Department of Psychiatry, Columbia University Medical Center, New York, United States; Division of Developmental Neuroscience, New York State Psychiatric Institute, New York, United States
Emma S Holt
Division of Developmental Neuroscience, New York State Psychiatric Institute, New York, United States
Laura J Benoit
Department of Psychiatry, Columbia University Medical Center, New York, United States; Division of Molecular Therapeutics, New York Psychiatric Institute, New York, United States
Eric Teboul
Division of Molecular Therapeutics, New York Psychiatric Institute, New York, United States
Gabriella M Sahyoun
Division of Developmental Neuroscience, New York State Psychiatric Institute, New York, United States
R Todd Ogden
Department of Biostatistics, Mailman School of Public Health, Columbia University Medical Center, New York, United States
Department of Psychiatry, Columbia University Medical Center, New York, United States; Division of Integrative Neuroscience, New York State Psychiatric Institute, New York, United States
Department of Psychiatry, Columbia University Medical Center, New York, United States; Division of Molecular Therapeutics, New York Psychiatric Institute, New York, United States; Department of Molecular Pharmacology & Therapeutics, Columbia University Medical Center, New York, United States
In their seminal findings, Hubel and Wiesel identified sensitive periods in which experience can exert lasting effects on adult visual cortical functioning and behavior via transient changes in neuronal activity during development. Whether comparable sensitive periods exist for non-sensory cortices, such as the prefrontal cortex, in which alterations in activity determine adult circuit function and behavior is still an active area of research. Here, using mice we demonstrate that inhibition of prefrontal parvalbumin (PV)-expressing interneurons during the juvenile and adolescent period, results in persistent impairments in adult prefrontal circuit connectivity, in vivo network function, and behavioral flexibility that can be reversed by targeted activation of PV interneurons in adulthood. In contrast, reversible suppression of PV interneuron activity in adulthood produces no lasting effects. These findings identify an activity-dependent sensitive period for prefrontal circuit maturation and highlight how abnormal PV interneuron activity during development alters adult prefrontal circuit function and cognitive behavior.