Journal
NATURE NEUROSCIENCE
Volume 24, Issue 4, Pages 516-528Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41593-020-00784-3
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Funding
- US National Institutes of Health [EY019049, MH116990, R01DC008983, RF1MH114112]
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Research has found that anxiogenic stressors can elicit acute and prolonged responses in glutamatergic neurons of the mouse medial preoptic area, affecting the induction and expression of anxiety-like behaviors and the production of anxiolytic effects. These neurons interact to play important roles in coordinating emotional state and social behavior.
Anxiety is a negative emotional state that is overly displayed in anxiety disorders and depression. Although anxiety is known to be controlled by distributed brain networks, key components for its initiation, maintenance and coordination with behavioral state remain poorly understood. Here, we report that anxiogenic stressors elicit acute and prolonged responses in glutamatergic neurons of the mouse medial preoptic area (mPOA). These neurons encode extremely negative valence and mediate the induction and expression of anxiety-like behaviors. Conversely, mPOA GABA-containing neurons encode positive valence and produce anxiolytic effects. Such opposing roles are mediated by competing local interactions and long-range projections of neurons to the periaqueductal gray. The two neuronal populations antagonistically regulate anxiety-like and parental behaviors: anxiety is reduced, while parenting is enhanced and vice versa. Thus, by evaluating negative and positive valences through distinct but interacting circuits, the mPOA coordinates emotional state and social behavior.
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