Evidence map›Paper›PMID 26985040›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Anxiety Evokes Hypofrontality and Disrupts Rule-Relevant Encoding by Dorsomedial Prefrontal Cortex Neurons.

Junchol Park, Jesse Wood, Corina Bondi, Alberto Del Arco, Bita Moghaddam

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Acute psilocybin enhances cognitive flexibility in rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  10. Article
  11. Acute psilocybin enhances cognitive flexibility in rats.bioRxiv : the preprint server for biology · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Junchol ParkDepartments of Neuroscience and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.
Jesse WoodDepartments of Neuroscience and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.
Corina BondiDepartments of Neuroscience and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.
Alberto Del ArcoDepartments of Neuroscience and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.
Bita MoghaddamDepartments of Neuroscience and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260 bita@pitt.edu.

Funding

Training for Transformative Discovery in PsychiatryT32MH016804 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SWEET, ROBERT A · 1985 to 2025
$6.2M
NEUROCHEMICAL EFFECTS OF ANTIPSYCHOTIC DRUGSR01MH048404 · NIMH · YALE UNIVERSITY · PI BITA MOGHADDAM · 1997 to 2026
$5.0M
Neurochemical Effects of Antipsychotic DrugsR37MH048404 · NIMH · YALE UNIVERSITY · PI MOGHADDAM, BITA · 2002 to 2012
$3.4M
Inhibitory Control of Prefrontal CortexR01MH084906 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MOGHADDAM, BITA · 2009 to 2013
$1.8M
Inhibitory Control of Prefrontal CortexR56MH084906 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI MOGHADDAM, BITA · 2017 to 2017
$491k
NEUROCHEMICAL EFFECTS OF ANTIPSYCHOTIC DRUGSR29MH048404 · NIMH · YALE UNIVERSITY · PI MOGHADDAM, BITA · 1992 to 1996
–
NIMH NIH HHS MH048404NIMH NIH HHS MH084906NIMH NIH HHS R01 MH048404NIMH NIH HHS R01 MH084906NIMH NIH HHS R37 MH048404NIMH NIH HHS R56 MH084906NIMH NIH HHS T32 MH016804
6 · The paper itself

Abstract

Anxiety is a debilitating symptom of most psychiatric disorders, including major depression, post-traumatic stress disorder, schizophrenia, and addiction. A detrimental aspect of anxiety is disruption of prefrontal cortex (PFC)-mediated executive functions, such as flexible decision making. Here we sought to understand how anxiety modulates PFC neuronal encoding of flexible shifting between behavioral strategies. We used a clinically substantiated anxiogenic treatment to induce sustained anxiety in rats and recorded from dorsomedial PFC (dmPFC) and orbitofrontal cortex (OFC) neurons while they were freely moving in a home cage and while they performed a PFC-dependent task that required flexible switches between rules in two distinct perceptual dimensions. Anxiety elicited a sustained background "hypofrontality" in dmPFC and OFC by reducing the firing rate of spontaneously active neuronal subpopulations. During task performance, the impact of anxiety was subtle, but, consistent with human data, behavior was selectively impaired when previously correct conditions were presented as conflicting choices. This impairment was associated with reduced recruitment of dmPFC neurons that selectively represented task rules at the time of action. OFC rule representation was not affected by anxiety. These data indicate that a neural substrate of the decision-making deficits in anxiety is diminished dmPFC neuronal encoding of task rules during conflict-related actions. Given the translational relevance of the model used here, the data provide a neuronal encoding mechanism for how anxiety biases decision making when the choice involves overcoming a conflict. They also demonstrate that PFC encoding of actions, as opposed to cues or outcome, is especially vulnerable to anxiety. SIGNIFICANCE STATEMENT: A debilitating aspect of anxiety is its impact on decision making and flexible control of behavior. These cognitive constructs depend on proper functioning of the prefrontal cortex (PFC). Understanding how anxiety affects PFC encoding of cognitive events is of great clinical and evolutionary significance. Using a clinically valid experimental model, we find that, under anxiety, decision making may be skewed by salient and conflicting environmental stimuli at the expense of flexible top-down guided choices. We also find that anxiety suppresses spontaneous activity of PFC neurons, and weakens encoding of task rules by dorsomedial PFC neurons. These data provide a neuronal encoding scheme for how anxiety disengages PFC during decision making.

Indexed as

Action PotentialsAnimalsAnxietyAttentionCarbolinesDisease Models, AnimalGABA AntagonistsLinear ModelsMaleMaze LearningNeuronsPrefrontal CortexRatsRats, Sprague-DawleyROC CurveWakefulnessCarbolinesFG 7142GABA Antagonistsaddictiondecision makingdopamineschizophreniastress

Identifiers

PMID26985040
PMCPMC4792942

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.