Curcumin Mediated Gold Nanoparticles and Analysis of its Antioxidant, Anti-inflammatory, Antimicrobial Activity Against Oral Pathogens

ABSTRACT Objective: To green synthesise gold nanoparticles using curcumin and to analyse its antioxidant, anti-inflammatory, and antimicrobial activity among oral pathogens. Material and Methods: Biosynthesised Curcumin Gold nanoparticles (CuAuNP) were evaluated by UV-visible spectrophotometer (UV-Vis), Transmission Electron Microscopy (TEM), and evaluation of antioxidant, anti-inflammatory and antibacterial activity against oral pathogens. Results: Synthesized CuAuNP were characterized using UV-visible spectrophotometry and showed peak absorption at 530nm. CuAuNp showed a 90.3% maximum scavenging ability of DPPH at a concentration of 50 μg/mL. CuAuNP exhibited 79.6 % of the highest anti-inflammatory activity at 50μg/mL than the standard drug diclofenac. TEM image clearly showed uniformly dispersed spherical-shaped gold nanoparticles with a size of about 20 nm. The biosynthesized nanoparticle was tested for its antimicrobial effect, and it showed a potent effect against S. aureus, E. faecalis, and C. albicans at 100µg/ mL. Enterococcus faecalis has a maximum zone of inhibition of 14 mm at 100µg/ mL of CuAuNp. Among gram-positive bacteria, a maximum zone of inhibition of 12 mm at 100µg/ mL was seen in S. aureus compared to S mutans. Candida albicans showed a maximum zone of inhibition of 18 mm at 25 μg/mL of CuAuNp. Conclusion: Curcumin-mediated gold nanoparticles with 20 nm size were effective and had strong antioxidant and anti-inflammatory activity at 50µg/ mL, antimicrobial action inhibiting microbes at 100µg/mL concentration that can be used in treating various Oral mucosal lesions.

The antioxidant activity of lemongrass leaves extract against fibroblasts oxidative stress / Atividade antioxidante do extrato das folhas de capim-limão contra o estresse oxidativo em fibroblastos

Objective : The purpose of this research is to assess the antioxidant activity of lemongrass leaves extract in terms of lowering ROS generation and its effect on the viability and proliferation of fibroblasts under oxidative stress. Material and Methods: The antioxidant activity was measured using the DPPH method and the ROS assay was carried out by fluorescent H2DCFDA staining. Viability and proliferation assays were performed using the Cell Counting Kit-8 (CCK-8) and was read at 450 nm using microplate reader. The groups were divided into 8, namely fibroblasts without treatment (comparison group), fibroblast induced by H2O2 (negative control), fibroblast with H2O2 then treated with ascorbic acid (positive control), and fibroblast with H2O2 then treated with lemongrass leaves extract at various concentrations (10, 20, 30, 40, and 50 ppm). Results: The results showed that the antioxidant activity of lemongrass leaves extract had an IC value of 64.17 ppm. ROS production were reduced by the LgLE of all concentrations if compared with negative control (p=0.819). LgLE can maintained the fibroblast viability with 10 ppm of LgLE was the most optimum concentration (p<0.05). LgLE can induced the proliferation of fibroblast, with the most effective was at 24 h of observation (p<0.05). Conclusion: Lemongrass leaves extract has a strong antioxidant activity that can reduce oxidative stress and increase the viability and proliferation of fibroblasts with the optimum concentration is at 10 ppm. (AU)

Objetivo: O intuito deste estudo foi determinar a ação antioxidante do extrato das folhas de capim-limão no que se refere a diminuição da produção de espécies reativas do oxigênio (EROS) e o seu efeito na viabilidade e proliferação de fibroblastos submetidos à estresse oxidativo. Material e Métodos: A atividade antioxidante foi medida utilizando o método de DPPH e o ensaio de EROS foi realizado pela coloração fluorescente de H2DCFDA. Os ensaios de proliferação e viabilidade foram realizados utilizando-se o kit de contagem de células CCK-8 em microplacas de leitura à 450nm. Os grupos foram divididos em 8: Fibroblastos sem tratamento (grupo controle), Fibroblastos tratados com H2O2 (controle negativo), Fibroblastos tratados com H2O2 e extrato da folha de capim-limão em concentrações variadas (10, 20, 30, 40 e 50 ppm). Resultados: Os resultados mostraram que a atividade antioxidante do extrato de capim-limão teve uma IC50 (com o numeroal subscrito) com valor de 64.17ppm. A produção de ROS foi reduzida pelo tratamento com o extrato em todas as concentrações testadas quando comparado ao grupo controle negativo (p=0.819). O extrato manteve a viabilidade dos fibroblastos, sendo 10ppm a concentração menos tóxica (p<0.05). LgLE pôde induzir a proliferação de fibroblastos, sendo que a melhor eficiencia foi após 24h de observação (p<0.05). Conclusão: O extrato das folhas de capim-limão apresentam forte atividade antioxidante reduzindo o estresse oxidativo e aumentando a viabilidade e proliferação de fibroblastos, sendo a concentração ótima de 10ppm. (AU)

Effect antioxidants application on microshear bond strength of universal adhesive to bleached enamel / Efeito da aplicação de antioxidantes na resistência de união do adesivo universal ao esmalte clareado

Purpose: To evaluate, in vitro, the influence of antioxidants (green tea extract - GT and sodium ascorbate - SA) on microshear bond strength (µSBS) of a universal adhesive system ­ self-etching mode (UAS) to bleached enamel. Material and Methods: After obtaining 50 fragments of human dental enamel (4 mm x 4 mm), forty fragments were submitted to at-home bleaching technique using 10% carbamide peroxide (Opalescence PF, Ultradent) for two h/day, for four weeks. They were randomly divided in four groups (n = 10): GT - 10% aqueous GT solution (60 min); SA - 10% SA solution (10 min); Negative control - no antioxidant agent, immediately restored; PC1 (positive control 1) - no antioxidant agent, restored 14 days the bleaching procedure. Ten enamel fragments were assigned to PC2 group (positive control 2), in which the adhesive procedures were realized in non-bleached enamel. The UAS (Adper Single Bond Universal, 3M ESPE) was applied on enamel surface according to manufacturer's instructions and two cylinders (0.8 mm diameter) of nanoparticulate composite resin (Z350, 3M ESPE) were made on each sample. After 24 h, the cylinders were submitted to µSBS in a universal test machine (0.5 mm/min). Fracture mode was evaluated in stereomicroscope (30x magnification). SBS data, in MPa, was submitted to one-way ANOVA and fracture mode to Chi-square test (α = 0.05). Results: There was no statistical difference between the experimental groups (p = 0.545) and fracture mode (p = 0.16424). There was predominance of adhesive fracture in all groups. Conclusion: Neither the bleaching procedure nor the application of antioxidants to bleached enamel interfered in the bond strength of the tested universal adhesive system (AU)

