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Key Brain Circuitry for Social Valence Offers Hope for Autism Therapies

Mount Sinai researchers identify opposing roles of serotonin and neurotensin in the hippocampus, paving the way for targeted treatments for social deficits in autism spectrum disorder.

While deficits in social valence are known to be prevalent in many neuropsychiatric disorders, their underlying neural mechanisms and pathophysiology have remained elusive. Credit: Neuroscience News
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Overview

  • Scientists mapped the ventral CA1 hippocampal circuitry, revealing how serotonin and neurotensin encode opposing emotional values for social interactions.
  • Serotonin acting on the 1B receptor generates positive impressions, while neurotensin acting on the 1 receptor creates negative impressions of social encounters.
  • A novel behavioral paradigm exposed mice to positive (potential mate) and negative (aggressive conspecific) interactions to study learned social preferences.
  • Activating the serotonin 1B receptor in a mouse model of autism spectrum disorder restored positive social impressions, addressing key social deficits.
  • This discovery highlights potential therapeutic targets for neuropsychiatric disorders such as autism and schizophrenia, with implications for improving social cognition.