activation were increased throughout the 30-day experimental period. Gingival tissues affected by experimental periodontitis express SOCS1, indicating that this protein may potentially downregulate signaling events involved in inflammatory reactions and bone loss and thus may play a relevant role in the development and progression of periodontal disease.


Subject(s)
Animals , Male , Periodontitis/pathology , Alveolar Bone Loss/pathology , Suppressor of Cytokine Signaling 1 Protein/analysis , Periodontitis/etiology , Periodontitis/metabolism , Time Factors , Immunohistochemistry , Random Allocation , Lipopolysaccharides , Blotting, Western , Alveolar Bone Loss/etiology , Alveolar Bone Loss/metabolism , NF-kappa B/analysis , Interferon-gamma/analysis , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , STAT1 Transcription Factor/analysis , RANK Ligand/analysis
12.
Braz. oral res. (Online) ; 31: e28, 2017. tab, graf
Article in English | LILACS | ID: biblio-839509

ABSTRACT

Abstract The purpose of this study is to evaluate the effect of the avocado/soybean unsaponifiables (ASU) on the treatment of induced periodontitis in rats. Periodontitis was induced in 84 rats via ligature placement around the second upper molar, which was removed after 7 days, and scaling and root planning (SRP) was performed at this time. Subsequently, the rats were randomly allocated to four groups with 21 animals each: One SRP group in which saline solution was administered (SS), and three groups in which ASU was administered (0.6 g/kg/day), beginning either 7 days before the induction of periodontitis (SRP/ASU-7), on the day of periodontitis induction (SRP/ASU0), or on the day of treatment (SRP/ASU+7). ASU and SS were administered daily by gavage until the sacrifice of the animals (7, 15, and 30 days after SRP). The % bone in the furcation area was evaluated by histomorphometry and micro-CT. The expression of proteins (TRAP, RANKL, and alkaline phosphatase) and mRNA (IL-1β, TNF-α, IL-6, RANKL, and alkaline phosphatase) were evaluated by immunohistochemistry and qPCR. The SRP/ASU+7 group presented a higher percentage of bone fill in the furcation area and higher expression of alkaline phosphatase than in the SRP group (at 7 and 30 days, respectively). The SRP/ASU0 and SRP/ASU+7 groups presented lower expression levels of RANKL mRNA than the SRP and SRP/ASU-7 groups at 15 days. ASU administration on the day of the SRP treatment of the ligature-induced periodontitis promoted subtle beneficial effects on periodontal repair following the treatment of induced periodontitis within the experimental period of 7 days.


Subject(s)
Animals , Male , Periodontitis/drug therapy , Glycine max/chemistry , Plant Extracts/therapeutic use , Persea/chemistry , Periodontitis/etiology , Periodontitis/pathology , Reference Values , Time Factors , Immunohistochemistry , Random Allocation , Gene Expression , Reproducibility of Results , Interleukin-6/analysis , Tumor Necrosis Factor-alpha/analysis , Treatment Outcome , Root Planing/methods , Rats, Sprague-Dawley , Interleukin-1beta/analysis , RANK Ligand/analysis , Real-Time Polymerase Chain Reaction , Tartrate-Resistant Acid Phosphatase/analysis
13.
Perionews ; 7(2): 162-168, 2013. ilus
Article in Portuguese | LILACS, BBO - Dentistry | ID: lil-689061

