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The aim of this in vitro study was to evaluate the protective effect of short-pulsed CO2 9.3 µm laser irradiation against erosion in human enamel without and combined with TiF4 and AmF/NaF/SnCl2 applications, respectively, as well as compared to the protective effect of these fluoride treatments alone. After polishing, ninety enamel samples (3 × 3mm) were used for 9 different treatment groups: 4% TiF4 gel (pH 1.5, 24,533 ppm F-); AmF/NaF/SnCl2 rinse (pH 4.5; 500 ppm F-, 800 ppm Sn2); CO2 laser (average power 0.58 W); CO2 laser (0.58 W) + TiF4; CO2 laser (0.58 W) + AmF/NaF/SnCl2; CO2 laser (0.69 W); CO2 laser (0.69 W) + TiF4; CO2 laser (0.69 W) + AmF/NaF/SnCl2; negative control (deionized water). TiF4 gel was brushed on only once before the first erosive cycling, while samples treated with AmF/NaF/SnCl2 were daily immersed in 5 ml of the solution before cycling. Laser treatment occurred with a CO2 laser (wavelength 9.3 µm, pulse repetition rate 100 Hz, pulse duration 14.6 µs/18 µs, average power 0.58 W/0.69 W, fluence 1.9 J/cm2/2.2 J/cm2, beam diameter 0.63 mm, irradiation time 10 s, air cooling). TiF4 was applied only once, while AmF/NaF/SnCl2 was applied once daily before the erosive challenge. Surface loss (in µm) was measured with optical profilometry immediately after treatment, and after 5 and 10 days of erosive cycling (0.5% citric acid, pH 2.3, 6 × 2 min/day). Additionally, scanning electron microscopy investigations were performed. All application measures resulted in loss of surface height immediately after treatment. After 5 days, significantly reduced surface loss was observed after applying laser irradiation (both power settings) followed by applications of TiF4 or AmF/NaF/SnCl2 solution (p < 0.05; 2-way ANOVA and Tukey test) compared to fluoride application alone. After 10 days, compared to after 5 days, a reduced tissue loss was observed in all groups treated with AmF/NaF/SnCl2 solution. This tissue gain occurred with the AmF/NaF/SnCl2 application alone and was significantly higher when the application was combined with the laser use (p < 0.05). Short-pulsed CO2 9.3 µm laser irradiation followed by additional application of AmF/NaF/SnCl2 solution significantly reduces the progression of dental enamel erosion in vitro.

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Although several studies have demonstrated the efficacy of AmF/NaF/SnCl2 solution in inhibiting dental erosion progression, measures for further improvement in its effectiveness are paramount. Thus, this in situ study evaluated whether the protective effect promoted by the AmF/NaF/SnCl2 solution would be enhanced by increasing its frequency of use. The study was conducted with 12 volunteers, a 4-phase (5 days each) randomized, crossover model. Extraoral erosive challenges (0.5% citric acid, pH 2.6, 6 × 2 min/day) and rinsing protocol (1 or 2 × 2 min/day) were performed. Before the in situ phase, human enamel samples were subjected to an in vitro surface softening (1% citric acid, pH 4.0, for 3 min). Four treatment protocols were tested using samples in replicas (n = 12): group G1 - deionized water (negative control); G2 - NaF solution (positive control, 500 ppm F-, pH 4.5); G3 - AmF/NaF/SnCl2 solution (500 ppm F-, 800 ppm Sn2+, pH 4.5) once a day; G4 - AmF/NaF/SnCl2 solution twice a day. Tissue loss and morphological changes were determined by optical profilometry (n = 12) and scanning electron microscopy (n = 3) analysis, respectively. Data were statistically analyzed by ANOVA with subsequent pairwise comparison of treatments. Tissue loss means (±SD in µm) for each treatment protocol and statistical differences were found as follows: G1 4.55 ± 2.75, G2 4.59 ± 2.13, G3 2.64 ± 1.55, and G4 1.34 ± 1.16. Although there was no difference between the 2 AmF/NaF/SnCl2 solution application regimens (once or twice a day), application of the product twice a day was the only treatment that was able to control erosion progression, differing from the control groups.