Objetivo: Avaliar, in vitro, a influência de antioxidantes (extrato de chá verde - GT e ascorbato de sódio - SA) na resistência de união ao microcisalhamento (µSBS) de um sistema adesivo universal - modo de autocondicionamento (UAS) ao esmalte clareado. Material e Métodos: Realizou-se a obtenção de 50 fragmentos de esmalte dental humano (4 mm x 4 mm), sendo que desses, quarenta fragmentos foram submetidos à técnica de clareamento caseiro utilizando peróxido de carbamida a 10% (Opalescence PF, Ultradent) por duas horas/dia, durante quatro semanas. Eles foram divididos aleatoriamente em quatro grupos (n= 10): Expostos a GT - solução aquosa de GT a 10% (60 min); expostos a SA - solução 10% SA (10 minutos); Sem exposição ao agente antioxidante e imediatamente restaurado - (controle negativo); Sem exposição ao agente antioxidante e restaurado 14 dias após o clareamento - PC1 (controle positivo 1). Os dez fragmentos de esmalte restantes foram atribuídos ao grupo PC2 (controle positivo 2), no qual os procedimentos adesivos foram realizados em esmalte não clareado. O UAS (Adper Single Bond Universal, 3M ESPE) foi aplicado na superfície do esmalte de acordo com as instruções do fabricante e dois cilindros (0,8 mm de diâmetro) de resina composta nanoparticulada (Z350, 3M ESPE) foram feitos em cada amostra. Após 24 h, os cilindros foram submetidos ao µSBS em uma máquina de teste universal (0,5 mm/min). O modulo de fratura foi avaliado em estereomicroscópio (aumento de 30x). Os dados do SBS, em MPa, foram submetidos à ANOVA unidirecional e ao modo fratura ao teste do qui-quadrado (α = 0,05). Resultados: Não houve diferença estatística entre os grupos experimentais (p = 0,545) e modulo de fratura (p = 0,16424). Houve predomínio de fratura adesiva em todos os grupos. Conclusão: Nem o procedimento de clareamento nem a aplicação de antioxidantes no esmalte clareado interferiram na resistência de união do sistema adesivo universal testado. (AU)

Comparison of total antioxidant capacity of saliva in men based on daily cigarette consumption / Comparação da capacidade antioxidante total da saliva em homens com base no consumo diário de cigarros

Objectives: Antioxidants play an important role in neutralizing of destructive effects of free oxygen and nitrogen radicals. There are contradictory results regarding the relationship between cigarette smoking and total antioxidant capacity of saliva. In this study, the total antioxidant capacity of saliva has been compared in normal smokers, heavy smokers and non-smokers. Material and methods: In this cross-sectional study, 28 heavy male smokers (more than one pack of cigarettes per day), 28 normal male smokers (less than one pack of cigarettes per day), and 28 male non-smokers aged 25 to 40 years old entered the study. Unstimulated saliva was collected by Spitting method. The total antioxidant capacity of saliva was measured using Ferric Reducing Antioxidant Power Assay. Descriptive statistics, ANOVA, and Tukey tests were used to analyze the data. Results: The mean total antioxidant capacity of saliva in male non-smokers was 0.0598 ± 0.08 µmol / L, in normal male smokers was 0.049 ± 0.04 µmol / L, and in heavy male smokers was 0.0388 ± 0.035 µmol / L, which did not show any significant difference between the groups (P > 0.05). Conclusion: The results of this study indicate that smoking does not have a significant effect on total antioxidant capacity of saliva in smokers (AU)

Objetivos: Os antioxidantes desempenham um papel importante na neutralização dos efeitos destrutivos do oxigênio livre e dos radicais de nitrogênio. Existem resultados contraditórios entre a relação do tabagismo e a capacidade antioxidante total da saliva. Neste estudo, a capacidade antioxidante total da saliva foi comparada em fumantes normais, fumantes pesados e não fumantes. Material e métodos: Neste estudo transversal, 28 fumantes pesados (mais de um maço de cigarros por dia), 28 fumantes normais (menos de um maço de cigarros por dia) e 28 homens não fumantes com idade entre 25 e 40 anos de idade foram incluídos no estudo. A saliva não estimulada foi coletada pelo método Spitting. A capacidade antioxidante total da saliva foi medida usando o ensaio de poder antioxidante redutor férrico. Estatística descritiva, ANOVA e testes de Tukey foram usados para analise dos dados.Resultados: A capacidade antioxidante total média da saliva em não fumantes do sexo masculino foi de 0,0598 ± 0,08 µmol / L, em fumantes normais do sexo masculino foi de 0,049 ± 0,04 µmol / L, e em fumantes pesados do sexo masculino foi de 0,0388 ± 0,035 µmol / L, e não foi observada diferença significativa entre os grupos (P> 0,05). Conclusão: Os resultados deste estudo indicaram que o tabagismo não tem efeito significativo na capacidade antioxidante total da saliva em fumantes (AU)

Effect of antioxidant agents after dental bleaching on luting of ceramic laminates / Efeito de agentes antioxidantes pós-clareamento na cimentação de laminados cerâmicos

O objetivo deste estudo in vitro foi avaliar o efeito da aplicação de agentes antioxidantes após o clareamento dentário e previamente à cimentação de laminados cerâmicos na estabilidade cromática do conjunto restaurador, assim como nas propriedades mecânicas de nanodureza (HIT), módulo de elasticidade (Eit*), grau de conversão, resistência de união e morfologia da interface adesiva. Ademais, a neutralização de peróxido de hidrogênio e a caracterização superficial do esmalte, como ângulo de contato, energia de superfície, energia livre total de interação, microscopia eletrônica de varredura e espectroscopia de energia dispersiva do substrato submetido à ação das soluções antioxidantes e do agente clareador também foram analisados. Duzentos e quarenta e dois blocos de esmalte dentário (7x8x0,6mm) foram utilizados para o processo de cimentação e distribuídos em grupos experimentais de acordo com os métodos de procedimentos (grupo não clareado, grupo clareado com Whiteness HP Maxx 35%), tipos de antioxidantes adotados (controle; ácido ascórbico 10% e α-tocoferol 10%) e períodos de cimentação (após 24 horas e 14 dias do processo de cimentação) (n = 22). Foi utilizado o sistema adesivo Tetric N Bond Universal e o cimento resinoso Variolink Esthetic LC (Ivoclar Vivadent) como agentes cimentantes. Os dados foram submetidos a testes estatísticos de normalidade e analisados por ANOVA e teste de Tukey (α = 0,05). Os dados da morfologia da interface adesiva, obtidas pela microscopia confocal a laser, foram submetidas ao teste Kappa inter-examinadores e os dados foram submetidos aos testes Kruskal-Wallis e Dunn (α = 0,05). Os resultados mostraram que, de modo geral, a utilização da solução antioxidante α-tocoferol 10% pós-clareamento no período mediato promoveu resultados satisfatórios com relação à estabilidade cromática do conjunto restaurador, assim como para as propriedades mecânicas, grau de conversão, resistência de união e morfologia da interface adesiva comparado ao grupo clareado sem associação dos agentes antioxidantes, tanto para o período mediato, quanto para o período de 14 dias (p< 0,05). A solução de αtocoferol 10% apresentou maiores valores de neutralização do peróxido de hidrogênio e maiores valores de molhabilidade do esmalte em relação aos grupos controle e ácido ascórbico (p< 0,05). A energia de superfície e energia livre total de interação do esmalte dentário foi significativamente influenciada pelo tratamento clareador (p< 0,05). Dessa forma, conclui-se que o emprego da solução antioxidante α-tocoferol 10% promoveu resultados promissores, sugerindo que o mesmo poderia ser utilizado mediatamente após o clareamento dental na cimentação de laminados cerâmicos(AU)

