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1.
Braz. dent. j ; 28(6): 704-709, Nov.-Dec. 2017. tab, graf
Article in English | LILACS | ID: biblio-888699

ABSTRACT

Abstract This study determined the oxygen saturation (SaO2) in dental pulp of healthy maxillary and mandibular molars. Mean of SaO2 was evaluated in 112 maxillary and mandibular molars using pulse oximetry. Quantitative variables were described by mean and standard deviation. Variables with symmetric distribution were compared by Student t test and Mann-Whitney test. Pearson's correlation coefficient was used to correlate quantitative variables. Analysis of variance was used to assess differences in SaO2 levels between the molar groups, followed by post-hoc Tukey. The significance level established at p<0.05. Mean of oxygen saturation for the 112 molar dental pulps was 85.09%. There was no significant correlation (r=-0.007; p=0.977) between the mean of SaO2 of molar pulps with patient´s indicator finger (92.89%). There was a significant difference (p=0.037) between the mean of SaO2 of the first (85.76%) and second maxillary molars (81.87%), and it was not significant (p=0.1775) between the first and second mandibular molars. Maxillary molars had lower pulpal SaO2 (83.59%) than mandibular molars (86.89%) (p=0.018). The mean of the patient's response time to the cold stimulus was 1.12 s (maxillary molars 1.25 s and mandibular molars 0.99 s)(p=0.052). There was no significant correlation between the time response of the patient to the cold stimulus and the SaO2 for molars. The mean oxygen saturation level was 85.09%. The mandibular molars presented higher SaO2 level than maxillary molars.


Resumo Este estudo determinou o nível de saturação de oxigênio (SaO2) em polpas dentais hígidas de molares. O nível de SaO2 foi avaliado em 112 molares superiores e inferiores usando oxímetro de pulso. As variáveis quantitativas foram descritas pela média e desvio padrão. As variáveis com distribuição simétrica foram comparadas pelo teste t de Student e teste de Mann-Whitney. O coeficiente de correlação de Pearson foi utilizado para correlacionar variáveis quantitativas. A análise de variância foi utilizada para avaliar as diferenças nos níveis de SaO2 entre os grupos de molares, seguido de Tukey pós-hoc. A significância foi estabelecida em 0,05. O nível médio de SaO2 para as polpas de 112 molares foi de 85,09%, não havendo correlação com a média de SaO2 do dedo indicador do paciente (92,89%). Houve diferença significativa entre o nível médio de SaO2 dos primeiros molares superiores (85,76%) e os segundos molares superiores (81,87%) e não foi significativo entre os primeiros e os segundos molares inferiores. Os molares superiores apresentaram menor nível de SaO2 (83,59%) do que os molares inferiores (86,89%). A média do tempo de resposta do paciente ao estímulo com frio foi de 1,12 s (molares superiores 1,25 segundos e molares inferiores 0,99 segundos). Não houve correlação significativa entre o tempo de resposta do paciente ao estímulo com frio e o nível de saturação de oxigênio para os molares. Em resumo, o nível médio de saturação de oxigênio foi de 85,09%. Os molares inferiores apresentaram maior nível de SaO2 do que os molares superiors


Subject(s)
Humans , Male , Female , Adolescent , Adult , Young Adult , Oxygen/metabolism , Dental Pulp/metabolism , Mandible/metabolism , Maxilla/metabolism , Molar/metabolism
2.
Braz. dent. j ; 28(5): 573-577, Sept.-Oct. 2017. tab, graf
Article in English | LILACS | ID: biblio-888681

ABSTRACT

Abstract The aim of this study was to determine oxygen saturation levels in the dental pulp of maxillary premolars in different age groups. A total of 120 human maxillary premolars with normal dental pulps were selected covering the following age groups: 20-24, 25-29, 30-34, 35-39 and 40-44 years (n=24 each group). Oxygen saturation was assessed using pulse oximetry. Analysis of variance was used to assess differences in oxygen saturation levels and Tukey's test was used to identify the age groups that differed from each other. Significance was set at 0.05. Mean oxygen saturation of 120 premolars was 86.20% considering all age groups. Significantly reduced levels were found in the oldest group compared to the other groups: 40 to 44 years - 80.00% vs. 89.71, 87.67, 88.71, and 84.80% for age groups 20-24, 25-29, 30-34, 35-39 years, respectively. The mean oxygen saturation levels were similar between 20 and 39 years of age (86.20%) in the whole sample, but reduced significantly in the 40-44-year age group, suggesting that older patients present lower oxygen saturation results even in the absence of pulp tissue injury.


