4.7 Article

Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex

期刊

JOURNAL OF NEUROSCIENCE
卷 39, 期 23, 页码 4595-4605

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2031-18.2019

关键词

Fragile X syndrome; habit; orbital; prefrontal; response-outcome; stimulus-response

资金

  1. Children's Healthcare of Atlanta
  2. NIH [MH101477, MH117103, MH103748, GM008602, GM000680]
  3. Office of Research Infrastructure Programs [OD P51OD011132]
  4. NINDS Core Facilities Grant [P30NS055077]
  5. Emory Egleston Children's Research Center

向作者/读者索取更多资源

An essential aspect of goal-directed decision-making is selecting actions based on anticipated consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plasticity of dendritic spines in this region. To investigate this possibility, we trained male and female mice to nose poke for food reinforcers, or we delivered the same number of food reinforcers non-contingently to separate mice. We then decreased the likelihood of reinforcement for trained mice, requiring them to modify action-outcome expectations. In a separate experiment, we blocked action-outcome updating via chemogenetic inactivation of the OFC. In both cases, successfully selecting actions based on their likely consequences was associated with fewer immature, thin-shaped dendritic spines and a greater proportion of mature, mushroom-shaped spines in the ventrolateral OFC. This pattern was distinct from spine loss associated with aging, and we identified no effects on hippocampal CA1 neurons. Given that the OFC is involved in prospective calculations of likely outcomes, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for solidifying durable expectations. To investigate causal relationships, we inhibited the RNA-binding protein fragile X mental retardation protein (encoded by Fmr1), which constrains dendritic spine turnover. Ventrolateral OFC-selective Fmr1 knockdown recapitulated the behavioral effects of inducible OFC inactivation (and lesions; also shown here), impairing action-outcome conditioning, and caused dendritic spine excess. Our findings suggest that a proper balance of dendritic spine plasticity within the OFC is necessary for one's ability to select actions based on anticipated consequences.

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