The aim of this in vitro study was to evaluate the effect of antioxidant agents application after tooth bleaching and prior to luting of ceramic veneers on color stability of the restorative set, as well as on mechanical properties of nanohardness (HIT), elastic modulus (Eit*), degree of conversion, bond strength and morphology of the adhesive interface. Furthermore, the hydrogen peroxide neutralization and surface characterization of enamel, such as contact angle, surface energy, total free energy of interaction, scanning electron microscopy and energy-dispersive spectroscopy of the substrate submitted to the action of antioxidant solutions and bleaching agent were also analyzed. Two hundred forty two dental enamel blocks (7 x 8 x 0.6 mm) were used for the luting process and distributed into experimental groups according to the procedure methods (unbleached group, bleached group with Whiteness HP Maxx 35%), types of antioxidants adopted (control; 10% ascorbic acid and 10% α-tocopherol) and the luting periods (24 hours and 14 days after the luting process) (n = 22). Tetric N Bond Universal adhesive system and Variolink Esthetic LC resin cement (Ivoclar Vivadent) were used as luting agents. Data were submitted to statistical tests of normality and analyzed by ANOVA and Tukey tests (α = 0.05). The adhesive interface morphology data, obtained by confocal laser microscopy, were submitted to the interexaminer Kappa test and the data were submitted to Kruskal-Wallis and Dunn´s tests (α = 0.05). The results showed that, in general, the use of 10% α-tocopherol antioxidant solution after bleaching in mediate period promoted satisfactory results regarding the color stability of the restorative set, as well as for the mechanical properties, degree of conversion, shear bond strength and adhesive interface morphology compared to the bleached group without antioxidant agents association, both for the mediate and 14-day period (P < 0.05). The 10% αtocopherol solution showed higher hydrogen peroxide neutralization values and higher enamel wettability values compared to the control and ascorbic acid groups (P < 0.05). Surface energy and total free energy of interaction of tooth enamel were significantly influenced by the bleaching treatment (P < 0.05). Thus, it is concluded that the use of 10% αtocopherol antioxidant solution promoted promising results, suggesting that it could be used mediately after tooth bleaching on luting of ceramic laminates(AU)

Os efeitos da Punica granatum L. em diferentes concentrações sobre duas linhagens celulares: estudo in vitro / The effects of Punica granatum L. at different concentrations on two cell lines: in vitro study

Introdução: A Punica granatum L. (PG), utilizada como medicamento fitoterápico, apresenta propriedades terapêuticas, anti-inflamatórias e antioxidante. Embora diversos estudos já tenham sido realizados com este fitoterápico, seus possíveis efeitos citotóxicos nos tecidos humanos ainda não são claros. Objetivo: Avaliar a citotoxicidade da PG por meio de cultura celular com duas linhagens: fibroblastos humanos de mucosa oral (FLM) e células de carcinoma epidermoide oral humano (KB). Material e método: As células foram submetidas ao teste de viabilidade celular por 24 horas nas concentrações da PG 1%, 0,50%, 0,25%, 0,125%, 0,062% e 0,031%, e aos testes de citotoxicidade celular em 4 horas, 1, 3, 5 e 7 dias, em diferentes concentrações, realizados em triplicata. Foi utilizado um controle negativo (Triton 1%) e um controle positivo sem o extrato de PG. Os dados obtidos foram submetidos à ANOVA (p < 0,05). Resultado: Foi possível observar que o extrato da PG possui efeitos inibitórios, apresentando-se maior nas células KB em relação às FLM. Os testes de citotoxicidade e viabilidade mostraram inibição e morte das células KB e FLM nas concentrações 1%, 0,50% e 0,25%. Conclusão: O efeito inibitório da PG foi dose-dependentes, mostrando-se maior nas células KB em relação às FLM.

Introduction: Punica granatum L. (PG), used as a herbal medicine, has therapeutic, anti-inflammatory and antioxidant properties, although several studies have already been carried out with this herbal medicine, its possible cytotoxic effects on human tissues are still unclear. Objective: To evaluate the cytotoxicity of PG through cell culture with two strains: human oral mucosa fibroblasts (LFM) and human oral squamous cell carcinoma (KB) cells. Material and method: The cells were submitted to the cell viability test for 24 hours in the concentrations of PG 1%, 0.50%, 0.25%, 0.125%, 0.062% and 0.031% and the cell cytotoxicity tests in 4 hours, 1, 3, 5 and 7 days in different concentrations, performed in triplicate. A negative control (Triton 1%) and a positive control without the PG extract were used. The data obtained were submitted to ANOVA (p <0.05). Result: it was possible to observe that the PG extract has inhibitory effects, being higher in KB cells in relation to LFM. The cytotoxicity and viability tests showed inhibition and death of KB and FLM cells at concentrations of 1%, 0.50% and 0.25%. Conclusion: The inhibitory effect of PG was dose dependent, showing itself to be greater in KB cells compared to LMB.

A via Nrf2 participa da maior modulação endotelial induzida pela prenhez sobre reatividade de aortas à fenilefrina / The Nrf2 pathway participates in the greater endothelial modulation induced by pregnancy on reactivity of aortas to phenylephrine

Alterações em diferentes vias de sinalização levam a disfunção vascular e endotelial e consequentemente a hipertensão. A hipertensão está relacionada diretamente com o aumento da produção de espécies reativas de oxigênio (ROS) e diminuição da biodisponibilidade de óxido nítrico (NO) nos vasos sanguíneos. A via do Nrf2 (fator nuclear eritróide 2) está envolvida nos mecanismos que levam ao aumento da biodisponibilidade vascular de NO, pois controla a expressão de enzimas antioxidantes. A ativação do Nrf2 é modulada por sua ligação com a Keap-1 (Kelch-like ECH-associated protein 1) e sua atividade é modulada pelo fator de transcrição Bach-1, que compete pelo mesmo sitio ativo no DNA com o Nrf2. Em ratas normotensas e em ratas espontaneamente hipertensas (SHR) é observada uma redução da pressão arterial ao final da prenhez, que tem sido associada à redução do estresse oxidativo e maior biodisponibilidade de NO. Com o aumento da biodisponibilidade de NO, é aumentada a modulação do endotélio sobre a reatividade vascular à agonistas vasoconstritores, como à fenilefrina (PE). Levantamos a hipótese que a prenhez altera a expressão e ou a atividade do Nrf2 e de seus inibidores Keap-1 e Bach-1 e que estas possíveis alterações estariam associadas à maior modulação endotelial sobre contração de aortas à PE. Para testarmos esta hipótese, a expressão de Nrf2, Keap-1 e Bach-1 e também das enzimas antioxidantes transcritas pelo Nrf2, como a NADP(H) quinona oxirredutase-1 (NQO1), SOD-1 e SOD-2 foram avaliadas em aortas de ratas prenhes e comparadas as aortas de ratas não-prenhes. A fim de identificarmos outros possíveis mecanismos alterados pela prenhez em ratas Wistar e SHR, avaliamos a expressão de NOXO-1, subunidade regulatória da NOX1 e de p47phox, subunidade regulatória de NOX2. A participação do Nrf2 na produção de NO endotelial em aortas de ratas prenhes, foi avaliada pela utilização de Brusatol, uma droga inibidora do Nrf2. Avaliamos também a participação do Nrf2 na reatividade de aortas de ratas prenhes à fenilefrina e à acetilcolina, utilizando o Brusatol. Todos os resultados foram comparados entre ratas não-prenhes normotensas (Wistar) e hipertensas (SHR) e entre ratas não-prenhes e prenhes nos grupos (análise de multivariância, post-test Tukey, p< 0,05). Os resultados mostraram que a expressão de Nrf2 está aumentada em aortas de ratas prenhes Wistar, apesar da expressão de Keap-1 e de Bach1 não estar alterada. Associado a expressão aumentada de Nrf2 observamos maior expressão de SOD-2, mas não de SOD-1 ou NQO1, em aortas de ratas prenhes. Em aortas de ratas SHR não prenhes, observamos entre todas as proteínas avaliadas, menor expressão de Bach-1 e de NQO1 quando comparadas às aortas de ratas normotensas. A prenhez reduziu ainda mais a expressão apenas de NQO1 em aortas de SHR. A prenhez reduziu a expressão de NOXO-1 e de p47phox em aortas de SHR, enquanto que em aortas de ratas Wistar reduziu apenas a expressão de NOXO-1. Os resultados obtidos neste estudo mostraram também que a incubação de HUVEC com Brusatol aumentou as concentrações intracelulares de ERO, mas não alterou as concentrações de NO, no entanto, reduziu significativamente a concentração de NOx estimulada pela ACh em aortas de ratas prenhes, Wistar ou SHR. Além disto, o Brusatol aumentou a reatividade à PE em aortas de ratas normotensas não prenhes e prenhes, igualando a reatividade de aortas de ratas prenhes as aortas de ratas não prenhes. No entanto, o Brusatol não alterou a reatividade de aortas de SHR, prenhes ou não-prenhes. Nenhum efeito significativo do Brusatol foi observado na reatividade à Acetilcolina em aortas de ratas Wistar ou SHR, prenhes ou não prenhes. Em conclusão, nossos resultados sugerem que a atividade da via de sinalização do Nrf2 está aumentada, favorecendo a maior atividade de enzimas antioxidantes como a SOD-2, que contribuiria para maior biodisponibilidade de NO e maior modulação endotélio-dependente da contração vascular à PE em aortas de ratas normotensas prenhes. No entanto, em aortas de SHR prenhes, este mecanismo parecer não ser mais importante que a redução da atividade de isoformas NOX e de suas subunidades regulatórias que contribuiria para menor geração de O2•- e consequentemente, maior biodisponibilidade de NO(AU)