Resumo Este estudo determinou os níveis de saturação de oxigênio (SaO2) em polpas dentárias de pré-molares superiores em diferentes faixas etárias. Foram selecionados 120 pré-molares superiores humanos com polpas dentárias normais, abrangendo os seguintes grupos etários: 20-24, 25-29, 30-34, 35-39 e 40-44 anos (n=24 para cada grupo). A saturação de oxigênio foi avaliada utilizando oximetria de pulso. A análise de variância foi utilizada para avaliar diferenças nos níveis de saturação de oxigênio, e o teste de Tukey foi utilizado para identificar os grupos etários que diferiam uns dos outros. A significância foi estabelecida em 0,05. A saturação média de oxigênio foi de 86,20% considerando todos os grupos etários. Níveis significativamente reduzidos foram encontrados no grupo de indivíduos de maior idade em comparação aos outros grupos: 40 a 44 anos - 80,00% vs. 89,71, 87,67, 88,71 e 84,80% para os grupos etários 20-24, 25-29, 30-34, 35-39 anos. Os níveis médios de saturação de oxigênio foram semelhantes entre os 20 e os 39 anos de idade (86,20%), mas reduziram-se significativamente na faixa etária de 40-44 anos, sugerindo que os pacientes mais idosos apresentam menor saturação de oxigênio mesmo na ausência de lesão do tecido pulpar.


Subject(s)
Humans , Adult , Middle Aged , Young Adult , Oxygen/metabolism , Bicuspid/metabolism , Dental Pulp/metabolism , Maxilla/metabolism , Age Factors
3.
Actual. osteol ; 13(2): 104-115, Mayo - Ago. 2017. ilus, graf, tab
Article in Spanish | LILACS | ID: biblio-1117988

ABSTRACT

La osteonecrosis de maxilar asociada a aminobisfosfonatos (BRONJ) constituye un efecto secundario del tratamiento crónico con los más potentes. Un modelo experimental permitiría determinar la patogenia de dicha alteración. La oveja presenta características orales y del metabolismo óseo similar al humano y permite realizar manipulaciones bucales. Se evaluaron cambios clínicos, remodelación ósea y masa ósea maxilar en ovejas hembras adultas tratadas con zolendronato (ZOL), durante 22 meses y utilizando dosis equivalente al tratamiento de neoplasias. Seis ovariectomizadas (OVX) recibieron ZOL; 5 OVX y 4 SHAM (control) recibieron solución fisiológica. Al inicio, 4 y 22 meses se evaluó calcemia, fosfatemia, crosslaps (CTX) y fosfatasa alcalina ósea. Al final, se evaluó contenido mineral óseo de la hemimandíbula superior (CMO: mg/cm2). Al final del estudio, CTX disminuyó significativamente en ZOL (p<0,05) sin diferencias entre SHAM y OVX. En maxilar, los contenidos de Ca y P (g/g tejido) y CMO (g/cm2 ) disminuyeron en OVX vs. SHAM (p<0,05) y solo Ca y CMO respecto de ZOL (p<0,05). ZOL incrementó el contenido de Ca y CMO, mientras que el de P permaneció significativamente disminuido respecto de SHAM. La sobrevida en SHAM y OVX fue del 100% y en ZOL 77% (2 muertes); 2 ovejas del grupo ZOL presentaron necrosis de maxilar. Conclusiones: fue posible obtener desarrollo de BRONJ por tratamiento crónico con ZOL, el cual redujo notablemente la resorción y, según la relación Ca/P, posiblemente haya afectado la mineralización ósea. (AU)


Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a complication of chronic treatment with the most powerful aminobisphosphonates (BPs). An experimental animal model would allow to determine the pathogenesis of this complication. Ewes exhibit similar oral cavity characteristics and bone metabolism as humans, and they are suitable for oral cavity interventions. We examined herein the clinical manifestations, bone remodeling status, and maxillary bone mass in adult female ewes treated with zoledronate (ZOL) for 22 months. Six ovariectomized (OVX) ewes received ZOL; and 5 OVX and 4 SHAM animals received saline solution. At the start of the experiment, and at the 4 and 22 month-time points serum Ca, P, crosslaps (CTX), and bone alkaline phosphatase were measured. Bone mineral content (BMC) of the superior hemimandible was measured at the end of the experiment. At this time point, CTX was significantly decreased only in the ZOL group (p<0.05). Ca and P content (g/g tissue) and BMC in the mandible were significantly decreased in the OVX group compared to SHAM animals (p<0.05) and only Ca content and BMC were decreased when compared to ZOL (p<0.05). ZOL treatment increased the Ca content and BMC, whereas the P content remained low compared to the SHAM group (p<0.05). All ewes from the SHAM and OVX groups and 77% of the animals from the ZOL group survived until the end of the experiment, whereas two ewes of ZOL group exhibited BRONJ. Conclusion: under our experimental conditions, it was possible to induce BRONJ by the chronic ZOL administration, which in turn induced a high reduction in bone resorption as well as possibly impaired bone mineralization, based on the Ca/P ratio in the mandible. (AU)


Subject(s)
Animals , Diphosphonates/adverse effects , Bisphosphonate-Associated Osteonecrosis of the Jaw/pathology , Zoledronic Acid/adverse effects , Tooth Extraction , Bone Diseases, Metabolic/chemically induced , Sheep/metabolism , Sheep/blood , Biomarkers/blood , Bone Density/drug effects , Bone Remodeling/drug effects , Densitometry , Experimental Development , Bisphosphonate-Associated Osteonecrosis of the Jaw/etiology , Bisphosphonate-Associated Osteonecrosis of the Jaw/immunology , Bisphosphonate-Associated Osteonecrosis of the Jaw/prevention & control , Zoledronic Acid/administration & dosage , Glucocorticoids/therapeutic use , Analgesics/therapeutic use , Ilium/cytology , Anesthetics, Dissociative/therapeutic use , Lidocaine/therapeutic use , Maxilla/cytology , Maxilla/drug effects , Maxilla/metabolism , Maxilla/diagnostic imaging , Anti-Bacterial Agents/therapeutic use
4.
Braz. dent. j ; 28(3): 296-300, May-June 2017. graf
Article in English | LILACS | ID: biblio-888648

ABSTRACT

Abstract The aim of this study was to evaluate osteoclastogenesis signaling in midpalatal suture after rapid maxillary expansion (RME) in rats. Thirty male Wistar rats were randomly assigned to two groups with 15 animals each: control (C) and RME group. RME was performed by inserting a 1.5-mm-thick circular metal ring between the maxillary incisors. The animals were euthanized at 3, 7 and 10 days after RME. qRT-PCR was used to evaluate expression of Tnfsf11 (RANKL), Tnfrsf11a (RANK) and Tnfrsf11b (OPG). Data were submitted to statistical analysis using two-way ANOVA followed by Tukey test (a=0.05). There was an upregulation of RANK and RANKL genes at 7 and 10 days and an upregulation of the OPG gene at 3 and 7 days of healing. Interestingly, an increased in expression of all genes was observed over time in both RME and C groups. The RANKL/OPG ratio showed an increased signaling favoring bone resorption on RME compared to C at 3 and 7 days. Signaling against bone resorption was observed, as well as an upregulation of OPG gene expression in RME group, compared to C group at 10 days. The results of this study concluded that the RANK, RANK-L and OPG system participates in bone remodeling after RME.


