Evidence map›Paper›PMID 17046721›Full record

ArticleBiological psychiatry2007

Fine-tuning of awake prefrontal cortex neurons by clozapine: comparison with haloperidol and N-desmethylclozapine.

Houman Homayoun, Bita Moghaddam

Open access · greenAbstract readComparative Study
In one paragraph

Article in Biological psychiatry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 19% of its field
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

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Effects of Ketamine on Frontoparietal Interactions in a Rule-Based Antisaccade Task in Macaque Monkeys.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. From revolution to evolution: the glutamate hypothesis of schizophrenia and its implication for treatment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Orbitofrontal cortex neurons as a common target for classic and glutamatergic antipsychotic drugs.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  17. Extended access to cocaine self-administration produces long-lasting prefrontal cortex-dependent working memory impairments.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2008
    Article
  18. Divergent plasticity of prefrontal cortex networks.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2008
    Review
  19. NMDA receptor hypofunction produces opposite effects on prefrontal cortex interneurons and pyramidal neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    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

2 authors at 1 institution in 1 country.

Houman HomayounDepartment of Neurosciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Bita Moghaddam
University of Pittsburgh · US

Funding

Neurochemical Effects of Antipsychotic DrugsR37MH048404 · NIMH · YALE UNIVERSITY · PI MOGHADDAM, BITA · 2002 to 2012
$3.4M
NIMH NIH HHS R37 MH048404
6 · The paper itself

Abstract

backgroundMechanisms underlying clozapine's better clinical efficacy in schizophrenia remain poorly understood. The prefrontal cortex (PFC) has been implicated as a primary site for the therapeutic effects of clozapine; however, evidence for how clozapine influences the activity of PFC neurons in behaviorally relevant contexts is lacking.

methodsEnsemble single unit recording in awake rats was used to measure the activity of PFC neurons in response to clozapine, its main metabolite N-desmethylclozapine (DMClz), and the typical antipsychotic drug haloperidol during baseline conditions and after treatment with the N-methyl-D-aspartate antagonist MK801. Behavioral stereotypy was scored during recording.

resultsClozapine and DMClz but not haloperidol had an activity-dependent influence on spontaneous firing rate of PFC cells: they increased the activity of neurons with low baseline firing rates and decreased the activity of neurons with higher firing rates. Clozapine and DMClz but not haloperidol also reversed the effect of MK801 on PFC neuronal firing. This reversal was strongly correlated with blockade of MK801-induced behavioral stereotypy.

conclusionsThese findings indicate that clozapine has the capacity to fine-tune spontaneous and disrupted activity of PFC neurons. This effect might contribute, in part, to the therapeutic efficacy of clozapine in schizophrenia.

Indexed as

Action PotentialsAnalysis of VarianceAnimalsAntipsychotic AgentsClozapineDizocilpine MaleateDose-Response Relationship, DrugDrug InteractionsExcitatory Amino Acid AntagonistsHaloperidolMaleNeuronsPrefrontal CortexRatsRats, Sprague-DawleyStereotyped BehaviorAntipsychotic AgentsClozapineDizocilpine MaleateExcitatory Amino Acid AntagonistsHaloperidolnorclozapine

Identifiers

PMID17046721
PMCPMC2910426
OpenAlexW2071790368

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.