Modifications in different signaling pathways lead to vascular and endothelial dysfunction and, consequently, hypertension. Hypertension is directly related to an increase in the production of reactive oxygen species (ROS) and a decrease in the bioavailability of nitric oxide (NO) in blood vessels. The Nrf2 (erythroid nuclear factor 2) pathway is involved in the mechanisms that lead to the increased vascular bioavailability of NO, as it controls the expression of antioxidant enzymes. The activation of Nrf2 is modulated by Keap-1 (Kelch-like ECH-associated protein 1) and its activity is modulated by the transcription factor Bach-1, which competes for the same active site in DNA with Nrf2. In normotensive rats and spontaneously hypertensive rats (SHR), a reduction in blood pressure at the end of pregnancy is observed, which has been associated with a reduction in oxidative stress and greater bioavailability of NO. This increased NO bioavailability has been associated with the higher endothelium modulation over blood vessel reactivity to vasoconstrictor agonists, such as phenylephrine (PE), observed in pregnant rats. We hypothesized that pregnancy alters the expression and/or activity of Nrf2 and its inhibitors Keap-1 and Bach-1 and that these changes are associated with greater endothelial modulation on the contraction of aortas to PE. To test this hypothesis, the expression of Nrf2, Keap-1 and Bach-1 and the antioxidant enzymes transcribed by Nrf2, such as NADP (H) quinone oxidoreductase-1 (NQO1), SOD-1 and SOD-2 were evaluated in aortas of pregnant rats and compared to aortas of non-pregnant rats. In order to identify other possible mechanisms altered by pregnancy in Wistar rats and SHR, we evaluated the expression of NOXO-1, NOX1 regulatory subunit and p47phox, NOX2 regulatory subunit. The role of Nrf2 in the production of endothelial NO in aortas of pregnant rats was evaluated by use of Brusatol, an inhibitor of Nrf2. We also evaluated the role of Nrf2 in the reactivity of aortas of pregnant rats to phenylephrine and acetylcholine, using Brusatol. All results were compared between normotensive (Wistar) and hypertensive (SHR) non-pregnant rats and between pregnant and non-pregnant rats in the groups (multivariate analysis, Tukey post-test, p< 0.05). The results showed that the expression of Nrf2 is increased in aortas of pregnant Wistar rats, although the expression of Keap-1 and Bach-1 is not altered. The increased expression of Nrf2 was associated with the greater expression of SOD-2, but not of SOD-1 or NQO1, in aortas of pregnant rats. In aortas of non-pregnant SHR rats, we observed among all evaluated proteins, lower expression of Bach-1 and NQO1 when compared to the aortas of normotensive rats. Pregnancy reduced even more the expression of NQO1 in SHR aortas. Pregnancy reduced the expression of NOXO-1 and p47phox in SHR aortas, whereas in aorta of Wistar rats it reduced only the expression of NOXO-1. The results obtained in this study also showed that the incubation of HUVEC with Brusatol increased the intracellular concentrations of ROS, but did not alter the concentrations of NO, however, Brusatol significantly reduced the concentration of NOx stimulated by ACh in aortas of pregnant rats, Wistar or SHR. Moreover, Brusatol increased the reactivity to PE in aortas of pregnant normotensive rats and pregnant, matching the reactivity of aortas of pregnant rats to aortas of non-pregnant rats. However, Brusatol did not alter the reactivity of pregnant or non-pregnant SHR aortas. No significant effect of Brusatol was observed in the reactivity to Acetylcholine in aortas of Wistar rats or SHR, pregnant or non-pregnant rats. In conclusion, our results suggest that the activity of the Nrf2 signaling pathway is increased, favoring the greater activity of antioxidant enzymes such as SOD-2, which would contribute to greater bioavailability of NO and greater endothelium-dependent modulation of vascular contraction to PE in aortas of pregnant normotensive rats. However, in pregnant SHR aortas, this mechanism appears to be no more important than the lower the activity of NOX isoforms and their regulatory subunits that would contribute to lower O2•- generation and, consequently, greater NO bioavailability(AU)

Impacto da orquiectomia e terapia de reposição hormonal com cipionato de testosterona no estresse oxidativo e função secretora das glândulas salivares de ratos Wistar / Impact of orchiectomy and cypionate testosterone replacement on stress oxidative and salivary gland function in Wistar rats

Apesar da comprovada capacidade da testosterona (T) em modular o estresse oxidativo de forma tecido-específica, pouco se sabe se as glândulas salivares estão sujeitas a essa modulação. O objetivo foi investigar os efeitos da orquiectomia (OQX) e da terapiadereposiçãohormonal(TRH) comTnoestresse oxidativoefunçãosecretora das glândulas salivares. Ratos Wistar (3 meses de idade) foram randomizados em 3 grupos (n = 15 ratos/grupo): simulação de cirurgia (SHAM); OQX; e OQX tratado com cipionato de testosterona (CT). A TRH com T foi realizada por via intramuscular, semanalmente, com 10 mg/kg de massa corpórea de CT por 4 semanas, iniciando 4 semanas após a OQX. Após o tratamento, o fluxo salivar (FS) induzido por pilocarpina foi coletada e as glândulas parótidas (PA) e submandibulares (SM) foram armazenadas a -80 ºC e submetidas a posteriores análises bioquímicas e histomorformétricas. O FS e as concentrações de cálcio, fosfato e cloreto aumentaram no grupo OQX. Após a OQX diminuíram a proteína total (PT) e a atividade da amilase (AMI), enquanto não houve nenhuma alteração na capacidade tamponante, pH, sódio e potássio na saliva. A concentração de PT e atividade de AMI aumentaram no grupo CT, enquanto que as concentraçoes de fosfato e cálcio reduziram na saliva em comparação com o grupo OQX. Proteína carbonilada, substâncias reativas ao ácido tiobarbitúrico, capacidade antioxidante total, ácido úrico e glutationa total aumentaram no grupo OQX em ambas as glândulas salivares. Superóxido dismutase, catalase e glutationa peroxidase aumentaram após a OQX na glândula SM, porém nenhuma alteração nas enzimas antioxidantes foi observada na glândula PA. A área ductal e acinar diminuiram e a área de tecido conjuntivo aumentou na glândula PA após a OQX. A área ductal diminuiu e a área acinar aumentou na SM, entretanto, não houve alteração na área de tecido conjuntivo após a OQX. A TRH com CT restaurou todos os parâmetros para níveis próximos ao grupo SHAM. Conclui-se que a OQX modula o estresse oxidativo nas glândulas salivares, e pode afetar a secreção e composição da saliva(AU)

