Evidence map›Paper›PMID 25420609›Full record

ArticlePsychopharmacology2015

Inhibition of alcohol self-administration by positive allosteric modulators of the GABAB receptor in rats: lack of tolerance and potentiation of baclofen.

Paola Maccioni, Daniela Vargiolu, Andrew W Thomas, Pari Malherbe, Claudia Mugnaini, Federico Corelli, Kimberly A Leite-Morris, Gian Luigi Gessa, Giancarlo Colombo

Abstract read
PubMed Publisher
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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 17% 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, 37 citations in OpenAlex.

  1. Article
  2. Novel medications for problematic alcohol use.The Journal of clinical investigation · 2024
    Review
  3. Delving into the reducing effects of the GABAAlcohol (Fayetteville, N.Y.) · 2023
    Article
  4. Review
  5. GABACurrent topics in behavioral neurosciences · 2022
    Article
  6. Article
  7. GABACurrent topics in behavioral neurosciences · 2022
    Review
  8. The GABAPsychopharmacology · 2021
    Article
  9. Review
  10. The Novel Positive Allosteric Modulator of the GABAFrontiers in cell and developmental biology · 2021
    Article
  11. Potential of GABACNS drugs · 2019
    Review
  12. Article
  13. Review
  14. Neural plasticity · 2017
    Review
  15. Article
  16. Article
  17. 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

9 authors at 5 institutions in 3 countries.

Paola MaccioniNeuroscience Institute, National Research Council of Italy, Section of Cagliari, S.S. 554, km. 4,500, 09042, Monserrato, CA, Italy.
Daniela Vargiolu
Andrew W Thomas
Pari Malherbe
Claudia Mugnaini
Federico Corelli
Kimberly A Leite-Morris
Gian Luigi Gessa
Giancarlo Colombo
National Research Council · ITRoche (Switzerland) · CHUniversity of Siena · ITBoston University · USNeuroscience Institute · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleTreatment with positive allosteric modulators (PAMs) of the GABAB receptor (GABAB PAMs) inhibits several alcohol-motivated behaviors in rodents, including operant, oral alcohol self-administration.

objectivesThe present study assessed the effects of (a) repeated administration of the GABAB PAMs, GS39783, and rac-BHFF and (b) a combination of an ineffective dose of either GS39783, or rac-BHFF, and an ineffective dose of the prototypic GABAB receptor agonist, baclofen, on operant, oral alcohol self-administration.

methodsStudies were conducted using selectively bred Sardinian alcohol-preferring (sP) rats exposed to a standard procedure of fixed ratio (FR) 4 (FR4) schedule of reinforcement for 15 % (v/v) alcohol.

resultsRepeated treatment with GS39783 (50 mg/kg, i.g.) or rac-BHFF (50 mg/kg, i.g.) produced an initial 40 % reduction in number of lever responses for alcohol and amount of self-administered alcohol that was maintained unaltered throughout the 10-day period of the GS39783 treatment and increased throughout the 5-day period of the rac-BHFF treatment. Combination of per se ineffective doses of GS39783 (5 mg/kg, i.g.), or rac-BHFF (5 mg/kg, i.g.), and baclofen (1 mg/kg, i.p.) reduced, by 35-45 %, both number of lever responses for alcohol and amount of self-administered alcohol.

conclusionsGS39783 and rac-BHFF (a) reduced alcohol reinforcing properties when given repeatedly, with no development of tolerance, and (b) potentiated baclofen effect. Both sets of data possess translational interest, as they suggest potential effectiveness of GABAB PAMs under chronic treatment and selective potentiation of baclofen effect.

Indexed as

Alcohol DrinkingAllosteric RegulationAnimalsBaclofenBenzofuransCyclopentanesDrug SynergismDrug ToleranceEthanolMalePyrimidinesRatsReceptors, GABA-BSelf AdministrationBaclofenBenzofuransCyclopentanesEthanolN,N'-dicyclopentyl-2-methylsulfanyl-5-nitro-pyrimidine-4,6-diaminePyrimidinesReceptors, GABA-B(R,S)-5,7-di-tert-butyl-3-hydroxy-3-trifluoromethyl-3H-benzofuran-2-one

Identifiers

PMID25420609
OpenAlexW2052777660

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.