4.5 Review

Rodent models of early adversity: Impacts on developing social behavior circuitry and clinical implications

Journal

FRONTIERS IN BEHAVIORAL NEUROSCIENCE
Volume 16, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnbeh.2022.918862

Keywords

early life stress; dopamine; social behavior; habenula; reward

Funding

  1. NIH [BRAIN R00MH124434]
  2. Brain and Behavior Research Foundation

Ask authors/readers for more resources

Flexible and context-appropriate social functioning is crucial for survival, as it provides a template for future social processing. Early caregiving adversity can have lasting impacts on social behavior and increase vulnerability to psychiatric disorders. This article examines the neural circuit mechanisms underlying social behavior scaffolding, focusing on dopamine and its role in regions involved in social and threat processing. It also explores the relevance of altered dopamine signaling and dysfunction in social anhedonia among human populations with schizophrenia and major depressive disorder.
Flexible and context-appropriate social functioning is key for survival across species. This flexibility also renders social behavior highly plastic, particularly during early development when attachment to caregiver can provide a template for future social processing. As a result early caregiving adversity can have unique and lasting impacts on social behavior and even confer vulnerability to psychiatric disorders. However, the neural circuit mechanisms translating experience to outcome remain poorly understood. Here, we consider social behavior scaffolding through the lens of reward and threat processing. We begin by surveying several complementary rodent models of early adversity, which together have highlighted impacts on neural circuits processing social cues. We next explore these circuits underlying perturbed social functioning with focus on dopamine (DA) and its rote in regions implicated in social and threat processing such as the prefrontal cortex (PFC), basotateral amygdata (BLA) and the lateral habenula (LHb). Finally, we turn to human populations once more to examine how altered DA signaling and LHb dysfunction may play a role in social anhedonia, a common feature in diagnoses such as schizophrenia and major depressive disorder (MDD). We argue that this translational focus is critical for identifying specific features of adversity that confer heightened vulnerability for clinical outcomes involving social cue processing.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available