4.7 Article

Rewarded Extinction Increases Amygdalar Connectivity and Stabilizes Long-Term Memory Traces in the vmPFC

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JOURNAL OF NEUROSCIENCE
卷 42, 期 29, 页码 5717-5729

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SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0075-22.2022

关键词

amygdala; fear extinction; fMRI; reward; striatum; vmPFC

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Neurobiological evidence suggests that incorporating reward associations with an extinction memory may be an effective strategy to attenuate threat responses. This study compared rewarded extinction to standard extinction in both short-term and long-term retrieval tests and found that rewarded extinction was more effective in reducing arousal and threat expectancy. The study also identified different patterns of brain activity and connectivity between reward-associated extinction and standard extinction.
Neurobiological evidence in rodents indicates that threat extinction incorporates reward neurocircuitry. Consequently, incor-porating reward associations with an extinction memory may be an effective strategy to persistently attenuate threat responses. Moreover, while there is considerable research on the short-term effects of extinction strategies in humans, the long-term effects of extinction are rarely considered. In a within-subjects fMRI study with both female and male participants, we compared counterconditioning (CC; a form of rewarded-extinction) to standard extinction at recent (24 h) and remote (approximately one month) retrieval tests. Relative to standard extinction, rewarded extinction diminished 24-h relapse of arousal and threat expectancy, and reduced activity in brain regions associated with the appraisal and expression of threat (e.g., thalamus, insula, periaqueductal gray). The retrieval of reward-associated extinction memory was accompanied by func-tional connectivity between the amygdala and the ventral striatum, whereas the retrieval of standard-extinction memories was associated with connectivity between the amygdala and ventromedial prefrontal cortex (vmPFC). One month later, the re-trieval of both standard-extinction and rewarded-extinction was associated with amygdala-vmPFC connectivity. However, only rewarded extinction created a stable memory trace in the vmPFC, identified through overlapping multivariate patterns of fMRI activity from extinction to 24-h and one-month retrieval. These findings provide new evidence that reward may gener-ate a more stable and enduring memory trace of attenuated threat in humans.

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