4.7 Article

Changes in Appetitive Associative Strength Modulates Nucleus Accumbens, But Not Orbitofrontal Cortex Neuronal Ensemble Excitability

期刊

JOURNAL OF NEUROSCIENCE
卷 37, 期 12, 页码 3160-3170

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3766-16.2017

关键词

appetitive learning; Fos; intrinsic excitability; neuronal ensemble; nucleus accumbens; prefrontal cortex

资金

  1. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/M009017/1]
  2. University of Sussex Strategic Development Funds
  3. Sussex Neuroscience
  4. Sussex School of Psychology Impact Funds
  5. BBSRC [BB/M009017/1] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BB/M009017/1] Funding Source: researchfish

向作者/读者索取更多资源

Cues that predict the availability of food rewards influence motivational states and elicit food-seeking behaviors. If a cue no longer predicts food availability, then animals may adapt accordingly by inhibiting food-seeking responses. Sparsely activated sets of neurons, coined neuronal ensembles,have been shown to encode the strength of reward-cue associations. Although alterations in intrinsic excitability have been shown to underlie many learning and memory processes, little is known about these properties specifically on cue-activated neuronal ensembles. We examined the activation patterns of cue-activated orbitofrontal cortex(OFC) and nucleus accumbens(NAc) shell ensembles using wild-typeand Fos-GFP mice, which express green fluorescent protein (GFP) in activated neurons, after appetitive conditioning with sucrose and extinction learning. We also investigated the neuronal excitability of recently activated, GFP + neurons in these brain areas using whole-cell electrophysiology in brain slices. Exposure to a sucrose cue elicited activation of neurons in both the NAc shell and OFC. In the NAc shell, but not the OFC, these activated GFP + neurons were more excitable than surrounding GFP-neurons. After extinction, the number of neurons activated in both areas was reduced and activated ensembles in neither area exhibited altered excitability. These data suggest that learning-induced alterations in the intrinsic excitability of neuronal ensembles is regulated dynamically across different brain areas. Furthermore, we show that changes in associative strength modulate the excitability profile of activated ensembles in the NAc shell.

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