Effects of aging on the secretory apparatus in the right atrial cardiomyocytes of rats.

The cardiac atria secrets polypeptide hormones usually called natriuretic peptides (NPs). These substances play a relevant role in the blood pressure regulation. The objective of the study was to estimate the effects of aging on the secretory apparatus of NPs in cardiomyocytes of the right atrium. Twenty male Wistar rats were studied: 10 young animals aged 3 months old (237 ±â€¯27 g; mean ±â€¯SD) and 10 old animals aged 20 months old (450 ±â€¯68 g; mean ±â€¯SD). The systolic blood pressure was verified instants before the moment of the euthanasia. Electron micrographs were prepared to quantify the area and density of the NP granules and the relative volumes of the endoplasmic reticulum, Golgi complex, and mitochondria. In addition, the number of pores per 10 µm of karyotheca was another variable evaluated. The significance of the results between the two groups evaluated was analyzed by the Student's t test (p < 0.05). The cardiomyocytes obtained from animals of the old group showed decreased in sectional area and density of secretory granules of NP and lower relative volume of endoplasmic reticulum, Golgi complex, and mitochondria compared with the young rats. Moreover, the quantitative density of nuclear pores was significantly lower compared with the youngers. CONCLUSION: Aging causes hypotrophy of the cardiomyocytes of right atrium, similar to what occurs in ventricular cardiomyocytes.

Anatomical Variation in the Mandibular Foramen in Non-Atrophic and Atrophic Mandibles.

OBJECTIVES: Previous studies of variation in mandibular foramen characteristics with age have involved comparison in different populations, but few data, between non-atrophic and atrophic mandibles are available. The aim of this original article was to compare the position, shape and area of the mandibular foramen between non-atrophic and atrophic mandibles. MATERIAL AND METHODS: Morphometric methods were used to study the mandibular foramen variation. Fifty adult dry mandibles from the laboratory of anatomy were selected. Mandibles were considered non-atrophic if the distance between the base and alveolar ridge was homogeneous and greater than 25 mm in the anterior region and 20 mm in the posterior region. Conversely, mandibles were considered atrophic if that distances were lower than those described to a minimum of 11 mm in all areas. All measurements were performed with a digital caliper. For statistical analysis, the admitted level of significance was 5%. RESULTS: When non-atrophic mandibles were compared to atrophic ones, the mandibular foramen shifted significantly to an anterior position (mean difference [MD]: 4.81 mm; P < 0.0001) and to an inferior position (MD: 3.04 mm; P < 0.0001) and changed from an elliptical shape to round one, with a significant decrease in its area (MD: 3.66 mm2; P < 0.05). CONCLUSIONS: The results indicate that there are significant differences in the position, shape and area of the mandibular foramen between non-atrophic and atrophic mandibles. These data should be considered in anaesthetic techniques and surgical procedures to prevent vascular and nervous lesions.

The Effects of Photobiomodulation Delivered by Light-Emitting Diode on Stem Cells from Human Exfoliated Deciduous Teeth: A Study on the Relevance to Pluripotent Stem Cell Viability and Proliferation.

OBJECTIVE: Photobiomodulation (PBM) can modulate the proliferation of some types of stem cells. However, few reports have addressed the effects of PBM delivered by light-emitting diode (LED) on stem cells obtained from the pulp tissue of deciduous teeth. The aim of the present study was to investigate the effect of PBM delivered by red LED (630 nm, 75 mW, 37 mW/cm2) with different radiant exposures on the cell cycle, mitochondrial membrane potential, and senescence of stem cells from human exfoliated deciduous teeth (SHED). MATERIALS AND METHODS: Cultures were irradiated with LED (2, 4, 8, 16, and 32 J/cm2). After 24 h, the cell cycle and mitochondrial membrane potential of the cultures were evaluated using flow cytometry. Nonirradiated cultures served as control. RESULTS: Cultures irradiated with 16 J/cm2 had higher percentages of cells in the synthesis phase than control cultures (p < 0.05), and no significant differences were found regarding the percentage of cells with viable mitochondria between irradiated and control cultures. No significant difference in cell senescence was found between control cultures and cultures irradiated with 2 or 16 J/cm2. CONCLUSIONS: LED irradiation at 630 nm (37 mW/cm2, 75 mW) with radiant exposure of 16 J/cm2 was capable of inducing a proliferative response in stem cells from the pulp tissue of deciduous teeth without affecting mitochondrial function or inducing senescence.

Pilot study on laser propagation in maxillary and mandibular bone: Grey level image analysis for optical measurements.

