Evidence map›Paper›PMID 23474845›Full record

ArticlePsychopharmacology2013

The antipsychotic-like effects of the mGlu group III orthosteric agonist, LSP1-2111, involves 5-HT₁A signalling.

Joanna M Wierońska, Francine C Acher, Anna Sławińska, Piotr Gruca, Magdalena Lasoń-Tyburkiewicz, Mariusz Papp, Andrzej Pilc

Open access · hybridAbstract read
In one paragraph

Article in Psychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Effect of the mGluPsychopharmacology · 2023
    Article
  4. New 1,2,4-oxadiazole derivatives with positive mGluJournal of enzyme inhibition and medicinal chemistry · 2022
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. The functional cooperation of 5-HTPharmacological reports : PR · 2020
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

7 authors at 4 institutions in 2 countries.

Joanna M WierońskaInstitute of Pharmacology, Polish Academy of Sciences, 31-343 Kraków, Poland. wierons@if-pan.krakow.pl
Francine C Acher
Anna Sławińska
Piotr Gruca
Magdalena Lasoń-Tyburkiewicz
Mariusz Papp
Andrzej Pilc
Maj Institute of Pharmacology · PLInstitute of Nuclear Physics, Polish Academy of Sciences · PLPolish Academy of Sciences · PLUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleSeveral studies have suggested that modulation of the glutamatergic system via metabotropic glutamate receptors (mGlu) could be a new way to achieve antipsychotic-like activity. LSP1-2111, the group III mGlu receptor orthosteric agonist, with a high affinity towards mGlu4 receptors, was previously shown to exhibit antipsychotic-like action in animal models displaying positive symptoms of schizophrenia.

objectivesHere, we decided to investigate the possible role of LSP1-2111 in models of negative (social interaction) and cognitive (NOR) symptoms of psychosis. We also investigated the involvement of 5-HT1A receptors in the LSP1-2111-induced antipsychotic effects. Apart from the above-mentioned models of negative and cognitive symptoms, MK-801 and amphetamine-induced hyperactivity tests, plus the DOI-induced head twitches in mice as models for positive symptoms of psychosis, were used in this part of the investigations.

resultsLSP1-2111 (0.5, 2, and 5 mg/ kg) dose-dependently inhibited MK-801-induced deficits in social interaction and NOR tests. The effects of the drug were antagonized by 5-HT1A antagonist, WAY100635 (0.1 mg/kg). A similar inhibition of LSP1-2111-induced effects was observed in models of positive symptoms of schizophrenia. Moreover, the concomitant administration of subeffective doses of LSP1-2111 (0.3-0.5 mg/kg) with a subeffective dose of 5-HT1A agonist, (R)-(+)-8-Hydroxy-DPAT (0.01 mg/kg), induced a clear antipsychotic-like effect in all of the procedures used.

conclusionsAltogether, we propose that the activation of group III mGlu receptors may be a promising target for the development of novel antipsychotic drugs, towards not only positive but also negative and cognitive symptoms. The action of the compound is 5-HT1A-dependent.

Indexed as

8-Hydroxy-2-(di-n-propylamino)tetralinAminobutyratesAmphetaminesAnimalsAntipsychotic AgentsCyclohexanesDextroamphetamineDisease Models, AnimalDizocilpine MaleateDose-Response Relationship, DrugMaleMicePhosphinic AcidsPiperazinesPsychotic DisordersRats4-iodo-2,5-dimethoxyphenylisopropylamine8-Hydroxy-2-(di-n-propylamino)tetralinAminobutyratesAmphetaminesAntipsychotic AgentsCyclohexanesDextroamphetamineDizocilpine MaleateLSP1 2111metabotropic glutamate receptor 4Phosphinic AcidsPiperazinesReceptor, Serotonin, 5-HT1AReceptors, Metabotropic GlutamateWAY 101363

Identifiers

PMID23474845
PMCPMC3663209
OpenAlexW2061349972

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Registered trials

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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.