Evidence map›Paper›PMID 24776303›Full record

ArticleAlcohol (Fayetteville, N.Y.)2014

New evidence of ethanol's anxiolytic properties in the infant rat.

Roberto Sebastián Miranda-Morales, Michael E Nizhnikov, Dustin H Waters, Norman E Spear

Abstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  5. Review
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

4 authors at 1 institution in 1 country.

Roberto Sebastián Miranda-MoralesDepartment of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY 13902-6000, USA. Electronic address: smiranda@immf.uncor.edu.
Michael E NizhnikovDepartment of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY 13902-6000, USA.
Dustin H WatersDepartment of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY 13902-6000, USA.
Norman E SpearDepartment of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY 13902-6000, USA.
Binghamton University · US

Funding

Social Anxiety, Stress and Ethanol Sensitivity in Adolescence and AdulthoodP50AA017823 · NIAAA · UPSTATE MEDICAL UNIVERSITY · PI Marvin Rafael Diaz · 2009 to 2026
$30.5M
Ethanol Intake and Reinforcement in Infant RatsR01AA013098 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI SPEAR, NORMAN E · 2002 to 2012
$2.8M
EARLY ETHANOL--ANALYSIS AND PERSISTENCE OF CONSEQUENCESR01AA011960 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI SPEAR, NORMAN E · 1998 to 2008
$1.8M
Ontogeny of Response to Ethanol After Prenatal EthanolR01AA015992 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI SPEAR, NORMAN E · 2006 to 2010
$1.6M
NIAAA NIH HHS AA013098NIAAA NIH HHS AA015992NIAAA NIH HHS AA11960NIAAA NIH HHS P50 AA017823NIAAA NIH HHS P50AA017823NIAAA NIH HHS R01 AA011960NIAAA NIH HHS R01 AA013098NIAAA NIH HHS R01 AA015992
6 · The paper itself

Abstract

Ethanol induces appetitive, aversive, and anxiolytic effects that are involved in the development of ethanol use and dependence. Because early ethanol exposure produces later increased responsiveness to ethanol, considerable effort has been devoted to analysis of ethanol's appetitive and aversive properties during early ontogeny. Yet, there is a relative scarcity of research related to the anxiolytic effects of ethanol during early infancy, perhaps explained by a lack of age-appropriate tests. The main aim of this study was to validate a model for the assessment of ethanol's anxiolytic effects in the infant rat (postnatal days 13-16). The potentially anxiolytic effects of ethanol tested included: i) amelioration of conditioned place aversion, ii) ethanol intake in the presence of an aversive conditioned stimulus, iii) the inhibitory behavioral effect in an anxiogenic environment, and iv) innate aversion to a brightly illuminated area in a modified light/dark paradigm. Ethanol doses employed across experiments were 0.0, 0.5, and 2.0 g/kg. Results indicated that a low ethanol dose (0.5 g/kg) was effective in attenuating expression of a conditioned aversion. Ethanol intake, however, was unaffected by simultaneous exposure to an aversive stimulus. An anxiogenic environment diminished ethanol-induced locomotor stimulation. Finally, animals given 0.5 g/kg ethanol and evaluated in a light/dark box showed increased time spent in the illuminated area and increased latency to escape from the brightly lit compartment than rats treated with a higher dose of ethanol or vehicle. These new results suggest that ethanol doses as low as 0.5 g/kg are effective in ameliorating an aversive and/or anxiogenic state in preweanling rats. These behavioral preparations can be used to assess ethanol's anxiolytic properties during early development.

Indexed as

Alcohol DrinkingAgingAnimalsAnti-Anxiety AgentsConditioning, PsychologicalEthanolExploratory BehaviorMotor ActivityPyrrolidinesRats, Sprague-DawleyAnti-Anxiety AgentsEthanolPyrrolidinesspiradolineAnxiolysisConditioned aversionEthanol motivational propertiesInfant ratLight/dark test

Identifiers

PMID24776303
PMCPMC4035812
OpenAlexW2064832506

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.