BACKGROUND: Bone tissue anatomy, density and porosity vary among subjects in different phases of life and even within areas of a single specimen. The optical characteristics of changes in bone tissue are analyzed based on these properties. Photobiomodulation has been used to improve bone healing after surgery or fractures. Thus, knowledge on light propagation is of considerable importance to the obtainment of successful clinical outcomes. OBJECTIVE: This study determines light penetration and distribution in human maxillary and mandibular bones in three different regions (anterior, middle, and posterior). METHODS: A HeNe laser (633nm) irradiated maxillary and mandibular bones in the cervical-apical direction. The light propagation and scattering pattern were acquired and the grey level of the images was analyzed. Three-dimensional plots of the intensity profile and attenuation profiles were created. RESULTS: Differences in optical properties were found between the mandibular and maxillary bones. The maxilla attenuated more light than the mandible at all sites, leading to a shallower penetration depth. CONCLUSION: Our results provide initial information on the behavior of the propagation of red laser on alveolar bone using an optical method.

MORPHOLOGICAL ADJUSTMENTS OF THE RADIAL NERVE ARE INTENSITY-DEPENDENT / AJUSTES MORFOLÓGICOS DO NERVO RADIAL SÃO DEPENDENTES DE INTENSIDADE / AJUSTES MORFOLÓGICOS DEL NERVIO RADIAL SON DEPENDIENTES DE INTENSIDAD

ABSTRACT Introduction: Peripheral nerve adaptation is critical for strength gains. However, information about intensity effects on nerve morphology is scarce. Objective: To compare the effects of different intensities of resistance training on radial nerve structures. Methods: Rats were divided into three groups: control (GC), training with 50% (GF1) and training 75% (GF2) of the animal’s body weight. The morphological analysis of the nerve was done by light and transmission electron microscopy. One-way ANOVA and the Tukey’s post hoc test were applied and the significance level was set at p≤0.05. Results: Training groups had an increase of strength compared to GC (p≤0.05). All measured nerve components (mean area and diameter of myelin fibers and axons, mean area and thickness of the myelin sheath, and of neurofilaments and microtubules) were higher in GF2 compared to the other (p≤0.05). Conclusion: Results demonstrated greater morphological changes on radial nerve after heavier loads. This can be important for rehabilitation therapies, training, and progression.

RESUMO Introdução: A adaptação dos nervos periféricos é fundamental para ganhos de força. No entanto, as informações relativas aos efeitos da intensidade sobre a morfologia do nervo são escassas. Objetivo: Comparar os efeitos de diferentes intensidades de treinamento de resistência sobre estruturas do nervo radial. Métodos: Os ratos foram divididos em três grupos: controle (GC) e treinamento com 50% (GF1) e 75% (GF2) do peso corporal do animal. A análise morfológica do nervo foi feita com microscopia óptica e eletrônica de transmissão. A one-way ANOVA e o teste post hoc de Tukey foram aplicados e o nível de significância foi estabelecido em p ≤ 0,05. Resultados: Os grupos treinamento tiveram aumento de força com relação ao GC (p ≤ 0,05). Todos os componentes medidos do nervo (área média e diâmetro de fibras de mielina e axônios, área média e espessura da bainha de mielina, neurofilamentos e microtúbulos) foram maiores no GF2 em comparação com os demais (p ≤ 0,05). Conclusão: Os resultados demonstraram maiores alterações morfológicas no nervo radial depois de cargas mais pesadas. Isso pode ser importante para terapias de reabilitação, treinamento e progressão.

RESUMEN Introducción: La adaptación de los nervios periféricos es fundamental para el aumento de fuerza. Sin embargo, la información sobre el efecto de la intensidad sobre la morfología del nervio es escasa. Objetivo: Comparar el efecto de diferentes intensidades de entrenamiento de resistencia en las estructuras del nervio radial. Métodos: Las ratas se dividieron en tres grupos: control (GC) y entrenamiento con 50% (GF1) y con 75% (GF2) del peso corporal del animal. El análisis morfológico del nervio se hizo con microscopía óptica y electrónica de transmisión. Se aplicaron la prueba ANOVA de una vía y la prueba post hoc de Tukey y el nivel de significación se fijó en p ≤ 0,05. Resultados: Los grupos de entrenamiento tuvieron aumento de la fuerza con respecto al grupo control (p ≤ 0,05). Todos los componentes medidos del nervio (área media y diámetro de las fibras de mielina y axones, área media y espesor de la vaina de mielina, neurofilamentos y microtúbulos) fueron mayores en GF2 en comparación con los otros grupos (p ≤ 0,05). Conclusión: Los resultados mostraron mayores cambios morfológicos en el nervio radial después de las cargas más pesadas. Esto puede ser importante para terapias de rehabilitación, entrenamiento y progresión.

Evaluation of Effective Transmission of Light Through Alveolar Bone: A Preliminary Study.

