Developmental Fluoxetine Exposure Alters Behavior and Neuropeptide Receptors in the Prairie Vole

Autor: Rebecca H. Lawrence, Michelle C. Palumbo, Sara M. Freeman, Caleigh D. Guoynes, Karen L. Bales
Rok vydání: 2020
Předmět:
serotonin receptor
medicine.medical_specialty
Vasopressin
Oxytocin receptor binding
Intellectual and Developmental Disabilities (IDD)
Cognitive Neuroscience
Serotonin reuptake inhibitor
5-HT
autism
Biology
Basic Behavioral and Social Science
autoradiography
lcsh:RC321-571
03 medical and health sciences
Behavioral Neuroscience
0302 clinical medicine
Internal medicine
Behavioral and Social Science
medicine
Psychology
vasopressin receptor
SSRI
lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry
5-HT receptor
Original Research
030304 developmental biology
Vasopressin receptor
Pediatric
0303 health sciences
antidepressant
Depression
Neurosciences
Perinatal Period - Conditions Originating in Perinatal Period
biology.organism_classification
Oxytocin receptor
Brain Disorders
Prairie vole
oxytocin receptor
Mental Health
Neuropsychology and Physiological Psychology
Endocrinology
Oxytocin
Cognitive Sciences
030217 neurology & neurosurgery
Neuroscience
medicine.drug
Zdroj: Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience, Vol 14 (2020)
ISSN: 1662-5153
DOI: 10.3389/fnbeh.2020.584731
Popis: Developmental exposure to selective serotonin reuptake inhibitor (SSRI) increases the risk of Autism Spectrum Disorder (ASD), however, the underlying neurobiology of this effect is not fully understood. Here we used the socially monogamous prairie vole as a translational model of developmental SSRI exposure. Paired female prairie voles (n = 20) were treated with 5 mg/kg subcutaneous fluoxetine (FLX) or saline (SAL) daily from birth of the second litter until the day of birth of the 4th litter. This design created three cohorts of FLX exposure: postnatal exposure in litter 2, both prenatal and postnatal exposure in litter 3, and prenatal exposure in litter 4. Post-weaning, subjects underwent behavioral testing to detect changes in sociality, repetitive behavior, pair-bond formation, and anxiety-like behavior. Quantitative receptor autoradiography was performed for oxytocin, vasopressin 1a, and serotonin 1a receptor density in a subset of brains. We observed increased anxiety-like behavior and reduced sociality in developmentally FLX exposed adults. FLX exposure decreased oxytocin receptor binding in the nucleus accumbens core and central amygdala, and vasopressin 1a receptor binding in the medial amygdala. FLX exposure did not affect serotonin 1A receptor binding in any areas examined. Changes to oxytocin and vasopressin receptors may underlie the behavioral changes observed and have translational implications for the mechanism of the increased risk of ASD subsequent to prenatal SSRI exposure.
Databáze: OpenAIRE