Despite the proven ability of testosterone (T) to modulate oxidative stress in a tissuespecific manner, little is known whether the salivary glands are subject to this modulation. The objective was to investigate the effects of orchiectomy (ORX) and hormone replacement therapy (HRT) with T on oxidative stress and secretory function of the salivary glands. Wistar rats (3 months old) were randomized into 3 groups (n = 15 rats / group): surgery simulation (SHAM); ORX; and ORX treated with testosterone cypionate (TC). HRT with T was performed intramuscularly (I.M.), weekly, with 10 mg/kg body weight of TC for 4 weeks, starting 4 weeks after ORX. After treatment, the salivary flow (FS) induced by pilocarpine was collected and the parotid (PA) and submandibular (SM) glands were stored at -80 °C and subjected to subsequent biochemical and histomorformetric analyzes. FS and calcium, phosphate and chloride concentrations increased in the ORX group. After ORX, total protein (TP) and amylase activity (AMY) decreased, while there was no change in buffering capacity, pH, sodium and potassium in saliva. The TP concentration and AMY activity increased in the TC group, while the phosphate and calcium concentrations decreased in saliva compared to the ORX group. Carbonylated protein, thiobarbituric acid reactive substances, total antioxidant capacity, uric acid and total glutathione increased in the ORX group in both salivary glands. Superoxide dismutase, catalase and glutathione peroxidase increased after ORX in the SM gland, but no changes in antioxidant enzymes were observed in the PA gland. The ductal and acinar area decreased and the area of connective tissue increased in the PA gland after ORX. The ductal area decreased and the acinar area increased in SM, however, there was no change in the connective tissue area after ORX. HRT with TC restored all parameters to levels close to the SHAM group. It is concluded that ORX modulates oxidative stress in the salivary glands, and can affect the secretion and composition of saliva(AU)

High Mobility Group Box 1 and Heat Shock Protein-70 Expression Post (-)-Epigallocatechin-3-Gallate in East Java Green Tea Methanolic Extract Administration During Orthodontic Tooth Movement in Wistar Rats

Abstract Objective: To investigate the expression of High Mobility Group Box 1 (HMGB1) and Heat Shock Protein-70 (HSP-70) during orthodontic tooth movement (OTM) after (-)- Epigallocatechin-3-Gallate (EGCG) in East Java Green Tea (Camelia Sinensis) Methanolic Extract (GTME) administration in vivo. Material and Methods: 28 Wistar rats (Rattus Novergicus) was used and divided into 4 groups accordingly: K- without EGCG and OTM; K+ with OTM, without EGCG for 14 days; T1with OTM for 14 days and EGCG for 7 days; treatment group 2 (T2) with OTM and EGCG for 14 days. OTM animal model was achieved through the installation of the OTM device by means of NiTi close coil spring with 10g force placed between the first incisor and first maxillary molars. The samples were terminated on Day 14. The pre-maxillary was isolated for the immunohistochemical examination. Analysis of Variance (ANOVA) then continued with Tukey Honest Significant Difference (HSD) (p<0.05) was performed to analyze the data. Results: The highest HMGB1 and HSP-70 expression were found in the K+ group pressure side, meanwhile the lowest HMGB1 and HSP-70 expression were found in K- group tension side in the alveolar bone. There was a significant decrease of HMGB1 and HSP-70 expression in T2 compared to T1 and K+ with significant between groups (p<0.05; p=0.0001). Conclusion: The decreased expression of HMGB1 and HSP-70 in alveolar bone of OTM wistar rats due to post administration of GTME that consisted EGCG.

Analysis of the Total Antioxidant Capacity of Saliva in Smokers

Objective: To analyze the total antioxidant capacity (TAoC) of saliva in smokers based on type of cigarette, duration and frequency of smoking. Material and Methods: 51 male smokers, aged 20-55 years were enrolled. Information regarding cigarette type and smoking duration and frequency was collected using a questionnaire. Unstimulated saliva samples were collected in the morning following fasting for 2 h, and TAoC was measured using a commercial kit. The data were evaluated through the independent t-test and Kruskal-Wallis test. Results: Mean TAoC for the consumption of Kretek cigarettes was 0.29 (±0.15) and for that of non-Kretek cigarettes was 0.36 (±0.10). Mean TAoC based on smoking duration was 0.31 (±0.14) for 5-10 years and 0.27 (±0.15) for >10 years. Median TAoC based on smoking frequency was 0.23 (0.11-0.44), 0.31 (0.06-0.64), and 0.27 (0.06-0.68) for 1-5, 6-10, and 11-20 cigarettes/day. Mean TAoC of the saliva from participants who consumed Kretek cigarettes was lower than that of the saliva from those who consumed non-Kretek cigarettes (p=0.3). Mean TAoC for a duration >10 years was lower than that for a duration of 5-10 years, although the difference between these two groups was not significant (p=0.4). Conclusion: There were tendencies of lower total antioxidant capacity on smokers with kretek type cigarettes, smoking duration >10 years and frequency of 1-5 cigarettes/day. This study indicates that the type, duration, and frequency of smoking may affect the salivary total antioxidant capacity.

Gliclazide reduced oxidative stress, inflammation, and bone loss in an experimental periodontal disease model

Abstract Objective The aim of this study was to evaluate the effects of gliclazide on oxidative stress, inflammation, and bone loss in an experimental periodontal disease model. Material and Methods Male albino Wistar rats were divided into no ligature, ligature, and ligature with 1, 5, and 10 mg/kg gliclazide groups. Maxillae were fixed and scanned using micro-computed tomography to quantify linear and bone volume/tissue volume (BV/TV) and volumetric bone loss. Histopathological, immunohistochemical and immunofluorescence analyses were conducted to examine matrix metalloproteinase-2 (MMP-2), cyclooxygenase 2 (COX-2), cathepsin K, members of the receptor activator of the nuclear factor kappa-Β ligand (RANKL), receptor activator of nuclear factor kappa-Β (RANK), osteoprotegerin (OPG) pathway, macrophage migration inhibitory factor (MIF), superoxide dismutase-1 (SOD-1), glutathione peroxidase-1 (GPx-1), NFKB p 50 (Cytoplasm), NFKB p50 NLS (nuclear localization signal), PI3 kinase and AKT staining. Myeloperoxidase activity, malondialdehyde and glutathione levels, while interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) levels were evaluated by spectroscopic ultraviolet-visible analysis. A quantitative reverse transcription polymerase chain reaction was used to quantify the gene expression of the nuclear factor kappa B p50 subunit (NF-κB p50), phosphoinositide 3-kinase (PI3k), protein kinase B (AKT), and F4/80. Results Micro-computed tomography showed that the 1 mg/kg gliclazide treatment reduced linear bone loss compared to the ligature, 5 mg/kg gliclazide, and 10 mg/kg gliclazide treatments. All concentrations of gliclazide increased bone volume/tissue volume (BV/TV) compared to the ligature group. Treatment with 1 mg/kg gliclazide reduced myeloperoxidase activity, malondialdehyde, IL-1β, and TNF-α levels (p≤0.05), and resulted in weak staining for COX-2, cathepsin k, MMP-2, RANK, RANKL, SOD-1, GPx-1,MIF and PI3k. In addition, down-regulation of NF-κB p50, PI3k, AKT, and F4/80 were observed, and OPG staining was strong after the 1 mg/kg gliclazide treatment. Conclusions This treatment decreased neutrophil and macrophage migration, decreased the inflammatory response, and decreased bone loss in rats with ligature-induced periodontitis.

