Revisiting the role of infralimbic cortex in fear extinction with optogenetics.

Kelvin Quiñones-Laracuente's picture
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TitleRevisiting the role of infralimbic cortex in fear extinction with optogenetics.
Publication TypeJournal Article
Year of Publication2015
AuthorsDo-Monte, FH, Manzano-Nieves, G, Quiñones-Laracuente, K, Ramos-Medina, L, Quirk, GJ
JournalJ Neurosci
Volume35
Issue8
Pagination3607-15
Date Published2015 Feb 25
ISSN1529-2401
KeywordsAction Potentials, Amygdala, Animals, Conditioning, Classical, Extinction, Psychological, Fear, Glutamic Acid, Male, Neurons, Optogenetics, Prefrontal Cortex, Rats, Rats, Sprague-Dawley
Abstract

Previous rodent studies have implicated the infralimbic (IL) subregion of the medial prefrontal cortex in extinction of auditory fear conditioning. However, these studies used pharmacological inactivation or electrical stimulation techniques, which lack temporal precision and neuronal specificity. Here, we used an optogenetic approach to either activate (with channelrhodopsin) or silence (with halorhodopsin) glutamatergic IL neurons during conditioned tones delivered in one of two phases: extinction training or extinction retrieval. Activating IL neurons during extinction training reduced fear expression and strengthened extinction memory the following day. Silencing IL neurons during extinction training had no effect on within-session extinction, but impaired the retrieval of extinction the following day, indicating that IL activity during extinction tones is necessary for the formation of extinction memory. Surprisingly, however, silencing IL neurons optogenetically or pharmacologically during the retrieval of extinction 1 day or 1 week following extinction training had no effect. Our findings suggest that IL activity during extinction training likely facilitates storage of extinction in target structures, but contrary to current models, IL activity does not appear to be necessary for retrieval of extinction memory.

DOI10.1523/JNEUROSCI.3137-14.2015
Alternate JournalJ. Neurosci.
PubMed ID25716859
PubMed Central IDPMC4339362
Grant ListP50-MH086400 / MH / NIMH NIH HHS / United States
R01-MH081975 / MH / NIMH NIH HHS / United States
R25 GM061838 / GM / NIGMS NIH HHS / United States
R25-GM061151 / GM / NIGMS NIH HHS / United States
R25-GM061838 / GM / NIGMS NIH HHS / United States
R37 MH058883 / MH / NIMH NIH HHS / United States
R37-MH058883 / MH / NIMH NIH HHS / United States