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UNLABELLED: This cross-sectional study involves randomly selected men aged 50 to 99 years and postmenopausal women. Either central fat mass or peripheral fat mass were associated to osteoporosis or osteopenia independently from fat-free body mass and other confounding factors. INTRODUCTION: Obesity and osteoporosis are public health problems that probably share common pathophysiological mechanisms. The question if body fat mass, central or peripheral, is protective or harmful for osteoporosis or osteopenia is not completely resolved. This study aims to investigate the association between osteoporosis or osteopenia, and fat body mass (central and peripheral) independently from fat-free body mass, in men aged 50 to 99 years old and postmenopausal women randomly selected in the community. METHODS: This is a cross-sectional investigation with a random sample of registered population in Niterói Family Doctor Program (FDP), State of Rio de Janeiro, Brazil. Bone mineral density (BMD) and fat-free mass were assessed by dual X-ray absorptiometry (DXA). RESULTS: There was statistically significant bivariate association between bone loss with gender, age, skin color, alcohol consumption at risk dose, use of thiazide, fat-free body mass, and fat body mass (central and peripheral). In the multiple analysis of fat-free body mass, central and peripheral fat body mass showed an independent and protective effect on the presence of osteoporosis or osteopenia (p value <0.001). CONCLUSION: Since both obesity and osteoporosis are public health problems worldwide, strategies aimed at preventing both conditions should be encouraged during aging.

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Since all analgesics currently available for use in dogs have been associated with some adverse effects, the search for an effective analgesic that does not cause harm is important. This study investigated the postoperative analgesic effects of ozone administered either intrarectally or into acupoints in bitches undergoing ovariohysterectomy (OH). Twenty-four healthy adult bitches were randomly assigned to one of the three treatments 10 min after sedation, as follows: 0.2mg/kg of intramuscular (IM) meloxicam (M); rectal insufflation of 10 mL of 30 µg/mL ozone (OI), or acupoint injection of 0.5 mL ozone (30 µg/mL; OA). Following sedation with acetylpromazine, anaesthesia was induced with propofol and fentanyl and maintained with isoflurane/O2. Pain was assessed using the modified Glasgow pain scale (MGPS) and the visual analogue scale (VAS) on the day before surgery, before anaesthesia, and at 1, 2, 4, 6, 8, 12 and 24h after surgery. Rescue analgesia was performed using 0.5mg/kg of morphine IM if MGPS was >3.33 points. No statistically significant differences in pain scales were found among the three analgesic protocols or the time points in each group (P>0.05). Two dogs treated with OA required rescue analgesia. Meloxicam, rectal insufflation of ozone and ozone injected into acupoints provided satisfactory analgesia for 24h in bitches undergoing elective OH. Ozone had no measurable adverse effects and is an alternative option to promote pain relief.

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Background. To compare Child Behavior Checklist (CBCL) findings for a large Brazilian general population sample with those for US children considering: (a) mean problem item ratings; (b) fit of the US-derived CBCL 8-syndrome model; (c) scale internal consistency measured by Cronbach's alphas; (d) effects of society, age, gender on CBCL problem scores; and (e) ability to discriminate referred from non-referred children. Methods. Parents of 1228 non-referred 6-to-11-year-olds from three different regions of Brazil and 247 referred 6-to-11-year-olds from one clinic rated their children's behavioural and emotional problems using the CBCL/6-18. Results. Results for mean item ratings and scale internal consistencies were very similar to those found in the US and in Uruguay. Confirmatory factor analysis indicated that Brazilian data showed the best fit to the US 8-syndrome model of all countries studied to date. Gender patterns were comparable to those reported in other societies, but mean problem scores for non-referred Brazilian children were higher than those for US children. Therefore, the CBCL discriminated less well between non-referred and referred children in Brazil than in the US. Conclusions. Overall, our findings replicated those reported in international comparisons of CBCL scores for 31 societies, thereby providing support for the multicultural robustness of the CBCL in Brazil.

