Author/Authors :
M?rio Oliveira، نويسنده , , Jo?o M. Bessa، نويسنده , , Ana Mesquita، نويسنده , , Hugo Tavares، نويسنده , , André Carvalho، نويسنده , , Rui Silva، نويسنده , , José M. Pêgo، نويسنده , , Jo?o J. Cerqueira، نويسنده , , Joana A. Palha، نويسنده , , Osborne F.X. Almeida، نويسنده , , Nuno Sousa، نويسنده ,
Abstract :
Background
Synthetic glucocorticoids are commonly prescribed during pregnancy, despite a lack of systematic investigations of their potential impact on the developing brain and neurological and behavioral performance.
Methods
Neuroendocrine parameters and behavior in the adult offspring of pregnant Wistar rats treated antenatally with either dexamethasone (DEX) or corticosterone (CORT) were monitored; DEX (.1 mg/kg and 1 mg/kg) and CORT (25 mg/kg) were given to pregnant rat dams on gestation days 18 and 19.
Results
Despite normal basal levels of corticosterone, the adult offspring of mothers given DEX or CORT displayed abnormal responses in the dexamethasone-suppression test. Neither treatment influenced spatial memory performance, but both DEX and CORT facilitated development of depressionlike behavior following chronic stress. The latter finding demonstrates that high-dose antenatal corticotherapy can impair the organism’s resilience to stress in adulthood. Interestingly, comparison of the progeny of CORT-treated and DEX-treated mothers revealed that the latter were more anxious.
Conclusions
Since DEX and CORT differ in their affinity for glucocorticoid and mineralocorticoid receptors and corticosteroid-binding globulin, our findings emphasize the need to consider the pharmacologic properties of antenatal corticotherapies and demonstrate the potential long-term benefits of ligands that can bind to both receptors.
Keywords :
neurodevelopment , Anxiety , corticosteroids , depression , antenatal corticotherapy , cognition