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Introduction: Right ventricular remodeling with subsequent functional impairment can occur in some clinical conditions in adults and children. The triggering factors, molecular mechanisms, and, especially, the evolution over time are still not well known. Left ventricular (LV) changes associated with right ventricular (RV) remodeling are also poorly understood. Objectives: The study aimed to evaluate RV morphological, functional, and gene expression parameters in rats submitted to pulmonary artery banding compared to control rats, with the temporal evolution of these parameters, and to analyze the influence of RV remodeling by pulmonary artery banding in rats and their controls over time on LV geometry, histology, gene expression, and functional performance. Methods: Healthy 6-week-old male Wistar-EPM rats weighing 170-200 g were included. One day after the echocardiogram, depending on the animals undergoing the pulmonary artery banding (PAB) procedure or not (control group), they were then randomly divided into subgroups according to the follow-up time: 72 h, or 2, 4, 6, or 8 weeks. In each subgroup, the following were conducted: a new echocardiogram, a hemodynamic study, the collection of material for morphological analysis (hypertrophy and fibrosis), and molecular biology (gene expression). The results were presented as the mean ± standard deviation of the mean. A two-way ANOVA and Tukey post-test compared the variables of the subgroups and evolution follow-up times. The adopted significance level was 5%. Results: There was no significant difference among the subgroups in the percentage of water in both the lungs and the liver (the percentage of water in the lungs ranged from 76% to 78% and that of the liver ranged from 67% to 71%). The weight of the right chambers was significantly higher in PAB animals in all subgroups (RV PAB weighed from 0.34 to 0.48 g, and control subjects, from 0.17 to 0.20 g; right atrium (RA) with PAB from 0.09 to 0.14 g; and control subjects from 0.02 to 0.03 g). In the RV of PAB animals, there was a significant increase in myocyte nuclear volume (97 µm3-183.6 µm3) compared to control subjects (34.2 µm3-57.2 µm3), which was more intense in subgroups with shorter PAB follow-up time, and the fibrosis percentage (5.9%-10.4% vs. 0.96%-1.18%) was higher as the PAB follow-up time was longer. In the echocardiography result, there was a significant increase in myocardial thickness in all PAB groups (0.09-0.11 cm compared to control subjects-0.04-0.05 cm), but there was no variation in RV diastolic diameter. From 2 to 8 weeks of PAB, the S-wave (S') (0.031 cm/s and 0.040 cm/s), and fractional area change (FAC) (51%-56%), RV systolic function parameters were significantly lower than those of the respective control subjects (0.040 cm/s to 0.050 cm/s and 61%-67%). Furthermore, higher expression of genes related to hypertrophy and extracellular matrix in the initial subgroups and apoptosis genes in the longer follow-up PAB subgroups were observed in RV. On the other hand, LV weight was not different between animals with and without PAB. The nuclear volume of the PAB animals was greater than that of the control subjects (74 µm3-136 µm3; 40.8 µm3-46.9 µm3), and the percentage of fibrosis was significantly higher in the 4- and 8-week PAB groups (1.2% and 2.2%) compared to the control subjects (0.4% and 0.7%). Echocardiography showed that the diastolic diameter and LV myocardial thickness were not different between PAB animals and control subjects. Measurements of isovolumetric relaxation time and E-wave deceleration time at the echocardiography were different between PAB animals and control subjects in all subgroups, but there were no changes in diastolic function in the hemodynamic study. There was also increased expression of genes related to various functions, particularly hypertrophy. Conclusion: 1) Rats submitted to pulmonary artery banding presented RV remodeling compatible with hypertrophy. Such alterations were mediated by increased gene expression and functional alterations, which coincide with the onset of fibrosis. 2) Structural changes of the RV, such as weight, myocardial thickness, myocyte nuclear volume, and degree of fibrosis, were modified according to the time of exposure to pulmonary artery banding and related to variations in gene expression, highlighting the change from an alpha to a beta pattern from early to late follow-up times. 3) The study suggests that the left ventricle developed histological alterations accompanied by gene expression modifications simultaneously with the alterations found in the right ventricle.
RESUMO
Objective: The present study aims to verify the effectiveness of in-office dental bleaching using 35% hydrogen peroxide in patients with or without a habit of consuming coffee at least three times per day at different time intervals (pre-bleaching or baseline;48 hours post-bleaching or start; and 90 days post-bleaching or recall). Methods and Material - Forty patients with superior and inferior vital teeth from canine to canine participated in this study. The optical measurements with SpectroShade Microspectrophotometer (MHT, Verona, Italy) determined the pre-bleaching status (baselinemeasurement), the status at 48 hours post-bleaching (start measurement), and thestatus at 90 days post-bleaching (recall measurement). The Delta E (ΔE) value was determined, and the difference between the pre- and post-bleaching luminosity was used as an indicator of the degree of chromogenic alteration. The patients were divided into four groups according to the presence or absence of a coffee ingestion habit and according to different post-bleaching time intervals. These data were analyzed by ANOVA and in case of significant differences the mean values were compared usingthe Tukey test (p < 0.05). Results and Conclusions - In conclusion, it was possible to confirm that professional dental bleaching is an effective technique that can be usedboth in patients who drink and do not drink coffee. However, the maintainability of this treatment was significantly reduced in the group of patients who habitually drink coffee within a period of only 90 days
Objetivos: O presente estudo visa verificar a efetividade do clareamento dental profissional utilizando o peróxido de hidrogênio a 35% em pacientes com e sem o hábito de ingestão de café por pelo menos três vezes ao dia em diferentes intervalosde tempo (pré-clareamento ou baseline; 48 horas pós-clareamento ou start; e 90 diaspós-clareamento ou recall). Material e Métodos - Quarenta pacientes com dentes naturais inferiores e superiores participaram deste estudo. As tomadas de cor com o espectrofotômetro SpectroShade (MHT, Verona, Itália) determinaram a condição pré clareamento(medição baseline), a condição em 48 horas pós-clareamento (medição start),e a condição após 90 dias (medição recall). O valor de Delta E (ΔE) foi determinado, e a diferença entre a luminosidade na condição pré e pós-clareamentos foram utilizadas como o indicador do grau de alteração cromatogênica. Os pacientes foram divididos em quatro grupos de acordo com a presença ou ausência de hábitos de ingestão de café e dos diferentes períodos pós-clareamento. Os dados foram analisados via ANOVA e, quando necessário, os valores médios foram comparados utilizando o teste de Tukeya 5% de significância (p < 0.05). Resultados e Conclusões - Como conclusão foi possível confirmar que clareamento dental profissional é uma técnica efetiva e que pode ser utilizada tanto em pacientes que ingerem como nos que não ingerem café. Contudo, a durabilidade deste tratamento clareador é significativamente reduzida no grupo de pacientes que habitualmente bebem café dentro de um período relativamente curto, ou seja, de apenas 90 dias
