ABSTRACT
ABSTRACT Objective To evaluate, in rat offspring, bone changes induced by excess maternal thyroxin during pregnancy and lactation, and to assess the reversibility of these changes after weaning. Material and methods Twenty Wistar rats were distributed in two groups, hyperthyroid and control, that were treated daily with L-thyroxin (50 mcg/animal) and placebo, respectively. The treatment was initiated seven days before mating and continued throughout pregnancy and lactation. From every female of each of the two groups, two offspring were euthanized after birth, two at 21 days of age (weaning), and two at 42 days of age (21 days after weaning). In newborns, the length of pelvic and thoracic limbs were measured, and in the other animals, the length and width of the femur and humerus were measured. Bones were dissected, decalcified, embedded in paraffin, and analyzed histomorphometrically. Results Excess maternal thyroxin significantly reduced the length of the pelvic limb in neonates. In 21-day-old individuals, excess maternal thyroxine reduced the length and the width of the femur and the humerus. It also increased thickness of the epiphyseal plate and the percentage of trabecular bone tissue. In 42-day-old individuals, there were no significant differences between groups in relation to the parameters evaluated in the previous periods. Conclusion Excess maternal thyroxine reduced growth in suckling rats both at birth and at weaning, and it also increased the percentage of trabecular bone tissue in 21-day-old animals. These changes, however, were reversible at 42 days, i.e., 21 days after weaning. Arch Endocrinol Metab. 2016;60(2):130-7.
Subject(s)
Animals , Male , Female , Pregnancy , Thyroxine/pharmacology , Bone and Bones/drug effects , Bone and Bones/pathology , Maternal-Fetal Exchange , Thyroxine/metabolism , Time Factors , Weaning , Bone and Bones/metabolism , Lactation/drug effects , Age Factors , Rats, Wistar , Animals, Newborn/growth & developmentABSTRACT
OBJETIVO: Avaliar as diferenças sítio-ósseo dependentes no efeito das disfunções tireoidianas no fêmur e vértebras lombares de ratas. MÉTODOS: 33 ratas Wistar com dois meses de idade foram distribuídas em três grupos: eutireoideas (controle), hipotireoideas e hipertireoideas. Após 90 dias de tratamento para indução do hipo e hipertireoidismo, as ratas foram eutanasiadas, o sangue foi colhido para dosagem de T4 livre e os fêmures e as vértebras lombares (L1-L3) foram descalcificados e processados para análise da porcentagem de tecido ósseo trabecular. RESULTADOS: O grupo hipertireoideo apresentou porcentagem de tecido ósseo trabecular significativamente mais elevada na metáfise femoral, em comparação ao controle. Mas o hipertireoidismo não alterou a porcentagem de tecido ósseo trabecular na vértebra. O hipotireoidismo reduziu significativamente a porcentagem de tecido ósseo trabecular em comparação aos demais grupos nos segmentos 1-3 das vértebras lombares, mas não alterou a porcentagem de tecido ósseo trabecular no fêmur. CONCLUSÃO: O efeito do hipotireoidismo e do hipertireoidismo sobre a histomorfometria óssea é diferente e dependente do sítio ósseo.
OBJECTIVE: Evaluating bone site-dependent differences in the effect of thyroid dysfunctions on the femur and lumbar vertebrae of female rats. METHODS: Thirty-three 2-month-old female wistar rats were distributed in three groups: euthyroid (control), hypothyroid and hyperthyroid. Ninety days after treatment for hypothyroidism and hyperthyroidism induction, the female rats were euthanized; the blood was collected for free T4 dosage and the femurs and segment 1-3 of the lumbar vertebrae were decalcified and processed for analysis of the trabecular bone percentage. RESULTS: The hyperthyroid group showed significantly higher trabecular bone percentage in the femoral metaphysis, in comparison with the control group. But the hyperthyroidism group did not increase the trabecular bone percentage in the lumbar vertebrae. The hypothyroidism group significantly reduced the trabecular bone percentage in the lumbar vertebrae, but did not alter the trabecular bone percentage in the femur. CONCLUSION: The effect of hypothyroidism and hyperthyroidism on bone histomorphometry is different in each condition and bone site-dependent.