Evidence map›Paper›PMID 26446869›Full record

ArticlePsychopharmacology2015

Effects of NMDA receptor antagonists and antipsychotics on high frequency oscillations recorded in the nucleus accumbens of freely moving mice.

Mark J Hunt, Maciej Olszewski, Joanna Piasecka, Miles A Whittington, Stefan Kasicki

Open access · hybridAbstract read
In one paragraph

Article in Psychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. The M1/M4 preferring muscarinic agonist xanomeline modulates functional connectivity and NMDAR antagonist-induced changes in the mouse brain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
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  6. Review
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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 at 2 institutions in 2 countries.

Mark J HuntLaboratory of the Limbic System, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093, Warsaw, Poland. mhunt@nencki.gov.pl.
Maciej OlszewskiLaboratory of the Limbic System, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093, Warsaw, Poland.
Joanna PiaseckaLaboratory of the Limbic System, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093, Warsaw, Poland.
Miles A WhittingtonThe Hull York Medical School, University of York, Heslington, York, YO10 5DD, UK.
Stefan KasickiLaboratory of the Limbic System, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093, Warsaw, Poland.
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLUniversity of York · GB

Funding

Wellcome Trust 098352
6 · The paper itself

Abstract

rationaleAbnormal oscillatory activity associated with N-methyl-D-aspartate (NMDA) receptor hypofunction is widely considered to contribute to the symptoms of schizophrenia.

objectiveThis study aims to characterise the changes produced by NMDA receptor antagonists and antipsychotics on accumbal high-frequency oscillations (HFO; 130-180 Hz) in mice.

methodsLocal field potentials were recorded from the nucleus accumbens of freely moving mice.

resultsSystemic injection of ketamine and MK801 both dose-dependently increased the power of HFO and produced small increases in HFO frequency. The atypical antipsychotic drug, clozapine, produced a robust dose-dependent reduction in the frequency of MK801-enhanced HFO, whilst haloperidol, a typical antipsychotic drug, had little effect. Stimulation of NMDA receptors (directly or through the glycine site) as well as activation of 5-HT1A receptors, reduced the frequency of MK801-enhanced HFO, but other receptors known to be targets for clozapine, namely 5-HT2A, 5-HT7 and histamine H3 receptors had no effect.

conclusionsNMDA receptor antagonists and antipsychotics produce broadly similar fundamental effects on HFO, as reported previously for rats, but we did observe several notable differences. In mice, HFO at baseline were weak or not detectable unlike rats. Post-injection of NMDA receptor antagonists HFO was also weaker but significantly faster. Additionally, we found that atypical antipsychotic drugs may reduce the frequency of HFO by interacting with NMDA and/or 5-HT1A receptors.

Indexed as

AnimalsAntipsychotic AgentsClozapineDizocilpine MaleateDose-Response Relationship, DrugExcitatory Amino Acid AntagonistsHaloperidolKetamineMaleMiceNucleus AccumbensRats, WistarReceptors, N-Methyl-D-AspartateAntipsychotic AgentsClozapineDizocilpine MaleateExcitatory Amino Acid AntagonistsHaloperidolKetamineReceptors, N-Methyl-D-AspartateAntipsychoticsMiceNMDA receptor antagonistsOscillationsSchizophrenia

Identifiers

PMID26446869
PMCPMC4646921
OpenAlexW1956040624

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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.