ABSTRACT

Algumas regiões da cavidade oral apresentam condições anatômicas que parecem interferir negativamente no resultado do recobrimento de recessões gengivais. Dessa forma, o objetivo desse relato de caso foi apresentar duas cirurgias de recobrimento de recessões gengivais em dentes mandibulares executadas no mesmo paciente com o acompanhamento de 24 meses. Paciente RP, 35 anos, gênero masculino, leucoderma, não fumante, sistematicamente saudável, procurou atendimento na clínica do curso de especialização em Periodontia da Faculdade de Odontologia de Araraquara – Foar-Unesp. Sua queixa principal eram recessões inferiores nos dentes 33, 34, 35 e 43, 44 e 45. Além do incômodo estético, o paciente relatava sensibilidade dentinária ocasional. Para resolução do caso foi indicada a técnica de enxerto conjuntivo subepitelial associada ao retalho pediculado reposicionado coronalmente. Após dois anos do procedimento cirúrgico, percebeu-se excelente recobrimento radicular com significante melhora estética do caso. Pôde-se concluir que a técnica de enxerto conjuntivo subepitelial foi eficaz no recobrimento de recessões gengivais do tipo Classe I de Miller, mesmo em uma região de difícil execução da técnica.


Subject(s)
Humans , Male , Adult , Connective Tissue , Esthetics, Dental , Free Tissue Flaps , Gingival Recession
14.
Araraquara; s.n; 2013. 99 p. ilus, tab.
Thesis in Portuguese | LILACS, BBO - Dentistry | ID: biblio-867814

ABSTRACT

As interações microrganismo-hospedeiro se iniciam pela detecção de padrões moleculares associados a microrganismos (MAMPs) por receptores semelhantes à Toll (TLR) e por proteínas com domínio de ligação à nucleotídeos e oligomerização (Nod) na resposta imune inata. No entanto, como a cavidade bucal saudável é continuamente colonizada por microrganismos não patogênicos que também apresentam MAMPs, deve haver um mecanismo endógeno de regulação negativa da resposta do hospedeiro para evitar uma resposta exagerada e desnecessária com consequências negativas ao hospedeiro. Os mecanismos associados à distinção de microrganismos comensais e patogênicos na mucosa bucal são ainda pouco compreendidos. As proteínas Nod foram inicialmente descritas como 'TLRs intracelulares' capazes de reconhecer MAMPs no citosol; no entanto, estudos in vitro indicam que Nod têm papel relevante na regulação da expressão de RANKL e OPG induzidas por antígenos microbianos, bem como na modulação da atividade de vias de sinalização intracelular associadas à expressão de citocinas diretamente relacionadas à regulação do turnover do tecido ósseo. Devido à escassez de informações sobre o papel das proteínas Nod na modulação das interações microrganismo-hospedeiro na mucosa oral e com base nestas informações, nossa hipótese é que as proteínas Nod tem um papel relevante na modulação da reação inflamatória e suas consequências, incluindo a reabsorção do osso alveolar. Para testar esta hipótese, os objetivos específicos propostos foram: avaliar em camundongos knockout para Nod1, Nod2 ou Rip2, através de microtomografia computadorizada e avaliações histológicas descritivas, estereométricas e imunohistoquímicas (TRAP), o papel das proteínas Nod na inflamação e reabsorção óssea associadas à doença periodontal experimental induzida por bactérias inativadas por calor. A influência das proteínas Nod nas redes de citocinas e na sinalização intracelular associadas com a doença periodontal foi determinada in vitro em culturas primárias de macrófagos através de ensaios baseados nas plataformas ELISA e PCR em tempo real. Nossos resultados mostraram que, enquanto que nos camundongos Nod1 KO a reabsorção óssea alveolar e o número de osteoclastos aumentou significantemente, a deleção de Nod2 causou efeito contrário, diminuindo a reabsorção óssea. Os resultados in vitro foram correspondentes com os dados in vivo no caso de Nod2 (qPCR array, ELISA citocinas e vias de sinalização) e distintos no caso Nod1 (ELISA citocinas e vias de sinalização). Estes resultados demonstram que as proteínas Nod tem papel relevante na modulação das interações bactéria-hospedeiro associadas à doença periodontal induzida por bactérias inativadas por calor. Enquanto Nod1 parece exercer papel protetor na inflamação e reabsorção óssea, Nod2 atua como amplificador da resposta do hospedeiro


