Prenatal exposure to vortioxetine and vilazodone: Impact on depressive- and anxiety-like behavioral manifestations in young rat offspring

• Published in: Behavioural brain research 2024-08, Vol.471, p.115128, Article 115128
• Main Authors: Singh, Pallavi, Agrawal, Priyanka, Singh, K.P.
• Format: Article
• Language: English
• Subjects: Animals; Antidepressive Agents - pharmacology; Anxiety; Anxiety - chemically induced; Behavior, Animal - drug effects; Depression; Depression - chemically induced; Depression - drug therapy; Disease Models, Animal; Dopamine; Female; Male; Pregnancy; Prenatal Exposure Delayed Effects - chemically induced; Rats; Rats, Wistar; Serotonin; Vilazodone; Vilazodone Hydrochloride - pharmacology; Vortioxetine; Vortioxetine - pharmacology
• ISSN: 0166-4328; 1872-7549; 1872-7549
• DOI: 10.1016/j.bbr.2024.115128

Major depressive disorder (MDD) affects millions of people worldwide, with women at a higher risk during the childbearing age. Vortioxetine (VOX) and Vilazodone (VLZ) are newer antidepressants with improved therapeutic profile commonly used, but their safety during pregnancy and long-term effects on offspring are poorly understood due to paucity of literature in preclinical and clinical studies. This study aimed to investigate whether prenatal exposure to VOX and VLZ impacts depressive- and anxiety-like neurobehavioral alterations in offspring, focusing on neurotransmitter-mediated mechanisms. Pregnant Wistar dams received either VOX or VLZ, 1 mg/day and 2 mg/day of the drug orally from gestation day (GD) 6–21. The dams naturally delivered their offspring and reared until they reached postnatal day (PND) 21. Offspring of both sexes were tested for display of depressive-and anxiety-like behaviors from PND 56–70. After PND 70, offspring were sacrificed, and their brains were collected to estimate neurotransmitter levels. As per protocol, controls were maintained simultaneously for each experimental design. Prenatal exposure to VOX or VLZ induced an increased state of depressive- and anxiety-like behaviors in both male and female offspring. Additionally, neurotransmitter (serotonin, dopamine, and nor-epinephrine) levels in the prefrontal cortex region of the brain were substantially reduced in exposed offspring. No sex specific neurobehavioral and neurochemical implications were observed in the present study. Our findings suggest that prenatal exposure to VOX and VLZ disrupts neurochemical balance in the fetal brain, leading to long-lasting neurobehavioral impairments in offspring of both sexes. •Vortioxetine or vilazodone prenatal exposure increased depressive-like behaviors.•Anxiety-like behaviors also elevated in exposed offspring.•Serotonin level decline in prefrontal cortex of offspring’s brain.•No significant difference observed on gender basis.