Evidence map›Paper›PMID 29288725›Full record

ArticleNeuroscience letters2018

Both ketamine and NBQX attenuate alcohol drinking in male Wistar rats.

Jana Ruda-Kucerova, Zuzana Babinska, Matej Luptak, Bruk Getachew, Yousef Tizabi

Abstract read
In one paragraph

Article in Neuroscience letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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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.

Jana Ruda-KucerovaDepartment of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic. Electronic address: jkucer@med.muni.cz.
Zuzana BabinskaDepartment of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Matej LuptakDepartment of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Bruk GetachewDepartment of Pharmacology, Howard University College of Medicine, Washington, DC, USA.
Yousef TizabiDepartment of Pharmacology, Howard University College of Medicine, Washington, DC, USA.
Masaryk University · CZHoward University · US

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Novel Interventions in Alcohol Induced DepressionR03AA022479 · NIAAA · HOWARD UNIVERSITY · PI TIZABI, YOUSEF · 2014 to 2015
$149k
NIAAA NIH HHS R03 AA022479NICHD NIH HHS U54 HD090257
6 · The paper itself

Abstract

The devastating consequences of alcohol-use disorder (AUD) on the individual and the society are well established. Current treatments of AUD encompass various strategies, all of which have only modest effectiveness. Hence, there is a critical need to develop more efficacious therapies. Recently, specific glutamatergic receptors have been identified as potential novel targets for intervention in AUD. Thus, the current study was designed to evaluate the effects of acute administration of sub-anesthetic doses of ketamine, an NMDA receptor antagonist, as well as NBQX, an AMPA/kainate receptor antagonist on alcohol intake and its possible behavioural consequences. Adult male Wistar rats were trained in drinking in dark paradigm (3 weeks), and following stable alcohol intake, ketamine, NBQX as well as their combination were injected prior to a 90 min drinking session. In addition to alcohol intake, sucrose preference (overnight), and locomotor activity and forced swim test (FST) were also evaluated before and following alcohol intake. Both doses of ketamine (5 and 10 mg/kg) and NBQX (5 and 10 mg/kg) significantly attenuated percent alcohol intake. The combination of the higher dose of ketamine and NBQX, however, did not significantly affect percent alcohol intake. Moreover, animals exposed to alcohol showed decreased sucrose intake (reflective of anhedonia), decreased locomotor activity and swimming in the FST (reflective of helplessness), that were not affected by ketamine and/or NBQX. These results suggest that selective antagonism of the NMDA or AMPA/kainate receptors may be of therapeutic potential in AUD.

Indexed as

Alcohol DrinkingAnimalsDepressionKainic AcidKetamineMaleQuinoxalinesRats, WistarReceptors, AMPAReceptors, N-Methyl-D-Aspartate2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxalineKainic AcidKetamineQuinoxalinesReceptors, AMPAReceptors, N-Methyl-D-AspartateAlcoholismAlcohol use disorderAMPA receptorGlutamatergic receptorsKainate receptorNMDA receptor

Identifiers

PMID29288725
PMCPMC5805612
OpenAlexW2779559571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.