Published November 12, 2024 | Version v1

Valence and salience encoding in the central amygdala

  • 1. University of Washington

Description

The central amygdala (CeA) has emerged as an important brain region for regulating both negative (fear and anxiety) and positive (reward) affective behaviors. The CeA has been proposed to encode affective information in the form of valence (whether the stimulus is good or bad) or salience (how significant is the stimulus), but the extent to which these two types of stimulus representation occur in the CeA is not known. Here, we used single cell calcium imaging in mice during appetitive and aversive conditioning and found that majority of CeA neurons (~65%) encode the valence of the unconditioned stimulus (US) with a smaller subset of cells (~15%) encoding the salience of the US. Valence and salience encoding of the conditioned stimulus (CS) was also observed, albeit to a lesser extent. These findings show that the CeA is a site of convergence for encoding oppositely valenced US information.

Notes

Funding provided by: National Institute of Mental Health
ROR ID: https://ror.org/04xeg9z08
Award Number: F32MH127801

Funding provided by: National Institute of Mental Health
ROR ID: https://ror.org/04t0s7x83
Award Number: R01MH104450

Funding provided by: National Institute on Drug Abuse
ROR ID: https://ror.org/00fq5cm18
Award Number: P30DA048736

Methods

The 1-photon calcium imaging data were pre-processed and motion-corrected using the Inscopix Data Processing Software (IDPS). Cell identification was performed with a constrained non-negative matrix factorization algorithm for microendoscopic data (CNMF-E) within IDPS. All cell traces were then statistically tested using the 'circular shifting' method to determine whether their responses were significant. The code for the circular shifting method is available at https://github.com/zweifellab?tab=repositories. ++ Additionally, circular shift analysis tools (R base) have been uploaded in this dataset. 

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Additional details

Related works

Is cited by
10.1101/2024.07.05.602310 (DOI)
Is source of
10.5061/dryad.zgmsbccng (DOI)