Evidence map›Paper›PMID 17714770›Full record

ArticlePharmacology, biochemistry, and behavior2007

Agmatine reduces balance deficits in a rat model of third trimester binge-like ethanol exposure.

B Lewis, K A Wellmann, S Barron

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. A Rat Model of Fetal Alcohol Syndrome: A Series of Undergraduate Laboratory Exercises for Biopsychology Courses.Journal of undergraduate neuroscience education : JUNE : a publication of FUN, Faculty for Undergraduate Neuroscience · 2017
    Article
  5. Article
  6. Fetal alcohol spectrum disorders and neuroimmune changes.International review of neurobiology · 2014
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Focus on: neurotransmitter systems.Alcohol research & health : the journal of the National Institute on Alcohol Abuse and Alcoholism · 2011
    Review
  13. Fetal alcohol spectrum disorders: experimental treatments and strategies for intervention.Alcohol research & health : the journal of the National Institute on Alcohol Abuse and Alcoholism · 2011
    Review
  14. Fetal alcohol spectrum disorders: research challenges and opportunities.Alcohol research & health : the journal of the National Institute on Alcohol Abuse and Alcoholism · 2011
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

B LewisDepartment of Psychology, Kastle Hall, University of Kentucky, Lexington, KY 40506, USA.
K A Wellmann
S Barron
University of Kentucky · US

Funding

Polyamines in neonatal alcohol neurotoxicityR21AA014032 · NIAAA · UNIVERSITY OF KENTUCKY · PI BARRON, SUSAN · 2003 to 2005
$439k
NIAAA NIH HHS AA-014032NIAAA NIH HHS R21 AA014032
6 · The paper itself

Abstract

This study examined the effects of binge-like ethanol (ETOH) exposure in neonatal rats on a cerebellar-mediated balance task, and the ability of agmatine, an n-methyl-d-aspartate receptor (NMDAR) modulator, to reverse such effects. Five neonatal treatments groups were used, including ETOH (6.0 g/kg/day), AG (20 mg/kg), ETOH plus AG (6.0 g/kg/day and 20 mg/kg), a maltose control, and a non-treated control. Ethanol was administered via oral intubation twice daily for eight days, (AG was administered with the last ETOH intubation only). Two exposure periods were used; PND 1-8 or PND 8-15. On PND 31-33, balance performance on a single dowel was tested. Treatment with AG during withdrawal in ETOH exposed animals improved performance relative to ETOH alone among the PND 1-8 exposure period. ETOH exposure during the 2nd postnatal week did not impair balance. These findings provide further support that exposure to ETOH during critical developmental periods can impair performance on a cerebellar-dependent balance task. Of perhaps greater significance, co-administration of agmatine reduced these deficits suggesting that NMDA modulation via polyamine blockade may provide a novel approach to attenuating damage associated with binge-like ETOH consumption.

Indexed as

AgmatineAlcoholismAnimalsAnimals, NewbornArea Under CurveBody WeightCentral Nervous System DepressantsCerebellumDisease Models, AnimalEthanolFemaleFetal Alcohol Spectrum DisordersHumansMalePostural BalancePregnancyAgmatineCentral Nervous System DepressantsEthanolReceptors, N-Methyl-D-Aspartate

Identifiers

PMID17714770
PMCPMC2048752
OpenAlexW1966601233

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.