Early-Life Blockade of 5-HT1A Receptors Alters Adult Anxiety Behavior and Benzodiazepine Sensitivity

BackgroundEarly-life stress may affect 5-HT1A receptor circuitry, which could result in increased anxiety in later life. An increased anxiety phenotype in 5-HT1A receptor KO mice (1AKO) mice has been ascribed to 5-HT1A receptor absence during the early postnatal period. Thus, subtle and transient serotonergic changes during the early postnatal period may lead to an increased risk for developing stress-related disorders during adulthood.MethodsWildtype and 1AKO mice on a Swiss-Webster (SW) background were treated during the early postnatal period with vehicle or the 5-HT1A receptor antagonist WAY-100,635.ResultsPharmacologic 5-HT1A receptor blockade during the early postnatal period induced long-lasting effects on anxiety and benzodiazepine sensitivity in adolescent and adult mice on a Swiss-Webster background and resembles the SW 1AKO phenotype. Furthermore, WAY-100,635-treated mice had increased cortical gamma-aminobutyric acid-A receptor (GABAAR) α1 and α3 subunit levels and increased hippocampal GABAAR α2 subunit levels.ConclusionsAbsence of 5-HT1AR signaling during early stages of brain maturation predisposes an organism to affective dysfunction later in life. Because early-life treatment with WAY-100,635 in Swiss-Webster mice reduced diazepam sensitivity and increased GABAAR α subunit levels in the prefrontal cortex and hippocampus, our data suggest a putative link between early-life disruption of the serotonergic system and the emergence of increased anxiety and decreased benzodiazepine responsivity at adult age. Moreover, early-life 5-HT1A receptor functionality appears to be essential for the development of normal GABAAR functionality. This study may have clinical implications for psychoactive drug use during pregnancy and for the pharmacogenetic background of benzodiazepine sensitivity.