Recognition of pathogenic bacteria by the host is initially mediated by the innate immune response through detection of microbe-associated molecular pattern (MAMPs) by Toll-like receptors (TLR) and Nucleotide-oligomerization domain (Nod) proteins. Since the oral cavity, as well as other mucosal surfaces, is continuously colonized with non-pathogenic bacteria that also present MAMPs, there has to be an endogenous negative regulatory mechanism in place to prevent an overt host response with deleterious consequences. Specifically in the oral mucosa, it is not clear how the immune system is able to quickly distinguish between commensal and pathogenic bacteria and tailor the host response. Nod proteins were initially described as 'intracellular TLRs' that recognize MAMPs associated with bacteria invading the cytosol; however these proteins have been shown to modulate the activation of various signaling pathways involved in the expression of inflammatory genes, including MAPK and NF-κB in concert with TLR stimulation. There is paucity of information on the in vivo role of Nod proteins in the modulation of host-microbe interactions in the oral mucosa. Based on this information, our hypothesis is that Nod proteins play an important role in the modulation of the inflammatory reaction associated with periodontal diseases and its consequences, including alveolar bone resorption. To test this hypothesis, we propose the following specific aims: Assess the role of Nod proteins in the inflammation and bone resorption in experimentally-induced periodontal disease. Describe the influence of Nod proteins on the cytokine and signaling networks associated with periodontal disease


Subject(s)
In Vitro Techniques , Nod Signaling Adaptor Proteins , Periodontal Diseases , Bone Resorption
15.
J Appl Oral Sci ; 20(2): 128-38, 2012.
Article in English | MEDLINE | ID: mdl-22666826

ABSTRACT

Recently, new treatment approaches have been developed to target the host component of periodontal disease. This review aims at providing updated information on host-modulating therapies, focusing on treatment strategies for inhibiting signal transduction pathways involved in inflammation. Pharmacological inhibitors of MAPK, NFκB and JAK/STAT pathways are being developed to manage rheumatoid arthritis, periodontal disease and other inflammatory diseases. Through these agents, inflammatory mediators can be inhibited at cell signaling level, interfering on transcription factors activation and inflammatory gene expression. Although these drugs offer great potential to modulate host response, their main limitations are lack of specificity and developments of side effects. After overcoming these limitations, adjunctive host modulating drugs will provide new therapeutic strategies for periodontal treatment.


Subject(s)
Inflammation Mediators/antagonists & inhibitors , Intracellular Signaling Peptides and Proteins/therapeutic use , Molecular Targeted Therapy/methods , Periodontal Diseases/therapy , Signal Transduction/drug effects , Biofilms , Humans , Inflammation Mediators/immunology , Inflammation Mediators/metabolism , Intracellular Signaling Peptides and Proteins/immunology , Janus Kinases/immunology , Janus Kinases/metabolism , Mitogen-Activated Protein Kinases/immunology , Mitogen-Activated Protein Kinases/metabolism , NF-kappa B/immunology , NF-kappa B/metabolism , Periodontal Diseases/etiology , Periodontal Diseases/immunology , STAT Transcription Factors/immunology , STAT Transcription Factors/metabolism
16.
J. appl. oral sci ; J. appl. oral sci;20(2): 128-138, Mar.-Apr. 2012. ilus, tab
Article in English | LILACS | ID: lil-626410

ABSTRACT

Recently, new treatment approaches have been developed to target the host component of periodontal disease. This review aims at providing updated information on host-modulating therapies, focusing on treatment strategies for inhibiting signal transduction pathways involved in inflammation. Pharmacological inhibitors of MAPK, NFκB and JAK/STAT pathways are being developed to manage rheumatoid arthritis, periodontal disease and other inflammatory diseases. Through these agents, inflammatory mediators can be inhibited at cell signaling level, interfering on transcription factors activation and inflammatory gene expression. Although these drugs offer great potential to modulate host response, their main limitations are lack of specificity and developments of side effects. After overcoming these limitations, adjunctive host modulating drugs will provide new therapeutic strategies for periodontal treatment.


