ABSTRACT
In two different experiments, the effects of hyperthyroidism on the histomorphometry and expression of Cdc47 and caspase-3 were evaluated in the uteri and placentas during gestation and postpartum. Fetal development was also evaluated during gestation. In the first experiment, 36 adult female Wistar rats were divided into two groups of 18 animals each: (1) hyperthyroid; and (2) euthyroid (control). Female rats were mated and killed at 7, 14 and 19 days of gestation. Uteri and placentas were weighed and subjected to histomorphometric and immunohistochemical evaluation to determine the expression of Cdc47 and caspase-3. Ovaries were also evaluated for weight and subjected to morphometric analysis. Fetuses were quantified and weighed individually. In the second experiment, 12 adult female Wistar rats were divided into two groups of six animals each: (1) hyperthyroid; and (2) euthyroid (control). Female rats were mated and killed 2 days postpartum. Uteri were evaluated in the same way as for the first experiment. Hyperthyroidism increased ovulation and conception rates without disturbing the size and viability of the fetuses. In the pregnant uteri, hyperthyroidism did not change the thickness of the layers or the expression of Cdc47 and caspase-3. However, in the placentas, hyperthyroidism increased the medium diameter of trophoblast cells, as well as the thickness and the expression of Cdc47 of spongiotrophoblast cells, at 14 days of gestation. During uterine involution, hyperthyroidism significantly increased the expression of Cdc47 and reduced the expression of caspase-3 in the uterine layers. In conclusion, hyperthyroidism increased the conception rate because of an ovulation gain, induced significant placental changes during pregnancy and, in the uterus, increased Cdc47 expression and decreased caspase-3 expression after parturition.
Subject(s)
Adenosine Triphosphatases/metabolism , Caspase 3/metabolism , DNA-Binding Proteins/metabolism , Fetal Development , Hyperthyroidism/metabolism , Placenta/metabolism , Postpartum Period/metabolism , Pregnancy Complications/metabolism , Uterus/metabolism , Adenosine Triphosphatases/analysis , Animals , Caspase 3/analysis , DNA-Binding Proteins/analysis , Female , Immunohistochemistry , Minichromosome Maintenance Complex Component 7 , Placenta/chemistry , Placenta/pathology , Pregnancy , Rats , Rats, Wistar , Uterus/chemistry , Uterus/pathologyABSTRACT
The main purpose of this study was to investigate the effect of thyroxine and PTU in ascitic Ehrlich tumor cells. Tumor was implanted in 30 female mice distributed in three groups: treated with PTU, treated with thyroxine and control. Each group received an intraperitoneal injection of neoplastic cells, pre-incubated with sterile solutions of PTU, thyroxine and distilled water, respectively. On the fifth and seventh days after inoculation, animals received an intraperitoneal injection of the respective solutions. On the tenth day after inoculation, animals were sacrificed. Volume of ascitic liquid, number of neoplastic cells/ml and percentage of viable cells were determined. Ascitic liquid smears were carried out for tumor cytological evaluation. There was no difference among groups regarding ascitic liquid and as for the number and viability of tumor cells. However, cells under the effect of thyroxine presented significantly larger mean of nuclear diameter, size and number of nucleolus organizer regions. In this group, there was a predominance of clear, round cells with abundant eosinophilic and very vacuolated cytoplasm with little defined edges. Under the PTU effect, tumor cells were small with hyperchromatic nucleus and the same number of NORs as the control group. It was concluded that PTU and thyroxine have not changed the number and viability of cells after 10 days of tumor inoculation but they changed significantly cell characteristics. Whilst thyroxine increases cell size and the number of NORs of ascitic Ehrlich tumor cells, PTU causes an opposite effect.
El propósito principal de este estudio ha sido investigar el efecto de la tiroxina y del propiltiouracilo (PTU) en las células del tumor de Ehrlich. El tumor fue implantado en 30 ratones hembras distribuidas en tres grupos: tratado con PTU, tratado con tiroxina y control. Cada grupo recibió una inyección intraperitoneal de células neoplásicas, pre-incubadas con las soluciones estériles de PTU, tiroxina y agua, respectivamente. En el quinto y séptimo días después de la inoculación, los animales recibieron una inyección intraperitoneal de las soluciones respectivas. En el décimo día después de la inoculación, se sacrificaron los animales. Fueron determinados el volumen de líquido ascítico, el número de células/ml y el porcentaje de células viables. Además se realizaron frotis del líquido ascítico para la evaluación de la citología del tumor. No hubo ninguna diferencia entre los grupos con respecto al volumen del líquido ascítico y el número y viabilidad de las células del tumor. Sin embargo, las células bajo el efecto de la tiroxina presentaron una media significativamente superior del diámetro nuclear, tamaño y número de regiones organizadoras de nucleélos. En este grupo, había un predominio de células claras, redondas con citoplasma abundante, eosinofílico y vacuolado con poca definición de los bordes. Bajo el efecto del PTU, las células del tumor eran pequeñas con el núcleo hipercromático y el mismo número de NORs como el grupo control. Se concluye que el PTU y tiroxina no afectaron el número y viabilidad de las células después de 10 días de inoculación del tumor, pero sí cambiaron las características celulares. Aunque la tiroxina aumenta el tamaño celular y el número de NORs de las celulas del tumor de Ehrlich, PTU causa efectos opuestos.