Evaluating clinical and laboratory effects of ozone in non-surgical periodontal treatment: a randomized controlled trial

Abstract Objective: This study aims to evaluate the clinical and biochemical (oxidative stress and pro-inflammatory mediators) effects of the gaseous ozone use accompanied by scaling and root planning (SRP) in periodontal treatment. Material and Methods: The study population consisted of 40 patients with chronic periodontitis (CP) randomly sorted into two groups of 20. The experimental group received SRP plus 3 watts gaseous ozone in two separate applications five days apart, whereas the control group received SRP plus placebo. Clinical periodontal parameters were assayed and saliva samples were taken before the initial and one month after the second treatment. Periodontal examination assessed plaque index (PI), gingival index (GI), probing depth, and clinical attachment level (CAL). Total antioxidant status (TAS), total oxidant status (TOS), nitric oxide (NO), 8-hydroxy-2'-deoxyguanosine (8-OHdG), myeloperoxidase (MPO), glutathione (GSH), malondialdehyde (MDA), and transforming growth factor-beta (TGF-β) levels were evaluated from saliva samples. Results: Changes following treatment in PI, GI, probing depth, and CAL scores were similar for both groups (p>0.05). Of note, TGF-β levels were observed to be higher in the treatment group than in controls (p<0.05). Changes in 8-OHdG, TAS, TOS, NO, MPO, GSH and MDA levels, however, were not significantly different between groups (p>0.05). Conclusion: The findings of this study indicate that SRP plus gaseous ozone versus SRP alone does not correlate to a significant improvement in periodontal recovery.

Effect of grape seed extract on bond strength of restorative material to bleached enamel

Objective: The aim of this study was to evaluate the effect of different concentrations of a natural antioxidant (grape seed extract) on the bond strength of the restorative material to the bleached enamel. Methods: Forty fragments of healthy bovine incisors were randomly divided into four groups (n = 10): Group I: no bleaching; Group II: Bleaching with 35% hydrogen peroxide (HP) and without post-treatment; Group III: Bleaching with 35% HP + 5% grape seed extract; and Group IV: Bleaching with 35% HP + 10% grape seed extract. The bond strength at the adhesive interface was evaluated using the shear test (MPa). The data were analyzed by the analysis of variance (ANOVA) and Tukey test ( =0.05%). The fracture types were also analyzed and classified into: adhesive, cohesive or mixed. Results: Only Group III (bleached + 5% grape seed extract) had a significant increase (p<0.001) in bond strength values when compared to Group II bleached, without post- reatment). All groups showed a predominance of the adhesive type of fracture. Conclusion: It could be concluded that tooth bleaching decreases the bond strength to bleached enamel and 5% grape seed extract applied after dental bleaching improves the bond strength between the restorative material and the bleached enamel.

Objetivo: Este trabalho teve por objetivo avaliar in vitro o efeito de um antioxidante natural (extrato de semente de uva) em diferentes concentrações, na resistência de união do material restaurador ao esmalte clareado. Métodos: Quarenta fragmentos de incisivos bovinos hígidos, foram divididos aleatoriamente em quatro grupos (n=10): Grupo I: sem clareamento; Grupo II: clareado com peróxido de hidrogênio 35% (PH) e sem pós-tratamento; GIII: clareado PH 35% + extrato de semente de uva 5%; e Grupo IV: clareado com PH 35% + extrato de semente de uva 10%. A resistência de união da interface esmalte/material restaurador foi avaliada por meio do teste de cisalhamento (MPa). Os dados foram analisados pela análise de variância (ANOVA) e testes de Tukey ( =0,05%). Os tipos de fratura também foram analisados e classificados em: adesiva, coesiva ou mista. Resultados: Apenas o Grupo III (clareado + extrato de semente de uva 5%) apresentou aumento estatisticamente significante (p<0,001). dos valores de resistência de união comparado ao Grupo II (clareado e sem pós-tratamento). Todos os grupos mostraram um predomínio do tipo de fratura adesiva. Conclusão: O clareamento dental diminui significativamente a força de adesão ao esmalte dental clareado, e o extrato de semente de uva 5% aplicado após o clareamento dental melhora a resistência de união entre o material restaurador e o esmalte clareado.

Comparative Study of the Efficacy of Newer Antioxitands Lycopene and Oxitard in the Treatment of Oral Submucous Fibrosis

Objective: To compare the efficacy of oxitard and lycopene in the management of Oral Submucous Fibrosis (OSMF). Material and Methods: 120 subjects with clinicpathologically diagnosed OSMF were included in the study and divided equally in 2 groups, Group A (oxitard) and Group B (lycopene). Group A was administered 2 oxitard capsules twice daily and Group B was given 8 mg lycopene in 2 divided doses of 4 mg for 3 months. Gingival index and plaque index were documented for all patients and compared. Evaluation for different clinical parameters was done at regular intervals and data was analyzed using the Student's paired t test and Chi-square test. P-value <0.001 was considered to be statistically significant. Results: Clinical improvements in mouth opening and tongue protrusion was significant in Group A (p<0.001). Subjective symptoms of pain associated with the lesion (p=0.0001), difficulty in swallowing (p=0.0004) and speech (p=0.0002) significantly improved in the Group A. However, there was no significant improvement in burning sensation (p>0.001) among the 2 groups. Although the mean gingival index and plaque index in group A was reduced but it was found to be not statistically significant. Conclusion: Oxitard capsules can bring about significant clinical improvements in the symptoms like mouth opening, tongue protrusion, difficulty in swallowing and speech and pain associated with the lesion when compared to lycopene, thereby improving the quality of life of the affected individuals.

A severidade da lesão de cárie induz maior atividade de sistemas antioxidantes e consequente redução do estresse oxidativo na saliva de crianças / Carious lesion severity induces higher activity of antioxidant systems and consequent reduction of oxidative stress in saliva of children

O objetivo deste estudo foi avaliar a relação entre os níveis de biomarcadores de estresse/ dano oxidativo na saliva de crianças e a severidade de cárie dentária classificada pelo Sistema Internacional de Classificação e Gerenciamento de Cárie (ICCMS™, termo em inglês International Caries Classification and Management System). Amostras de saliva não estimuladas foram coletadas de pacientes de 1-3 anos de idade, após 2 horas de jejum, no período da manhã, em uma creche do município de Birigui, SP, Brasil. As crianças foram divididas em 4 grupos (n=30/grupo), de acordo com a severidade de cárie, sendo livre de cárie (grupo A), lesão de cárie em estágio inicial (grupo B), lesão de cárie intermediaria (grupo C) e lesão de cárie em estágio avançado (grupo D). Foram avaliados os seguintes biomarcadores salivares de estresse oxidativo: dano oxidativo ou malonaldeído (MDA), mensurado pelo método de TBARS; capacidade antioxidante total (TAC), medida pelo ensaio do poder antioxidante férrico redutor; atividade antioxidante enzimática da superóxido dismutase (SOD) e atividade antioxidante não enzimática do ácido úrico (UA). Os dados foram analisados por ANOVA, seguido do teste de Student-Newman-Keuls, coeficientes de correlação de Pearson e Spearman, e regressão linear multivariada (p <0,05). Os resultados demonstraram que a quantidade de proteína total, TAC, atividade antioxidante enzimática e não-enzimática salivar aumentaram de acordo com a severidade das lesões de cárie, levando a redução do dano oxidativo salivar. Podemos concluir que quanto maior a severidade das lesões de cárie, maior atividade dos sistemas antioxidantes salivares, havendo, consequentemente, diminuição gradual do dano oxidativo salivar(AU)