Resumo O objetivo deste estudo foi avaliar a sinalização osteoclastogenese na sutura palatina após a expansão rápida da maxila (ERM) em ratos. Um total de 30 ratos Wistar machos foram divididos aleatoriamente em dois grupos com 15 animais cada: controle (C) e grupo ERM. ERM foi realizada através da inserção de um anel de metal circular de 1,5 mm de espessura entre os incisivos superiores. Os animais foram sacrificados aos 3, 7 e 10 dias após a RME. qRT-PCR foi utilizado para avaliar a expressão de Tnfsf11 (RANKL), Tnfrsf11a (RANK) e TNFRSF11b (OPG). Os dados foram submetidos à análise de variância de duas vias, seguido pelo teste de Tukey (a=0,05). Houve uma regulação positiva de genes RANK e RANKL aos 7 e 10 dias e uma regulação positiva do gene OPG aos 3 e 7 dias de tratamento. Curiosamente, foi observado um aumento na expressão de todos os genes ao longo do tempo nos grupos ERM e C. O RANKL/OPG mostrou um aumento na sinalização favorecendo a reabsorção óssea no ERM em comparação com o C nos períodos de 3 e 7 dias. Foi observada uma sinalização contra a reabsorção óssea, assim como, uma regulação favorável da expressão do gene OPG no grupo ERM, comparado ao grupo C aos 10 dias. Os resultados deste estudo permitem concluir que o sistema RANK, RANK-L e OPG participa de remodelação óssea após a ERM.


Subject(s)
Animals , Male , Maxilla/surgery , Osteogenesis , Osteoprotegerin/genetics , Palatal Expansion Technique/instrumentation , RANK Ligand/genetics , Receptor Activator of Nuclear Factor-kappa B/genetics , Bone Remodeling , Gene Expression , Maxilla/metabolism , Rats, Wistar , Real-Time Polymerase Chain Reaction , Signal Transduction , Up-Regulation , Wound Healing
5.
Biol. Res ; 47: 1-7, 2014. ilus, graf, tab
Article in English | LILACS | ID: biblio-950768

ABSTRACT

BACKGROUND: Acetylcholine (ACh) is known to be a key neurotransmitter in the central and peripheral nervous systems, which is also produced in a variety of non-neuronal tissues and cell. The existence of ACh in maxilla in vivo and potential regulation role for osteogenesis need further study. RESULTS: Components of the cholinergic system (ACh, esterase, choline acetyltransferase, high-affinity choline uptake, n- and mAChRs) were determined in maxilla of rat in vivo, by means of Real-Time PCR and immunohistochemistry. Results showed RNA for CarAT, carnitine/acylcarnitine translocase member 20 (Slc25a20), VAChT, OCTN2, OCT1, OCT3, organic cation transporter member 4 (Slc22a4), AChE, BChE, nAChR subunits α1, α2, α3, α5, α7, α10, ß1, ß2, ß4, γ and mAChR subunits M1, M2, M3, M4, M5 were detected in rat's maxilla. RNA of VAChT, AChE, nAChR subunits α2, ß1, ß4 and mAChR subunits M4 had abundant expression (2(-ΔCt) > 0.03). Immunohistochemical staining was conducted for ACh, VAChT, nAChRα7 and AChE. ACh was expressed in mesenchymal cells, chondroblast, bone and cartilage matrix and bone marrow cells, The VAChT expression was very extensively while ACh receptor α7 was strongly expressed in newly formed bone matrix of endochondral and bone marrow ossification, AchE was found only in mesenchymal stem cells, cartilage and bone marrow cells. CONCLUSIONS: ACh might exert its effect on the endochondral and bone marrow ossification, and bone matrix mineralization in maxilla.


Subject(s)
Animals , Male , Rats , Bone Marrow/physiology , Acetylcholine/metabolism , Cartilage/physiology , Cholinergic Agents/metabolism , Maxilla/metabolism , Osteogenesis/physiology , Bone Matrix/metabolism , Calcification, Physiologic/physiology , Bone Marrow Cells/metabolism , Immunohistochemistry , Carnitine Acyltransferases/genetics , Carnitine Acyltransferases/metabolism , Gene Expression Regulation/physiology , Receptors, Nicotinic/genetics , Rats, Sprague-Dawley , Organic Cation Transport Proteins/genetics , Organic Cation Transport Proteins/metabolism , Vesicular Acetylcholine Transport Proteins/genetics , Vesicular Acetylcholine Transport Proteins/metabolism , Mesenchymal Stem Cells/metabolism , Real-Time Polymerase Chain Reaction , Maxilla/cytology
6.
Braz. j. med. biol. res ; 44(7): 694-699, July 2011. ilus, tab
Article in English | LILACS | ID: lil-595703