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Biocompatibilidade é a capacidade de um material exercer funções específicas quando aplicado em contato com tecidos vivos de determinado hospedeiro, sem, contudo, causar danos ou prejuízo ao mesmo. Este trabalho objetivou determinar a biocompatibilidade in vivo e in vitro do extrato hidroalcoólico do Cissus sicyoides L - Vitaceae. Foram utilizados 30 ratos (Rattus novergicus albinus wistar), com idade entre 45 e 90 dias e pesando entre 170 e 260 g. Os animais foram divididos em 3 grupos (A1, A2 e A3) de 6 animais cada para o teste in vivo, os quais foram sacrificados com 2, 4 e 6 dias, respectivamente. Para o teste in vitro, foram utilizados 12 animais para obtenção do índice de aderência e da capacidade fagocítica dos macrófagos de ratos do grupo controle e do grupo experimental. Nos resultados encontrados no teste in vivo, conclui-se que o extrato apresentou-se biocompatível, visto que não provocou alterações significativas no tecido. Já no teste in vitro, o mesmo não se apresentou biocompatível, pois o extrato puro apresentou índice de aderência baixo (7,1) e taxa de fagocitose elevada (35,7), indicando diferença significante quando comparado ao controle. Porém, quando diluído, o extrato se mostrou inócuo, devido ao aumento dos valores do índice de aderência nas concentrações de 1/10 (61,4) e 1/100 (74,3) nos ensaios, as quais não apresentaram diferença significante quando comparadas ao controle. Após a análise dos dados, concluiu-se que a solução diluída do extrato hidroalcoólico do Cissus sicyoides L. não causa danos ou prejuízos. Entretanto, como nem todos os efeitos farmacológicos foram testados no presente trabalho, não se pode inferir automaticamente que ele é biocompatível em todos os casos.

Biocompatibility is the ability of a material to perform specifictasks when applied to living tissues without causing damage or injuries to it. Thus, this study aimed at determining the in vivo and in vitro biocompatibility of Cissus sicyoides L. - Vitaceae hydroalcoholic extracts. A total of 30 rats (Rattus norvegicus Albinus Wistar), with ages ranging from 45 to 90 days and weighing between 170 and 260g were used. The animals were divided into 3 groups (A1, A2 and A3) with 6 animals each, for the in vivo test, which were sacrificed after 2, 4 and 6 days, respectively. For in vitro test, 12 animals were used to obtain the index of adherence and phagocytic ability of macrophages of rats from the control and the experimental groups. In results found for the in vivo test, it was concluded that the extract was biocompatible, whereas no significant changes were observed in the tissue. As to the in vitro test, the extract was not biocompatible, since the pure extract showed a low rate of adherence (7.1) and a high rate of phagocytosis (35.7), indicating a significant difference when compared to the control group. However, when diluted, the extract was shown to be harmless, due to an increase in the values of the adherence index at the following concentrations : 1/10 (61.4) and 1/100 (74.3) in the tests, which showed no significant differences when compared to the control group. After analyzing the data, it was concluded that since the infusion of the plant is a kind of dilution, its use does not cause any harm to the body. A new study is necessary at the moment to possibily demonstrate its effects on the long term.

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Quantitative computed tomography was used to determine the radiodensity of bony plates. The CT scans provided information regarding radiodensity of bony plates and allowed to verify the uniformity of bone mineral density in their scope. The proposed methodology should be considered as another tool for determining the resistance of these biomaterials.(AU)

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Quantitative computed tomography was used to determine the radiodensity of bony plates. The CT scans provided information regarding radiodensity of bony plates and allowed to verify the uniformity of bone mineral density in their scope. The proposed methodology should be considered as another tool for determining the resistance of these biomaterials.

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Avaliaram-se os efeitos analgésicos da eletroacupuntura, aquapuntura e farmacopuntura com morfina nos acupontos VB41 e TA5 de 24 cadelas hígidas submetidas à ovário-histerectomia. Os animais foram distribuídos em quatro grupos (G) de igual número - GDest, GMorf, GElet e GC - e anestesiados com acepromazina, propofol e isofluorano. Após a estabilização do plano anestésico, os animais do GDest receberam 0,5mL de água destilada em cada acuponto; os do GMorf receberam 0,1mg/kg de morfina distribuído nos quatro acupontos; os do GElet foram submetidos à eletroacupuntura; e os do GC, acupuntura em pontos sham. Os animais do GC receberam, após o término do procedimento cirúrgico e antes do início da avaliação pelas escalas de dor, 2,0mg/kg de tramadol. Foram avaliadas: frequências cardíaca e respiratória, temperatura retal e glicemia. A dor foi avaliada por duas escalas, uma de analogia numérica e outra contagem variável, por três observadores. A avaliação iniciou-se imediatamente após a extubação e foi realizada a cada 15 minutos, durante duas horas. Não houve diferença entre os tratamentos em todas as variáveis. Pode-se concluir que eletroacupuntura, aquapuntura e farmacopuntura com morfina resultaram em analgesia similar ao tramadol no pós-operatório imediato de cadelas submetidas à ovário-histerectomia eletiva.(AU)