Subject(s)
Humans , Inflammation Mediators/antagonists & inhibitors , Intracellular Signaling Peptides and Proteins/therapeutic use , Molecular Targeted Therapy/methods , Periodontal Diseases/therapy , Signal Transduction/drug effects , Biofilms , Inflammation Mediators/immunology , Inflammation Mediators/metabolism , Intracellular Signaling Peptides and Proteins/immunology , Janus Kinases/immunology , Janus Kinases/metabolism , Mitogen-Activated Protein Kinases/immunology , Mitogen-Activated Protein Kinases/metabolism , NF-kappa B/immunology , NF-kappa B/metabolism , Periodontal Diseases/etiology , Periodontal Diseases/immunology , STAT Transcription Factors/immunology , STAT Transcription Factors/metabolism
17.
J Appl Oral Sci ; 20(1): 76-81, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22437682

ABSTRACT

UNLABELLED: Furcation involvement in periodontal disease has been a challenge for the dentist. OBJECTIVE: The aim of this study was to investigate root dimensions in the furcation area of 233 mandibular first molars. MATERIAL AND METHODS: Digital photomicrographs were used to obtain the following measurements on the buccal and lingual surfaces of each tooth: root trunk height (RT), horizontal interadicular distance obtained 1 mm (D1) and 2 mm (D2) below the fornix and interadicular angle (IA). RESULTS: Mean ± standard deviation of buccal and lingual furcation measurements were, respectively, 1.37 ± 0.78 mm and 2.04 ± 0.89 mm for RT; 0.86 ± 0.39 mm and 0.71 ± 0.42 mm for D1; 1.50 ± 0.48 mm and 1.38 ± 0.48 mm for D2; 41.68 ± 13.20° and 37.78 ± 13.18° for IA. Statistically significant differences were found between all measured parameters for buccal and lingual sides (p<0.05, paired t test). CONCLUSIONS: In conclusion, the lingual furcation of mandibular first molars presented narrower entrance and longer root trunk than the buccal furcation, suggesting more limitation for instrumentation and worse prognosis to lingual furcation involvements in comparison to buccal lesions.


Subject(s)
Furcation Defects/pathology , Molar/anatomy & histology , Tooth Root/anatomy & histology , Humans , Mandible , Odontometry , Organ Size , Reference Values
18.
J. appl. oral sci ; J. appl. oral sci;20(1): 76-81, Jan.-Feb. 2012. ilus, graf
Article in English | LILACS | ID: lil-618157

ABSTRACT

Furcation involvement in periodontal disease has been a challenge for the dentist. OBJECTIVE: The aim of this study was to investigate root dimensions in the furcation area of 233 mandibular first molars. MATERIAL AND METHODS: Digital photomicrographs were used to obtain the following measurements on the buccal and lingual surfaces of each tooth: root trunk height (RT), horizontal interadicular distance obtained 1 mm (D1) and 2 mm (D2) below the fornix and interadicular angle (IA). RESULTS: Mean± standard deviation of buccal and lingual furcation measurements were, respectively, 1.37±0.78 mm and 2.04±0.89 mm for RT; 0.86±0.39 mm and 0.71±0.42 mm for D1; 1.50±0.48 mm and 1.38±0.48 mm for D2; 41.68±13.20° and 37.78±13.18° for IA. Statistically significant differences were found between all measured parameters for buccal and lingual sides (p<0.05, paired t test). CONCLUSIONS: In conclusion, the lingual furcation of mandibular first molars presented narrower entrance and longer root trunk than the buccal furcation, suggesting more limitation for instrumentation and worse prognosis to lingual furcation involvements in comparison to buccal lesions.