ABSTRACT

The maxilla and masseter muscles are components of the stomatognathic system involved in chewing, which is frequently affected by physical forces such as gravity, and by dental, orthodontic and orthopedic procedures. Thyroid hormones (TH) are known to regulate the expression of genes that control bone mass and the oxidative properties of muscles; however, little is known about the effects of TH on the stomatognathic system. This study investigated this issue by evaluating: i) osteoprotegerin (OPG) and osteopontine (OPN) mRNA expression in the maxilla and ii) myoglobin (Mb) mRNA and protein expression, as well as fiber composition of the masseter. Male Wistar rats (~250 g) were divided into thyroidectomized (Tx) and sham-operated (SO) groups (N = 24/group) treated with T3 or saline (0.9 percent) for 15 days. Thyroidectomy increased OPG (~40 percent) and OPN (~75 percent) mRNA expression, while T3 treatment reduced OPG (~40 percent) and OPN (~75 percent) in Tx, and both (~50 percent) in SO rats. Masseter Mb mRNA expression and fiber type composition remained unchanged, despite the induction of hypo- and hyperthyroidism. However, Mb content was decreased in Tx rats even after T3 treatment. Since OPG and OPN are key proteins involved in the osteoclastogenesis inhibition and bone mineralization, respectively, and that Mb functions as a muscle store of O2 allowing muscles to be more resistant to fatigue, the present data indicate that TH also interfere with maxilla remodeling and the oxidative properties of the masseter, influencing the function of the stomatognathic system, which may require attention during dental, orthodontic and orthopedic procedures in patients with thyroid diseases.


Subject(s)
Animals , Male , Rats , Masseter Muscle/drug effects , Maxilla/drug effects , Myoglobin/metabolism , Osteopontin/metabolism , Osteoprotegerin/metabolism , Thyroid Hormones/physiology , Triiodothyronine/pharmacology , Blotting, Northern , Hyperthyroidism/physiopathology , Masseter Muscle/anatomy & histology , Masseter Muscle/metabolism , Maxilla/metabolism , Myoglobin/genetics , Osteopontin/genetics , Osteoprotegerin/genetics , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , RNA , RNA, Messenger/metabolism , Thyroidectomy , Thyroid Hormones/metabolism
7.
Braz. dent. j ; 21(3): 199-204, 2010. ilus, graf, tab
Article in English | LILACS | ID: lil-556817

ABSTRACT

Caffeine induces loss of calcium and influences the normal development of bone. This study investigated the effects of coffee on bone metabolism in rats by biochemical measurement of calcium, bone densitometry and histometry. Male rats, born of female treated daily with coffee and with coffee intake since born, were anesthetized, subjected to extraction of the upper right incisor, and sacrificed 7, 21 and 42 days after surgery. Blood and urine samples were taken, and their maxilla radiographed and processed to obtain 5-µm-thick semi-serial sections stained with hematoxylin and eosin. The volume and bone quality were estimated using an image-analysis software. The results showed significantly greater amount of calcium in the plasma (9.40 ± 1.73 versus 9.80 ± 2.05 mg percent) and urine (1.00 ± 0.50 versus 1.25 ± 0.70 mg/24 h) and significantly less amount in bone (90.0 ± 1.94 versus 86.0 ± 2.12 mg/mg bone), reduced bone mineral density (1.05 ± 0.11 versus 0.65 ± 0.15 mmAL), and lower amount of bone (76.19 ± 1.6 versus 53.41 ± 2.1 percent) (ANOVA; p≤0.01) in animals treated with coffee sacrificed after 42 days. It may be concluded that coffee/caffeine intake caused serious adverse effects on calcium metabolism in rats, including increased levels of calcium in the urine and plasma, decreased bone mineral density and lower volume of bone, thus delaying the bone repair process.