In order to evaluate the analgesic effects of electro-acupuncture, aquapuncture and morphine pharmacopuncture on VB41and TA5 acupoints, 24 healthy bitches were anesthetized with acepromazine, propofol and isoflurane and underwent ovariohysterectomy. The animals were equally divided into four groups: GDest, GMorf, GElet and CG. After anesthetic stabilization, GDest animals received pure water (0.5ml per acupoint); GMorf received morphine (0.1mg/kg); electroacupuncture was performed in GElet animals, and CG animals were submitted to acupuncture on Sham points. The CG animals received 2.0mg/kg of tramadol after the end of surgery and before the postoperative evaluation through pain scales. Data recorded were: heart and respiratory rate, rectal temperature and blood glucose. Pain was assessed using two different scales, one using numerical analogy and another using variable counting, both performed by three different professionals. Evaluation started immediately after the animal was extubated and was performed every 15 minutes, for 2 hours. There was no statistical difference between groups in all variables studied. It is concluded that electro-acupuncture, aquapuncture and morphine pharmacopuncture produce analgesia similar to tramadol in the postoperative period of bitches undergoing elective ovariohysterectomy.(AU)

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Avaliaram-se os efeitos analgésicos da eletroacupuntura, aquapuntura e farmacopuntura com morfina nos acupontos VB41 e TA5 de 24 cadelas hígidas submetidas à ovário-histerectomia. Os animais foram distribuídos em quatro grupos (G) de igual número - GDest, GMorf, GElet e GC - e anestesiados com acepromazina, propofol e isofluorano. Após a estabilização do plano anestésico, os animais do GDest receberam 0,5mL de água destilada em cada acuponto; os do GMorf receberam 0,1mg/kg de morfina distribuído nos quatro acupontos; os do GElet foram submetidos à eletroacupuntura; e os do GC, acupuntura em pontos sham. Os animais do GC receberam, após o término do procedimento cirúrgico e antes do início da avaliação pelas escalas de dor, 2,0mg/kg de tramadol. Foram avaliadas: frequências cardíaca e respiratória, temperatura retal e glicemia. A dor foi avaliada por duas escalas, uma de analogia numérica e outra contagem variável, por três observadores. A avaliação iniciou-se imediatamente após a extubação e foi realizada a cada 15 minutos, durante duas horas. Não houve diferença entre os tratamentos em todas as variáveis. Pode-se concluir que eletroacupuntura, aquapuntura e farmacopuntura com morfina resultaram em analgesia similar ao tramadol no pós-operatório imediato de cadelas submetidas à ovário-histerectomia eletiva.

In order to evaluate the analgesic effects of electro-acupuncture, aquapuncture and morphine pharmacopuncture on VB41and TA5 acupoints, 24 healthy bitches were anesthetized with acepromazine, propofol and isoflurane and underwent ovariohysterectomy. The animals were equally divided into four groups: GDest, GMorf, GElet and CG. After anesthetic stabilization, GDest animals received pure water (0.5ml per acupoint); GMorf received morphine (0.1mg/kg); electroacupuncture was performed in GElet animals, and CG animals were submitted to acupuncture on Sham points. The CG animals received 2.0mg/kg of tramadol after the end of surgery and before the postoperative evaluation through pain scales. Data recorded were: heart and respiratory rate, rectal temperature and blood glucose. Pain was assessed using two different scales, one using numerical analogy and another using variable counting, both performed by three different professionals. Evaluation started immediately after the animal was extubated and was performed every 15 minutes, for 2 hours. There was no statistical difference between groups in all variables studied. It is concluded that electro-acupuncture, aquapuncture and morphine pharmacopuncture produce analgesia similar to tramadol in the postoperative period of bitches undergoing elective ovariohysterectomy.