The objective of this study was to evaluate the relationship between the levels of biomarkers of oxidative stress / oxidative damage in children's saliva and the severity of dental caries classified by the International Caries Classification and Management System (ICCMSTM). Unstimulated saliva samples were collected from patients 0-3 years old after 2 hours of fasting in the morning in a day care center in Birigui municipality. The children were divided into 4 groups (n = 30 / group), according to caries severity, being caries free (group A), early caries lesion (group B), intermediate caries lesion (group C) and advanced carious lesion (group D). The following salivary biomarkers of oxidative stress were evaluated: oxidative or malonaldehyde damage (MDA), measured by the TBARS method; total antioxidant capacity (TAC), as measured by the ferric reducing antioxidant power test; enzymatic antioxidant activity of superoxide dismutase (SOD) and non-enzymatic antioxidant activity of uric acid (UA). Data were analyzed by ANOVA, followed by Student-Newman-Keuls test, Pearson and Spearman correlation coefficients, and multivariate linear regression (p <0.05). The results showed that the concentration of total protein, TAC, enzymatic antioxidant and non-enzymatic salivary activity increased according to the severity of caries lesions, leading to reduction of salivary oxidative damage. We can conclude that the greater the severity of caries lesions, the greater the activity of the salivary antioxidant systems, and consequently the gradual decrease of salivary oxidative damage(AU)

Effects of grape seed extract on periodontal disease: an experimental study in rats

Abstract Natural compounds capable of modulating the host response have received considerable attention, and herbal products are suggested as adjunctive agents in periodontal disease treatment. Objective This study aimed to demonstrate the effect of grape seed extract (GSE) on periodontitis. Material and Methods Ligature induced periodontitis was created in 40 rats and they were assigned to four equal groups. One group was fed laboratory diet (group A) while three groups received GSE additionally. Silk ligatures were placed around the cervical area of the mandibular first molars for four weeks to induce periodontitis. The GSE groups were reallocated regarding GSE consumption as: for two weeks before ligation (group B; totally eight weeks), from ligation to two weeks after removal of the ligature (group C; totally six weeks), and for two weeks from ligature removal (group D; totally two weeks). Sections were assessed histologically and immunohistochemically. Inflammatory cell number (ICN), connective tissue attachment level (CAL), osteoclast density (OD), IL-10 and TGF-β stainings in gingival epithelium (GE), connective tissue (GC), and periodontal ligament (PL) were used as the study parameters. Results Lower ICN, higher CAL, and lower OD were observed in the GSE groups (p<0.05). IL-10 was more intensive in the GSE groups and in the GEs (p<0.05). Group B showed the highest IL-10 for PL (p<0.05). TGF-ß was higher in the GEs of all groups (p<0.017). Conclusions The results suggest anti-inflammatory activities of GSE, but further investigations are needed for clarification of these activities.

Efeitos da atividade física sobre a memória e estresse oxidativo plasmático e hipocampal de ratas na senescência / Effects of physical activity on memory, plasma and hippocampal oxidative stress of rats on senescence

Há evidências que a prática regular de atividade física potencializa a memória, diminui o estresse oxidativo plasmático e hipocampal e a ansiedade na senescência. Neste trabalho foram utilizadas 40 ratas (Rattus norvegicus albinus, Wistar), com 13 meses de idade ao início do experimento, divididas em quatro grupos: um grupo controle (GC) e três grupos tratamento (GT1, GT2 e GT3), sendo 10 animais em cada grupo. O grupo controle foi mantido apenas sob observação. Aos grupos tratamento foram aplicados exercícios físicos e de memória, sendo que ao GT1, apenas exercícios de memória; ao GT2 escalada em escada, e ao GT3 ambos os exercícios. Os animais que foram submetidos à escalada em escada três vezes por semana durante três meses consecutivos e aos testes de memória, apresentaram melhor desempenho nas memórias de curto e longo prazo e de habituação, bem como menor ansiedade em teste de campo aberto. A baixa concentração de malonaldeído (MDA), o equilíbrio da superóxido dismutase (SOD) e o aumento da capacidade antioxidante total (Ferric Reducing Antioxidant Power- FRAP, foram observados nas amostras plasmáticas e hipocampais de ratas submetidas aos tratamentos. Concluiu-se que a prática de exercício físico regular associado a exercícios de memória melhorou as capacidades mnemônicas, diminuiu o estresse oxidativo e a ansiedade de ratas na senescência(AU)

There is evidence that regular physical activity enhances memory, decreases plasma and hippocampal oxidative stress, and anxiety in senescence. In this work, 40 rats (Rattus norvegicus albinus, Wistar), 13 months old at the start of the experiment, were divided into four groups: one control group (CG) and three treatment groups (GT1, GT2 and GT3), 10 animals in each group. The control group was kept under observation only. In the treatment groups, physical and memory exercises were applied, and to GT1, only memory exercises; to GT2 climbing stairs, and to GT3 both exercises. Animals that underwent ladder climbing three times a week for three consecutive months and memory tests showed better performance in short and long term memory and habituation as well as lower anxiety in the open field test. The low concentration of malonaldehyde (MDA), the balance of superoxide dismutase (SOD) and the increase in total antioxidant capacity (Ferric Reducing Antioxidant Power - FRAP) were observed in the plasma and hippocampal samples of rats submitted to treatments. Regular exercise practice associated with memory exercises improved mnemonic abilities, decreased oxidative stress and anxiety of rats in senescence(AU)

Avaliação do efeito antioxidante do chá verde gel a 10% na resistência à tração de sistemas adesivos aplicados ao esmalte dental após clareamento e manutenção com dentifrício branqueador: estudo in vitro / Evaluation of the antioxidant effect of 10% green tea gel on the tensile strength of adhesive systems applied to dental enamel after bleaching and maintenance with bleaching dentifrice: in vitro study

O objetivo deste estudo in vitro foi avaliar a influência do tratamento antioxidante com chá verde gel (CV) a 10% na resistência adesiva à microtração dos sistemas adesivos frasco único, à base de etanol, Single Bond Universal (SBU), e mulltifrascos, à base de água, Adper Scotchbond Multiuso Plus (SBMU), quando aplicados ao esmalte dental clareado com peróxido de carbamida gel a 16% (Whiteness Perfect 16%- WP16%) e/ou através da escovação com dentifrício branqueador contendo peróxido de hidrogênio 1% (Colgate Luminous White Advanced- LW1%). Oitenta fragmentos dentais, com superfícies em esmalte planificadas e lisas, obtidos da face vestibular coronária de incisivos bovinos hígidos e recém extraídos, foram distribuídos aleatoriamente em 8 grupos experimentais (n=10) de acordo com os diferentes tratamentos: G1 e G5: Clareamento com WP16% + escovação com LW1%; G2 e G6- Clareamento com WP16% + escovação com LW1%+ aplicação CV; G3 e G7- Escovação com LW1%; G4 e G8- Escovação com LW1%+ aplicação CV. Nos grupos 1, 2, 3 e 4 foi aplicado o sistema adesivo SBU e nos grupos 5, 6, 7 e 8 o sistema SBMU, utilizados conforme instruções dos seus fabricantes. Em seguida, as superfícies dentais hibridizadas foram restauradas com o compósito NT Premium.Após o armazenamento em água destilada por 24 horas, os conjuntos fragmento dental/resina composta foram seccionados nos sentidos mésio/distal e vestíbulo/lingual para a obtenção de espécimes com aproximadamente 1,00 mm2 de área, e posteriormente submetidos ao teste de microtração realizado a uma velocidade de 1,0 mm/min. O teste estatístico de Dunn revelou haver diferenças significativas entre os grupos (p<0,05). Os valores em MPa foram: G2-57,99a; G4-57,18a; G3-53,62b; G8-49,69c; G6-48,92c; G1-42,44d; G7-37,50e; G5- 34,38e. O resultado do teste de Mann-Whitney, em MPa, mostrou haver diferenças significativas em função do sistema adesivo utilizado: SBU- 54,52a, SBMU-42,67b; do tipo de clareamento: LW1%- 52,17a, WP16%+LW1%-45,34b; e em função da aplicação ou não do antioxidante chá verde gel a 10%: PRESENTE- 54,26a, AUSENTE- 40,97b. Concluiu-se que o uso do Chá Verde Gel a 10% foi efetivo em aumentar a resistência à microtração dos adesivos aplicados ao esmalte clareado, sendo os maiores valores apresentados pelo SBU, adesivo à base de etanol. As duas técnicas clareadoras apresentaram os menores resultados de resistência adesiva para ambos os sistemas adesivos, porém, os resultados obtidos quando somente a escovação com LW1% foi realizada foram significativamente maiores do que os resultados observados quando esta foi associada ao WP16%. (AU)

