ABSTRACT
The Phrynops hilarii specie of turtle has its characterization not well defined in the literature, it was proposed in this study the leukocyte characterization of the blood, stained by Leishman and analyzed under light and transmission electron microscope. It was not observe any cellular type with similar characteristics to neutrophils in mammalian group. We believed, based on the data obtained in this study that the heterophils have a morphofuncional analogy with another neutrophils belonged to mammalian group. This conclusion is being supported in many recent studies found in the literature.
La especie de tortuga Phrynops hilarii no ha sido aún bien descrita en la literatura. Fue propuesto en este estudio la caracterización de leucocitos de sangre de este animal coloreados con el método de Leishman y analizados con microscopías de luz y electrónica. No fue observado ningún tipo celular con características similares a los neutrófilos de mamíferos. Los resultados indican que los heterófilos tienen analogía morfofuncional con otros neutrófilos presentes en el grupo de los mamíferos. Esta conclusión es sustentada por varios estudios recientes encontrados en la literatura.
ABSTRACT
The aim of this study was to show the microwaves action in fixation of rat fetuses, dermal and cartilaginous tissues, using histological and immunohistochemistry methods for analysis. It was possible to conclude in this study using the rat as experimental model that the two methods for antibody retrieval, presented an excellent ways for the use of Ki67 antibody in the immunohistochemical analysis.
El objetivo de este estudio fue evaluar la acción de las microondas en la fijación de los tejidos dérmico y cartilaginoso de fetos de ratas, usando para el análisis métodos histológico e inmunohistoquímico. Fue posible concluir en este estudio usando la rata como modelo experimental, que los dos métodos empleados para la recuperación antigénica representan excelentes medios para el uso del anticuerpo Ki67, en el análisis inmunohistoquímico.
ABSTRACT
The localization of peroxidase activity in different cell regions is used as a criterion for the classification of the stage of maturation of mammalian mononuclear phagocytes with a positive peroxidase reaction indicating the presence of monoblasts, promonocytes, monocytes and macrophages. In this study it was evaluated the peroxidase activity of blood mononuclear phagocytes of this turtle detected at different stages of differentiation. The present observations suggest that, in turtles, the differentiation of mononuclear phagocytes occur in the blood circulation, in contrast to animals, where only are monocytes in circulating blood and macrophage differentiation occurs in other body compartments.
La localization de la actividad de la peroxidasa en diversas regiones de la célula se utiliza como criterio para la clasificación de la etapa de maduración de fagocitos mononucleares. Una reacción positiva de peroxidasa indica la presencia de monoblastos, promonocitos, monocitos y macrófagos. En este estudio fue evaluada la actividad de la peroxidasa de los fagocitos mononucleares de la sangre de la tortuga Phrynops Hilarii detectada en diversas etapas de la diferenciación. Las actuales observaciones sugieren que, en tortugas, la diferenciación de fagocitos mononucleares ocurre en la circulación de la sangre, en contraste a los mamíferos, donde están solamente los monocitos en la sangre circulante y la diferenciación de los macrófagos ocurre en otras partes del cuerpo.
Subject(s)
Animals , Blood , Phagocytes/enzymology , Macrophages/enzymology , Peroxidases/metabolism , TurtlesABSTRACT
The aim of this article is to present the decalcification process dynamic of mineralized tissue in dogs, teeth and jaw, comparing the traditional decalcification method, immersion, and microwave, immersion followed by irradiation using a domestic microwave oven, accompanying the liberation of calcium through spectrophotometer of atomic absorption. It was used as decalcified agent, EDTA solution or nitric acid. The results showed that with the use of nitric acid (5 percent), after 15 days, the irradiated fragments could be processed for histological analysis, otherwise the tooth not irradiated need to be submerged for 65 days. The EDTA decalcified action was slower than the nitric acid. The histological observations of the irradiated samples showed an excellent preservation of the morphological characteristics, independently of the decalcified agent used.
El objetivo de este artículo fue presentar, un método de descalcificación dinámico de tejido mineralizado de perros, dientes y mandíbula, comparando el método de descalcificación tradicional e irradiación en horno de microondas, analizando la liberación de calcio en espectro fotómetro de absorción atómica. Usamos como agente descalcificante, solución de EDTA y acido nítrico. Los resultados mostraron que los fragmentos descalcificados con ácido nítrico después de 15 días, ya podían ser preparados para análisis histológico, el diente al ser irradiado tardó 65 días para ser descalcificado. El EDTA descalcificó lentamente, en relación al ácido nítrico. Las observaciones histológicas de las muestras irradiadas mostraron una excelente preservación de las características morfológicas independiente del agente descacificador usado.
Subject(s)
Animals , Dogs , Nitric Acid/administration & dosage , Bone Demineralization Technique/methods , MicrowavesABSTRACT
Bone decalcification is a time-consuming process. It takes weeks and preservation of the tissue structure depends on the quality and velocity of the demineralization process. In the present study, a decalcification methodology was adapted using microwaving to accelerate the decalcification of rat bone for electron microscopic analysis. The ultrastructure of the bone decalcified by microwave energy was observed. Wistar rats were perfused with paraformaldehyde and maxillary segments were removed and fixed in glutaraldehyde. Half of specimens were decalcified by conventional treatment with immersion in Warshawsky solution at 4ºC during 45 days, and the other half of specimens were placed into the beaker with 20 mL of the Warshawsky solution in ice bath and thereafter submitted to irradiation in a domestic microwave oven (700 maximum power) during 20 s/350 W/±37ºC. In the first day, the specimens were irradiated 9 times and stored at 40ºC overnight. In the second day, the specimens were irradiated 20 times changing the solution and the ice after each bath. After decalcification, some specimens were postfixed in osmium tetroxide and others in osmium tetroxide and potassium pyroantimonate. The specimens were observed under transmission electron microscopy. The results showed an increase in the decalcification rate in the specimens activated by microwaving and a reduction of total experiment time from 45 days in the conventional method to 48 hours in the microwave-aided method.
A preservação da estrutura de ossos é dependente da qualidade e da velocidade em que ocorre o processo de desmineralização. Neste estudo foi observada a ultraestrutura de maxila de rato descalcificada utilizando microondas. Ratos Wistar sofreram perfusão com paraformaldeído e o segmento de maxila retirado e fixado em glutaraldeído. Após esta etapa algumas amostras foram descalcificadas por imersão em solução de Warshawsky durante 45 dias a 4(0)C. Outras amostras foram submetidas a irradiação por microondas (forno de microondas doméstico 700 Watts de potência), durante 20 s/350 W/ ± 37ºC. No primeiro dia foram realizadas um total de 9 irradiações e os espécimes foram deixadas posteriormente a 4ºC por 12 h na solução descalcificadora sem agitação. No segundo dia, os fragmentos foram submetidos à nova irradiação totalizando 20 banhos, trocando-se a solução e o gelo a cada banho. A seguir algumas amostras foram pós-fixadas com tetróxido de ósmio e outras com tetróxido de ósmio e piroantimonato de potássio. As amostras foram observadas em microscópio eletrônico de transmissão. Os resultados mostraram que o processo de descalcificação ativado por microondas reduziu para 48 h o período de descalcificação, o qual pelo método tradicional ocorre em 45 dias.