A cafeína induz perda de cálcio e influencia no desenvolvimento ósseo normal. Este estudo investiga os efeitos do café sobre o metabolismo ósseo em ratos através de avaliações bioquímicas do cálcio, densitometria e histometria óssea. Ratos machos, nascidos de fêmeas tratadas diariamente com café, e com ingestão de café desde o nascimento, foram anestesiados, submetidos à extração do incisivo superior direito e sacrificados 7, 21 e 42 dias após a cirurgia. Amostras de sangue e urina foram colhidas, suas maxilas radiografadas e processadas para se obter cortes semi seriados (5 µm) e corados pela hematoxilina-eosina. Através de um programa de análise de imagens, o volume e a qualidade do osso foram avaliados. Os resultados demonstraram maior quantidade de cálcio no sangue (9,40 ± 1,73 versus 9,80 ± 2,05 mg por cento) e urina (1,00 ± 0,50 versus 1,25 ± 0,70 mg/24 h) e menor no osso (90,0 ± 1,94 versus 86,0 ± 2,12 mg/mg osso), densidade mineral óssea menor (1,05 ± 0,11 versus 0,65 ± 0,15 mmAL), e menor quantidade de osso (76,19 ± 1,6 versus 53,41 ± 2,1 por cento) estatisticamente significante (ANOVA p≤0,01) nos animais tratados com café sacrificados após 42 dias. Conclui-se que a ingestão de café/cafeína causou sérios efeitos adversos no metabolismo de cálcio em ratos, incluindo aumento dos níveis de cálcio na urina e no plasma, diminuição da densidade mineral óssea e menor volume de osso atrasando o processo de reparo ósseo.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Bone Density/drug effects , Bone Remodeling/drug effects , Calcium/blood , Coffee/adverse effects , Maxilla/drug effects , Tooth Socket/drug effects , Coffee/metabolism , Maxilla/metabolism , Maxilla , Organ Size , Prenatal Exposure Delayed Effects , Rats, Wistar , Tooth Socket/metabolism , Wound Healing/drug effects , Wound Healing/physiology
8.
Bauru; s.n; 1988. 85 p. ilus, tab, graf.
Thesis in Portuguese | LILACS, BBO | ID: lil-250280

ABSTRACT

A análise morfológica do arco maxilar superior em fissurados transforame incisivo unilateral, operados, foi feita neste estudo, através do exame de 225 modelos de gesso do arco dentário superior de 40 pacientes do sexo masculino e 35 do sexo feminino, com idade variando de 3 a 9 anos, regularmente matriculados no Hospital de Pesquisa e Reabilitaçäo de Lesöes Lábio-Palatais da Universidade de Säo Paulo, em Bauru. Os pacientes foram divididos em dois grupos, o primeiro composto de pacientes submetidos a tratamento ortodôntico preventivo e o segundo de pacientes näo submetidos a tratamento ortodôntico preventivo. Todos os pacientes selecionados foram submetidos à cirurgia do lábio e do palato nos dois primeiros anos de vida. As cirurgias foram todas executadas por um único cirurgiäo e pela mesma técnica. Os modelos dos pacientes utilizados foram divididos de acordo com três fases representativas da evoluçäo do crescimento, considerando os grupos com e sem tratamento ortodôntico preventivo. Utilizando o método proposto por STOCKLI 1971 (70), foram demarcados nos modelos pontos de referência, utilizados para as dimensöes estudadas. Dos mesmos, obtivemos as cópias xerográficas e, através dos pontos demarcados, obtivemos os valores das distâncias utilizando um cursor de uma mesa digitalizadora acoplados e um microcomputador. Os resultados obtidos foram analisados estatisticamente e pudemos chegar às seguintes conclusöes...


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Cleft Lip/pathology , Cleft Palate/pathology , Dental Arch/anatomy & histology , Cleft Lip/surgery , Cleft Palate/surgery , Dental Arch/abnormalities , Dental Arch/metabolism , Longitudinal Studies , Mandible/abnormalities , Mandible/metabolism , Maxilla/abnormalities , Maxilla/metabolism , Maxillofacial Development
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