Subject(s)
Humans , Furcation Defects/pathology , Molar/anatomy & histology , Tooth Root/anatomy & histology , Mandible , Odontometry , Organ Size , Reference Values
19.
Braz. dent. j ; Braz. dent. j;23(6): 758-763, 2012. ilus
Article in English | LILACS | ID: lil-662439

ABSTRACT

One of the main purposes of mucogingival therapy is to obtain full root coverage. Several treatment modalities have been developed, but few techniques can provide complete root coverage in a class III Miller recession. Thus, the aim of this case report is to present a successful clinical case of a Miller class III gingival recession in which complete root coverage was obtained by means of a multidisciplinary approach. A 17-year-old Caucasian female was referred for treatment of a gingival recession on the mandibular left central incisor. The following procedures were planned for root coverage in this case: free gingival graft, orthodontic movement by means of alignment and leveling and coronally advanced flap (CAF). The case has been followed up for 12 years and the patient presents no recession, no abnormal probing depth and no bleeding on probing, with a wide attached gingiva band. A compromised tooth with poor prognosis, which would be indicated for extraction, can be treated by orthodontic movement and periodontal therapy, with possibility of 100% root coverage in some class III recessions.


Um dos principais objetivos da terapia mucogengival é atingir a cobertura completa da raiz. Diversas modalidades de tratamento têm sido desenvolvidas, mas poucas técnicas podem obter a cobertura total da raiz em uma recessão gengival classe III de Miller. Assim, o objetivo deste relato é apresentar um caso de sucesso clínico de uma recessão gengival classe III de Miller na qual foi obtida a cobertura completa da raiz por meio de uma abordagem multidisciplinar. Uma jovem de 17 anos sexo feminino, leucoderma, foi encaminhada para tratamento de uma recessão gengival no incisivo central inferior esquerdo. Para a cobertura radicular foi planejado: enxerto gengival livre, movimento ortodôntico por meio de alinhamento e nivelamento e retalho reposicionado coronariamente (CAF). Este caso tem sido acompanhado por 12 anos e o paciente apresenta ausência de recessão, sem profundidade de sondagem anormal e sem sangramento à sondagem com ampla faixa de gengiva inserida. Dentes comprometidos e com mau prognóstico, que seriam extraídos em muitos casos, podem ser tratados por meio de movimento ortodôntico e terapia periodontal. 100% de cobertura da raiz é possível e pode ser conseguida em alguns casos de recessão gengival classe III.


Subject(s)
Adolescent , Female , Humans , Free Tissue Flaps/transplantation , Gingiva/transplantation , Gingival Recession/surgery , Tooth Movement Techniques/methods , Autografts , Alveolar Bone Loss/surgery , Combined Modality Therapy , Esthetics, Dental , Follow-Up Studies , Gingiva/pathology , Gingival Recession/classification , Gingivitis/surgery , Incisor/surgery , Malocclusion/therapy , Surgical Flaps/transplantation , Treatment Outcome , Tooth Root/surgery
20.
Perionews ; 5(2): 146-150, mar.-abr. 2011. ilus
Article in Portuguese | LILACS | ID: lil-688136

ABSTRACT

As recessões gengivais são lesões caracterizadas por uma migração apical da margem gengival com consequente exposição da superfície radicular, que constitui um problema estético para o paciente. Várias técnicas cirúrgicas têrr sido indicadas para o recobrimento das recessões gengivais, sendo a técnica de enxerto de tecido conjuntivo a de maior previsibilidade de recobrimentc e de melhores resultados estéticos e menores efeitos colaterais pós-operatórios em relação ao enxerto gengival livre epitelizado. 0 objetivo da descriçãc desse caso clínico foi de descrever a técnica de enxerto gengival livre sube-pitelizado demonstrando seu resultado no recobrimento de uma recessãc Classe l de Miller. Após dois anos percebe-se excelente recobrimento radicular com significante melhora estética do caso. A técnica de enxerto gengival livre subepitelial foi eficaz no recobrimento de recessão Classe l de Miller apresentada nesse caso clínico.


Subject(s)
Humans , Male , Adult , Esthetics , Gingival Recession , Gingival Recession/surgery , Tissue Transplantation , Connective Tissue/transplantation
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