It is demonstrated that AIC excitatory neurons, specifically layer 5 pyramidal neurons projecting to the basolateral amygdala, are essential for higher-order threat learning/memory and a novel circuit mechanism for bidirectional regulation of higher-order threat learning/memory is identified.
Abstract
Learning about potential threats is indispensable for survival, and its deficits underlie numerous neuropsychiatric disorders. Human brain imaging suggests the anterior insular cortex (AIC) as a key neural correlate of threat learning, yet its mechanistic role remains unclear. Leveraging multimodal systems neuroscience approaches, we demonstrate that AIC excitatory neurons, specifically layer 5 pyramidal neurons projecting to the basolateral amygdala, are essential for higher-order threat learning/memory. They are specifically required when a predictor is temporally separated from an aversive event or when the predictive information is embedded within a diffuse context. In contrast, the AIC is dispensable for elementary, temporally contiguous threat learning. Surprisingly, while the AIC promotes memory formation, it also constrains the level of fear expression during retrieval in a context-dependent manner. This bidirectional control is mediated by the recruitment of distinct AIC neuronal ensembles. Together, we identify a novel circuit mechanism for bidirectional regulation of higher-order threat learning/memory.
A virtual reality paradigm is used to disentangle spatial, temporal, and emotional memory features in the mouse ventral CA1 hippocampus and shows that distinct spatial and temporal representations emerge for context- and cue-related features, with temporal features transferring to novel experiences.
Anastasija Milentijevic, Carlo Cerquetella, Thomas Nevian et al.· Current Biology· 0 citations
Abstract Background Environmental cues present during threatening situations become linked to danger. When these cues are encountered again, they trigger retrieval of a fear memory via specialized neural circuits that produce internal fear states and initiate defensive behaviors. In brain areas such as the basolateral...
A. Holmes· International Journal of Neu...· 0 citations
A timely and comprehensive view of the anterior cingulate cortex’s role in adaptive and pathological anxiety is provided and an integrative model in which ACC effects depend on subregion, projection target, and behavioral context is proposed.
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Flexible behavior depends on neural mechanisms that integrate memory with ongoing motivational demands. Studies have revealed dopamine (DA) to have an essential role in mediating memory, behavioral flexibility, and decision-making, yet the dopaminergic contributions within prefrontal-hippocampal circuits remain poorly...
Albit Caban-Murillo, Michelle Surets, Celine Chien et al.· Current Biology· 0 citations
Flexible behavior depends on continuous updating of internal models, yet the neural circuits coordinating this process remain poorly understood. The claustrum, which is reciprocally connected to nearly the entire neocortex, is uniquely positioned to influence cortical processing. Here we report single-neuron recordings...
The brain’s ability to consolidate a wide range of memories while maintaining their distinctiveness across experiences remains poorly understood. Sharp-wave ripples, neural oscillations that occur predominantly within CA1 of the hippocampus during immobility and sleep, have been shown to play a critical role in the con...
Arron F. Hall, Dong V. Wang· bioRxiv· 2 citations
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