Changes in Appetitive Associative Strength Modulates Nucleus Accumbens, But Not Orbitofrontal Cortex Neuronal
Joseph J Ziminski1, Sabine Hessler1, Gabriella Margetts-Smith1
1Sussex Neuroscience, School of Psychology, University of Sussex, Falmer BN1 9QG, United Kingdom.
Summary
Neuronal ensembles in the nucleus accumbens become more excitable after learning food cues, but this changes with extinction. This highlights dynamic regulation of brain excitability in reward learning.
Area of Science:
- Neuroscience
- Behavioral Neuroscience
- Cellular Electrophysiology
Background:
- Learned associations between cues and food rewards drive motivated behaviors.
- Neuronal ensembles are thought to encode these associations.
- Changes in neuronal excitability are implicated in learning, but specific changes in cue-activated ensembles are unclear.
Purpose of the Study:
- To investigate alterations in neuronal excitability within cue-activated ensembles in the orbitofrontal cortex (OFC) and nucleus accumbens (NAc) shell.
- To determine if these excitability changes are dynamic and adapt to associative learning and extinction.
Main Methods:
- Used Fos-GFP mice to identify cue-activated neuronal ensembles in the OFC and NAc shell after appetitive conditioning and extinction.
- Employed whole-cell electrophysiology to measure the intrinsic excitability of GFP+ neurons within these ensembles.
Main Results:
- Sucrose cue exposure activated neuronal ensembles in both the NAc shell and OFC.
- Activated neurons in the NAc shell, but not OFC, showed increased excitability compared to non-activated neurons.
- Following extinction learning, ensemble activation decreased, and altered excitability was no longer observed in either brain area.
Conclusions:
- Learning-induced changes in neuronal ensemble excitability are regulated dynamically and differ across brain regions.
- The nucleus accumbens shell, but not the OFC, exhibits altered neuronal excitability in activated ensembles, which is modulated by associative strength.
- These findings reveal differential regulation and dynamic adaptation of intrinsic excitability in brain areas encoding appetitive memories.
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