Introduction: The aim of the present study was to determine the effective transmission of 660 and 780 nm lasers through mandibular and maxillary alveolar bones in the buccal-lingual/ palatal direction. Methods: The laser probe was positioned in direct contact with the surface of the anterior, middle and posterior regions of each bone (5 dried maxillae and 5 mandibles) and the power meter was positioned on the bone wall opposite to the radiated wall for the measure of the remaining energy passing through the bone tissue. Ten measurements were performed with each laser at each irradiated point. Results: Transmitted power was significantly higher in bones irradiated with 780 nm laser. Tendencies toward greater average power transmitted in the anterior region of both bones at both wavelengths were also observed. Conclusion: Dosimetry and the choice of light source may be adjusted according to the anatomic region of the alveolar bone to be treated.

Measurement of effective remnant power in low intensity laser after passage through the buccinator muscle in anatomical human hemifaces / Determinação da potência efetiva remanescente após a passagem do laser de baixa intensidade através do músculo bucinador em peças anatômicas/hemifaces

Objective: To determine the effective remnant power after the passage of low intensity laser of two different wavelengths (660 and 780 nm) through buccinator muscle in anatomical hemifaces. Methods: Five human hemifaces were dissected, and a laser was shone in the central region of the muscle with a receiver placed on the opposite side. The hemifaces were irradiated using the same dosimetric parameters (40 mW, 1 W/cm2, continuous mode, 0.04 cm2) and at the same point in every muscle; remnant power was measured for each irradiation. Results: The average remnant power after irradiation with 660 nm (149 ± 15 µW) light was significantly lower (p<0.0001) than with that of 780 nm (380 ± 40 µW). Conclusion: The LIL of 780 nm presented greater remnant power in comparison to the 660 nm laser after passage through the buccinator muscle, indicating the latter ́s greater penetration capacity.

Objetivo: Determinar a potência remanescente após a passagem do laser de baixa intensidade em dois comprimentos de onda (660 e 780 nm) através do músculo bucinador em peças anatômicas dissecadas. Métodos: Dissecaram-se cinco hemifaces humanas expondo o músculo bucinador. Aplicou-se o laser na região central de cada músculo, e o receptor, para aferir a potência remanescente, foi posicionado na superfície intraoral contrária. As hemifaces foram irradiadas nos mesmos parâmetros dosimétricos (40 mW, 1 W/cm2, modo contínuo, 0,04 cm2) e no mesmo ponto em cada músculo, sendo a potência remanescente aferida a cada repetição. Resultados: A potência média restante após as irradiações de 660 nm (149 ± 15 µW) foi menor (p <0,0001) que com as irradiações de 780 nm (380 ± 40 µW). Conclusão: O LBI de 780 nm apresentou maior potência remanescente que o LBI de 660 nm, após passagem pelo músculo bucinador, denotando sua maior capacidade de penetração.

Effects of Dietary Supplementation with Agaricus sylvaticus Schaeffer on Glycemia and Cholesterol after Streptozotocin-Induced Diabetes in Rats.

This study evaluated the effect of the Agaricus sylvaticus (sun mushroom) on biochemical tests of the plasma and on the morphology of the pancreas in an experimental model of type I diabetes mellitus (DM1) induced by streptozotocin. One gram of dry A. sylvaticus was homogenized and mixed with the chow. Male Wistar rats were allocated as follows: normoglycemic control that received commercial chow; normoglycemic control group that received chow with A. sylvaticus; diabetic group that received commercial chow; and diabetic group that received chow with A. sylvaticus. Weight, food, and water consumption were measured every two days. Blood glucose levels were measured twice a week. After 30 days, the animals were euthanized and blood was collected for the analysis of cholesterol, HDL, triglycerides, blood sugar, glutamic-pyruvic transaminase (GPT), alkaline phosphatase, iron, transferrin, and urea. The pancreas was processed for microscopic analysis. A. sylvaticus modulated the levels of cholesterol, HDL, triglycerides, blood sugar, GPT, alkaline phosphatase, iron, transferrin, and urea to levels similar to those found in the controls and led to compensatory hyperplasia of the islets of Langerhans. A. sylvaticus is potentially beneficial in the control of type 1 diabetes, and it may also prevent pancreas damage.

Immunohistochemical expression of biglycan and decorin in the pulp tissue of human primary teeth during resorption.