The objective of this in vitro study was to evaluate the influence of the antioxidant treatment with 10% green tea gel (CV) on the microtensile bond strength of a single bottle adhesive system, an ethanol base Single Bond Universal (SBU), and a multiple bottles adhesive system, a water base Adper Scotchbond Multipurpose Plus (SBMU), when applied to dental enamel whitened with 16% carbamide peroxide gel (Whiteness Perfect 16%- WP16%) and/or by brushing with whitening dentifrice containing 1% hydrogen peroxide (Colgate Luminous White Advanced- LW1%). Eighty dental fragments with smooth and planned enamel surfaces obtained from the coronary vestibular surface of healthy freshly extracted bovine incisors were randomly distributed in 8 experimental groups (n= 10) according to the different treatments: G1 and G5: Whitening with WP16% + brushing with LW1%; G2 and G6- Whitening with WP16% + brushing with LW1% + CV application; G3 and G7- Brushing with LW1%; G4 and G8- Brushing with LW1% + CV application. In groups 1, 2, 3 and 4 the SBU adhesive system was applied and in groups 5, 6, 7 and 8 the SBMU system was used as instructed by its manufacturers and then the hybridized dental surfaces were restored with NT Premium composite resin.After storage in distilled water for 24 hours, the sets of dental fragments/composite resin were serially sectioned in a mesial/distal and buccal/lingual directions to obtain specimens with approximately 1.00 mm2 of area, subsequently individually submitted to the tensile test performed at a 1.0 mm/min crosshead speed. The Dunn test revealed significant differences between groups (p<0.05). The values in MPa were: G2-57.99a; G4-57.18a; G3-53.62b; G8-49.69c; G6-48.92c; G1-42.44d; G7-37.50e; G5- 34.38e. The results of the Mann-Whitney test, in MPa, showed significant differences as a function of the adhesive system used: SBU-54,52a, SBMU-42,67b; The whitening type: LW1% - 52.17a, WP16% + LW1%- 45.34b; And depending on the application or not of the antioxidant 10% green tea gel: PRESENT- 54,26a, ABSENT- 40,97b. It was concluded that the 10% green tea gel was effective in recovering the microtensile bond strength of the adhesive systems applied to the enamel bleached by the two methods used, with the highest values observed for the groups in which the ethanol base Single Bond Universal system was used. The results obtained when only toothbrushing with bleaching dentifrice was performed were significantly higher than the results observed when it was associated with the 16% carbamide peroxide gel. (AU)

In vitro evaluation of the effect of antioxidants on the bond strength of bleached teeth / Avaliação in vitro do efeito de antioxidantes sobre a resistência de união de dentes clareados

Objective: To evaluate the in vitro effect of antioxidants on the bond strength between composite resin and enamel subjected to bleaching agents. Methods: Nineteen sound human molars had their roots sectioned, while their surfaces were flattened and filled with composite resin to produce the specimens, which were then divided into seven groups: G1 ­ unbleached and without antioxidant (control); G2 ­ 36% carbamide peroxide; G3 ­ 36% carbamide peroxide and 10% ascorbic acid solution; G4 ­ 36% carbamide peroxide and 10% ascorbic acid gel; G5 ­ 16% carbamide peroxide; G6 ­ 16% carbamide peroxide and 10% ascorbic acid solution; and G7 ­ 16% carbamide peroxide and 10% ascorbic acid gel. The results of microtensile strength were submitted to an analysis of variance (ANOVA) and Tukey's test, with a significance level of 5%. Results: The bond strength between composite resin and enamel was not affected after the use of bleaching agents. In addition, ascorbic acid did not appear to neutralize the oxidative effects of these agents, given that group 3 showed the lowest mean of bond strength (13.85 MPa). In other groups, the mean of bond strength ranged from 24.06 MPa to 32.02 MPa, with no significant differences when compared to the control. Conclusion: The presence of ascorbic acid immediately after bleaching did not increase the bond strength between the resin and the enamel surface.(AU)

Objetivo: Avaliar in vitro o efeito de antioxidantes sobre a resistência de união entre resina composta e o esmalte sujeito a agentes clareadores. Métodos: Dezenove molares humanos hígidos tiveram suas raízes seccionadas e suas superfícies planificadas e restauradas para obtenção dos corposde-prova, os quais foram divididos em sete grupos: G1 - não clareado e sem agente antioxidante (controle); G2 - Peróxido de carbamida a 36%; G3 - Peróxido de carbamida a 36% e Ácido ascórbico 10% solução; G4 - Peróxido de carbamida a 36% e Ácido ascórbico 10% gel; G5 - Peróxido de carbamida a 16%; G6 - Peróxido de carbamida a 16% e Ácido ascórbico 10% solução; G7 - Peróxido de carbamida a 16% e Ácido ascórbico 10% gel. Os resultados da resistência a microtração foram submetidos à análise de variância (ANOVA) e ao teste de Tukey em nível de significância 5%. Resultados: A resistência adesiva entre resina e o esmalte não foi afetada após a utilização dos agentes clareadores, além disto, o ácido ascórbico não se apresentou capaz de neutralizar os efeitos oxidantes destes agentes, tendo em vista que o grupo 3 mostrou menor média quanto a resistência de união (13,85 Mpa). Nos demais grupos, as médias variaram de 24,06 Mpa a 32,02 Mpa, não havendo diferença significante entre essas médias e o controle. Conclusão: A presença do ácido ascórbico logo após o clareamento dentário não aumento a resistência de união entre a resina e a superfície do esmalte.(AU)

Evaluation of antioxidant efficacy of Purslane extract in Patients with Recurrent Aphthous Stomatitis: a randomized, placebo-controlled, triple-blinded, clinical trial

Background: This herbal medicine is considered a rich source of antioxidants with anti-inflammatory effects. The purpose of this study was to evaluate the effectiveness of purslane in treatment of recurrent aphthous stomatitis (RAS) and also it ̓s effect on antioxidant level. Materials and methods: 50 patients were selected for this randomized triple-blind placebo-controlled trial. All subjects were randomly divided in to two groups, one group received purslane (n=25) and another group, placebo (n=25) for 3 month. Superoxide dismutase (SOD), glutathione peroxidase (GSHPx) and total antioxidant status (TAS) was measured in plasma at baseline and after 3 month of treatment. Also pain intensity based on the visual analogue scale (VAS), the mean interval between lesion, number of lesions and the mean duration of complete healing at baseline and in month 1, 2 and 3 were recorded. Statistical analysis was performed by using Mann-Whitney and T-test. Results: A significant decrease in pain intensity in VAS scores was seen after treatment in intervention group (p<0.001). The mean duration of complete healing showed significant differences (P<0.001) between the two groups. The mean interval between lesions also showed significant differences (P<0.001) among the intervention group (33.12 days) compared with the placebo group (17.88 days). No significant differences were found regarding the number of lesions, level of erythrocyte GSHPx, TAS and SOD. No serious side-effects occurred in either of groups. Conclusions: According to this study, purslane is clinically effective in treatment of RAS (number of lesions, pain intensity and duration of healing) although it is unable to change the level of antioxidants. (AU)