Evidence map›Paper›PMID 21487655›Full record

ArticlePsychopharmacology2011

Ethanol concentration-dependent effects and the role of stress on ethanol drinking in corticotropin-releasing factor type 1 and double type 1 and 2 receptor knockout mice.

Raúl Pastor, Cheryl Reed, Sue Burkhart-Kasch, Na Li, Amanda L Sharpe, Sarah C Coste, Mary P Stenzel-Poore, Tamara J Phillips

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. The Role of the Central Amygdala in Alcohol Dependence.Cold Spring Harbor perspectives in medicine · 2021
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Corticotropin-Releasing Factor (CRF) and Addictive Behaviors.International review of neurobiology · 2017
    Review
  11. Review
  12. Genes and Alcohol Consumption: Studies with Mutant Mice.International review of neurobiology · 2016
    Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Role of corticotropin-releasing factor and corticosterone in behavioral sensitization to ethanol.The Journal of pharmacology and experimental therapeutics · 2012
    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

8 authors at 1 institution in 1 country.

Raúl PastorBehavioral Neuroscience Department and Portland Alcohol Research Center, Oregon Health & Science University, Portland, OR, USA.
Cheryl Reed
Sue Burkhart-Kasch
Na Li
Amanda L Sharpe
Sarah C Coste
Mary P Stenzel-Poore
Tamara J Phillips
Oregon Health & Science University · US

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Suzanne S. Fei · 2006 to 2026
$34.5M
CRH Receptors and Stress Response PathwaysR01MH065689 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI STENZEL-POORE, MARY P · 2003 to 2007
$1.8M
Studies of CRH and Alcohol EffectsR01AA013331 · NIAAA · OREGON HEALTH AND SCIENCE UNIVERSITY · PI PHILLIPS, TAMARA J. · 2001 to 2005
$1.7M
NIAAA NIH HHS P60 AA010760NIAAA NIH HHS P60AA010760NIAAA NIH HHS R01 AA013331NIAAA NIH HHS R01AA13331NIMH NIH HHS R01 MH065689NIMH NIH HHS R01MH65689
6 · The paper itself

Abstract

rationaleExposure to stressors promotes ethanol (EtOH) consumption and enhances drug craving during abstinence. Corticotropin-releasing factor (CRF), and in particular, CRF actions via type 1 CRF receptors (CRF(1)) are critical in behavioral responses to stressors. CRF(1) play a role in EtOH-induced behavioral neuroadaptation, in binge-like EtOH consumption, and in heightened EtOH consumption in dependent animals.

objectivesWe investigated the involvement of CRF(1) in swim-stress-induced changes in EtOH consumption and in baseline consumption as a function of EtOH concentration. The role of CRF(2) in adapting to effects of the stressor was also examined.

methodsWild-type mice and knockout mice lacking CRF(1) were tested for two-bottle choice EtOH consumption at concentrations of 3-20%. Also, intake of 10% EtOH was examined in wild-type mice and knockout mice lacking CRF(1), or lacking both CRF(1) and CRF(2), before and after acute or repeated swim stress exposures.

resultsEtOH intake was reduced in CRF(1) compared with wild-type mice when presented at a concentration of 20% but not when presented at lower concentrations. No genotype-dependent effects were found for saccharin or quinine drinking. Acute swim stress had no effect, but repeated swim stress resulted in higher levels of EtOH consumption in wild-type mice, compared with both types of knockout mice. Stress effects on EtOH drinking were longer lasting in double knockout mice.

conclusionsThese data suggest a prominent role of CRF(1) in stressor-induced changes in EtOH consumption, with involvement of CRF(2) in recovery from stressor effects.

Indexed as

Alcohol DrinkingAnimalsCRF Receptor, Type 1Disease Models, AnimalDose-Response Relationship, DrugEthanolFemaleGenotypeMaleMiceMice, Inbred C57BLMice, KnockoutQuinineReceptors, Corticotropin-Releasing HormoneSaccharinStress, PsychologicalCRF Receptor, Type 1CRF receptor type 2EthanolQuinineReceptors, Corticotropin-Releasing HormoneSaccharin

Identifiers

PMID21487655
PMCPMC3312392
OpenAlexW2082762685

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.