Evidence map›Paper›PMID 27687801›Full record

ArticleNeuroscience2016

Exposure to alcohol during adolescence exerts long-term effects on stress response and the adult brain stress circuits.

Camryn D Allen, Jan-Sebastian Grigoleit, Joonho Hong, Sejin Bae, Joan Vaughan, Soon Lee

Abstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Longitudinal associations between binge drinking and changes in behavioral and neural threat reactivity in youth.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Adolescent neuroimmune function and its interaction with alcohol.International review of neurobiology · 2022
    Review
  8. Article
  9. Article
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  11. Article
  12. Review
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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

6 authors at 1 institution in 1 country.

Camryn D AllenThe Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, La Jolla, CA 92037, USA.
Jan-Sebastian GrigoleitLaboratory of Neuronal Structure and Function, The Salk Institute, La Jolla, CA 92037, USA.
Joonho HongThe Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, La Jolla, CA 92037, USA.
Sejin BaeThe Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, La Jolla, CA 92037, USA.
Joan VaughanThe Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, La Jolla, CA 92037, USA.
Soon LeeThe Clayton Foundation Laboratories for Peptide Biology, The Salk Institute, La Jolla, CA 92037, USA. Electronic address: slee@salk.edu.
Salk Institute for Biological Studies · US

Funding

Adolescent alcohol exposure and altered adult HPA axis activityU01AA019973 · NIAAA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, SOON O · 2010 to 2014
$2.1M
NIAAA NIH HHS U01 AA019973
6 · The paper itself

Abstract

The hypothalamic-pituitary-adrenal (HPA) axis undergoes critical developments during adolescence. Therefore, stressors experienced during this period potentially have long-term effects on adult HPA axis function. We hypothesized that adolescent intermittent ethanol (AIE) exposure would affect adult HPA axis function, resulting in altered responses to an alcohol challenge in young adults or adults. To test these hypotheses, male rats were exposed to alcohol vapor for 6h per day from post-natal day (PND) 28-42, then acutely challenged with alcohol intragastrically (3.2-4.5g/kg) in young adults (PND 70) or adults (PND 90). Overall, we observed blunted HPA axis responses to an alcohol challenge due to AIE exposure. Specifically, AIE tended to inhibit the alcohol challenge-induced increase in plasma corticosterone (CORT) concentrations in young adult and adult rats. As well, AIE significantly blunted the alcohol challenge-induced arginine vasopressin (Avp) mRNA expression in the paraventricular nucleus (PVN) of the hypothalamus of adult rats. Results of the present study are similar to what we have previously shown, that these changes in PVN responsiveness may result from AIE-induced alterations in adrenergic neurons in brain stem regions C1-C3 known to project to the PVN. AIE elevated the number of colocalized c-fos/phenylethanolamine N-methyltransferase (PNMT)-positive cell bodies in the C1 region of adult rats. Together, these data suggest that AIE exposure produces alterations in male HPA axis responsiveness to administration of an acute alcohol challenge that may be long-lasting.

Indexed as

AnimalsArginine VasopressinBrainCentral Nervous System DepressantsCorticosteroneDisease Models, AnimalEthanolMalePhenylethanolamine N-MethyltransferaseProto-Oncogene Proteins c-fosRats, Sprague-DawleyRNA, MessengerStress, PsychologicalArginine VasopressinCentral Nervous System DepressantsCorticosteroneEthanolPhenylethanolamine N-MethyltransferaseProto-Oncogene Proteins c-fosRNA, MessengeralcoholAvpcorticosteroneCrfPNMT

Identifiers

PMID27687801
PMCPMC5354126
OpenAlexW2527454464

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.