Primary teeth are interesting models that can be used to study physiological and pathological processes involving cells and extracellular matrices in hard and soft tissues. This study investigated the expression and distribution of biglycan and decorin-the non-collagenous components of the extracellular matrix-in primary teeth tissue, during physiological root resorption. Thirty healthy human primary teeth were grouped together according to root length: Group I - two-thirds root length, Group II - one-third root length, and Group III - teeth with no root. The streptavidin-biotin-peroxidase immunohistochemical method was used with antibodies against the previously named antigens. The proteoglycans studied were found in the pulp and dentin extracellular matrix in all groups without any differences in the proteins, among the groups. Biglycan was observed mainly in predentin and in pulp connective tissue in the resorption area. In addition, decorin was observed mainly in pulp connective tissue, but near the resorption area. Biglycan and decorin were distributed differentially in the dental tissues. The present immunohistocytochemical data, combined with previously reported data, suggest that these proteoglycans could be involved in regulating the physiological resorption process in healthy primary teeth.

Immunohistochemical expression of biglycan and decorin in the pulp tissue of human primary teeth during resorption

Primary teeth are interesting models that can be used to study physiological and pathological processes involving cells and extracellular matrices in hard and soft tissues. This study investigated the expression and distribution of biglycan and decorin-the non-collagenous components of the extracellular matrix-in primary teeth tissue, during physiological root resorption. Thirty healthy human primary teeth were grouped together according to root length: Group I - two-thirds root length, Group II - one-third root length, and Group III - teeth with no root. The streptavidin-biotin-peroxidase immunohistochemical method was used with antibodies against the previously named antigens. The proteoglycans studied were found in the pulp and dentin extracellular matrix in all groups without any differences in the proteins, among the groups. Biglycan was observed mainly in predentin and in pulp connective tissue in the resorption area. In addition, decorin was observed mainly in pulp connective tissue, but near the resorption area. Biglycan and decorin were distributed differentially in the dental tissues. The present immunohistocytochemical data, combined with previously reported data, suggest that these proteoglycans could be involved in regulating the physiological resorption process in healthy primary teeth.

Distribution of urocortin 3 neurons innervating the ventral premammillary nucleus in the rat brain.

Urocortin 3 (Ucn 3) is a recently described peptide of the corticotropin-releasing factor family. Neurons expressing Ucn 3 mRNA and peptide are distributed in specific brain areas, including the median preoptic nucleus, the perifornical area (PFx), and the medial nucleus of the amygdala (MEA). Fibers immunoreactive to Ucn 3 are confined to certain brain nuclei, being particularly dense in the ventral premammillary nucleus (PMV). In studies involving electrolytic lesions and analysis of Fos distribution according to behavioral paradigms, the PMV has been potentially implicated in conspecific aggression and sexual behavior. However, the role that Ucn 3 plays in this pathway has not been explored. Therefore, we investigated the origins of the urocortinergic innervation of the PMV of Wistar rat in an attempt to map the brain circuitry and identify likely related functions. We injected the retrograde tracer cholera toxin b subunit into the PMV and found that 88% of the Ucn 3-immunoreactive fibers in the PMV originate in the dorsal MEA, and that few originate in the PFx. As a control, we injected the anterograde tracer biotin dextran amine into both regions. We observed that the PMV is densely innervated by the MEA, and scarcely innervated by the PFx. The MEA is a secondary relay of the vomeronasal system and projects amply to hypothalamic nuclei related to hormonal and behavioral adjustments, including the PMV. Although physiological studies should also be performed, we hypothesize that Ucn 3 participates in such pathways, conveying sensory information to the PMV, which in turn modulates behavioral and neuroendocrine responses.

Alternative pathways for catecholamine action in oral motor control.

Orofacial movement is a complex function performed by facial and jaw muscles. Jaw movement is enacted through the triggering of motoneurons located primarily in the trigeminal motor nucleus (Mo5). The Mo5 is located in the pontine reticular formation, which is encircled by premotor neurons. Previous studies using retrograde tracers have demonstrated that premotor neurons innervating the Mo5 are distributed in brainstem areas, and electrophysiological studies have suggested the existence of a subcortical relay in the corticofugal-Mo5 pathway. Various neurotransmitters have been implicated in oral movement. Dopamine is of special interest since its imbalance may produce changes in basal ganglia activity, which generates abnormal movements, including jaw motor dysfunction, as in oral dyskinesia and possibly in bruxism. However, the anatomical pathways connecting the dopaminergic systems with Mo5 motoneurons have not been studied systematically. After injecting retrograde tracer fluorogold into the Mo5, we observed retrograde-labeled neurons in brainstem areas and in a few forebrain nuclei, such as the central nucleus of the amygdala, and the parasubthalamic nucleus. By using dual-labeled immunohistochemistry, we found tyrosine hydroxylase (a catecholamine-processing enzyme) immunoreactive fibers in close apposition to retrograde-labeled neurons in brainstem nuclei, in the central nucleus of the amygdala and the parasubthalamic nucleus, suggesting the occurrence of synaptic contacts. Therefore, we suggested that catecholamines may regulate oralfacial movements through the premotor brainstem nuclei, which are related to masticatory control, and forebrain areas related to autonomic and stress responses.