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Fear conditioning and extinction generate conflicting memory representations for a conditioned stimulus (CS). Retrieval of either memory is largely determined by the context where the CS is encountered. While fear typically generalizes to CSs encountered in new contexts, extinction is specific to the environment in which it was learned. Here, we used an fMRI design (n = 30, 16 women) to tag and track the extent to which individual participants reinstated competing episodic mental contexts associated with threat conditioning and extinction. We examined whether reactivation of past encoding contexts influences threat expectancy behavior and neural responses to a threat-ambiguous CS encountered in a new context. Results showed that the relative balance between conditioning and extinction context reinstatement in higher-order visual cortex influenced threat expectancy and neural activity in canonical threat processing regions. The link between context reinstatement and fear-related processes was specific to an extinguished CS, as opposed to an unextinguished CS that had never been encountered in the extinction context. These effects were observed 24 hr later, but not after 3 weeks. Additionally, threat conditioning produced long-lasting changes in primary sensory cortex that persisted up to 3 weeks following extinction. These findings show that neural representations of threat can endure over long durations, even in the healthy brain. Our results indicate competition between divergent mental contexts determines feelings of danger or safety when the meaning of the CS is ambiguous and suggest a mechanism by which the brain resolves ambiguity by reinstating the more dominant context associated with either fear or extinction.
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http://dx.doi.org/10.1162/jocn.a.93 | DOI Listing |
J Exp Anal Behav
September 2025
Laboratorio de Análisis de la Conducta, Universidad Nacional Autónoma de México. Facultad de Estudios Superiores Iztacala.
Rules can control the listener's behavior, yet few studies have examined variables that quantitatively determine the extent of this control relative to other rules and contingencies. To explore these variables, we employed a novel procedure that required a choice between rules. Participants clicked two buttons on a computer screen to earn points exchangeable for money.
View Article and Find Full Text PDFDev Psychobiol
September 2025
Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Social buffering may reduce the persistent impacts of acute early life stress (aELS) and, thus, has important implications for anxiety- and trauma-related disorders. First, we assessed whether aELS would induce maladaptive fear incubation in adult mice, a PTSD-like phenotype. Overall, animals showed incubation of fear memory in adulthood, independent of aELS condition.
View Article and Find Full Text PDFJ Exp Anal Behav
September 2025
Utah State University, Logan, UT, USA.
Discontinuing reinforcement for an operant behavior sometimes produces a transient increase in responding (i.e., an extinction burst).
View Article and Find Full Text PDFDev Psychobiol
September 2025
School of Psychology, UNSW Sydney, Sydney, New South Wales, Australia.
Adolescent male rodents and humans exhibit impairments in extinguishing learned fear. Here, we investigated whether female adolescent rats exhibit such impairments and if extinction is affected by the estrous cycle as in adults. Following fear conditioning to a discrete cue, female adolescent Sprague Dawley rats were extinguished either around the onset of puberty, when estrous cycling begins, or across different stages of the estrous cycle.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Behavioral Neuroscience Research Branch, Intramural Research Program, National Institute on Drug Abuse, Baltimore, MD 21224.
Learning when to initiate or withhold actions is essential for survival, requiring the integration of past experiences with new information to adapt to changing environments. The prelimbic cortex (PL) plays a central role in this process, with a stable PL neuronal population (ensemble) recruited during operant reward learning to encode response execution. However, it is unknown how this established reward-learning ensemble adapts to changing reward contingencies, such as reward omission during extinction.
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