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A Circuit Mechanism for Differentiating Positive and Negative Associations

The ability to differentiate stimuli predicting positive or negative outcomes is critical for survival, and perturbations of emotional processing underlie many psychiatric disease states. Synaptic plasticity in the basolateral amygdala complex (BLA) mediates the acquisition of associative memories,...

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Detalles Bibliográficos
Autores principales: Namburi, Praneeth, Beyeler, Anna, Yorozu, Suzuko, Calhoon, Gwendolyn G., Halbert, Sarah A., Wichmann, Romy, Holden, Stephanie S., Mertens, Kim L., Anahtar, Melodi, Felix-Ortiz, Ada C., Wickersham, Ian R., Gray, Jesse M., Tye, Kay M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418228/
https://www.ncbi.nlm.nih.gov/pubmed/25925480
http://dx.doi.org/10.1038/nature14366
Descripción
Sumario:The ability to differentiate stimuli predicting positive or negative outcomes is critical for survival, and perturbations of emotional processing underlie many psychiatric disease states. Synaptic plasticity in the basolateral amygdala complex (BLA) mediates the acquisition of associative memories, both positive(1,2) and negative(3–7). Different populations of BLA neurons may encode fearful or rewarding associations(8–10), but the identifying features of these populations and the synaptic mechanisms of differentiating positive and negative emotional valence have remained an enigma. Here, we show that BLA neurons projecting to the nucleus accumbens (NAc projectors) or the centromedial amygdala (CeM projectors) underwent opposing synaptic changes following fear or reward conditioning. We found that photostimulation of NAc projectors supports positive reinforcement while photostimulation of CeM projectors mediates negative reinforcement. Photoinhibition of CeM projectors impaired fear conditioning and enhanced reward conditioning. We then characterized these functionally-distinct neuronal populations by comparing their electrophysiological, morphological and genetic features. We provide a mechanistic explanation for the representation of positive and negative associations within the amygdala.