Evidence map›Paper›PMID 30481568›Full record

ArticleNeuroscience2019

Chronic Intermittent Ethanol Exposure Selectively Increases Synaptic Excitability in the Ventral Domain of the Rat Hippocampus.

Sarah E Ewin, James W Morgan, Farr Niere, Nate P McMullen, Samuel H Barth, Antoine G Almonte, Kimberly F Raab-Graham, Jeffrey L Weiner

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Epigenetic regulation ofFrontiers in psychiatry · 2025
    Article
  11. Synaptic Effects Induced by Alcohol.Current topics in behavioral neurosciences · 2025
    Review
  12. Article
  13. Article
  14. Article
  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

8 authors at 1 institution in 1 country.

Sarah E EwinDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
James W MorganDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Farr NiereDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Nate P McMullenDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Samuel H BarthDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Antoine G AlmonteDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Kimberly F Raab-GrahamDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Jeffrey L WeinerDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: jweiner@wakehealth.edu.
Wake Forest University · US

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jeffrey L. Weiner · 2018 to 2026
$16.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
Synaptic Correlates of Vulnerability and Resilience to Alcohol Use DisordersR37AA017531 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2014 to 2023
$3.5M
Synaptic Correlates of Vulnerability and Resilience to Alcohol Use DisorderR01AA017531 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jeffrey L. Weiner · 2009 to 2026
$2.1M
Neural Substrates of Comorbid Alcohol Use Disorder and Post-Traumatic Stress DisorderR01AA026551 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2017 to 2021
$1.9M
The Neurobiology of Drug AbuseT32DA041349 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SARA RAULERSON JONES · 2017 to 2026
$1.8M
The role of the BLA-ventral hippocampal circuit in ethanol withdrawal-related behaviorsR21AA026455 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMONTE, ANTOINE GABRIEL, WEINER, JEFFREY L. · 2018 to 2019
$407k
Effects of Isolation Rearing on Dopamine Release and ReuptakeF31AA020439 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI YORGASON, JORDAN THOMAS · 2011 to 2013
$92k
Dissecting the contributions of the basolateral amygdala - nucleus accumbens circuit in the addiction-vulnerable phenotype engendered by chronic early life stressF31AA025819 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI EWIN, SARAH · 2017 to 2018
$83k
NIAAA NIH HHS F31 AA020439NIAAA NIH HHS F31 AA025819NIAAA NIH HHS P50 AA026117NIAAA NIH HHS R01 AA017531NIAAA NIH HHS R01 AA026551NIAAA NIH HHS R21 AA026455NIAAA NIH HHS R37 AA017531NIAAA NIH HHS T32 AA007565NIDA NIH HHS T32 DA041349NIH HHS AA17531NIH HHS AA25819NIH HHS AA26117NIH HHS AA26455NIH HHS AA26551NIH HHS AA7565
6 · The paper itself

Abstract

Many studies have implicated hippocampal dysregulation in the pathophysiology of alcohol use disorder (AUD). However, over the past twenty years, a growing body of evidence has revealed distinct functional roles of the dorsal (dHC) and ventral (vHC) hippocampal subregions, with the dHC being primarily involved in spatial learning and memory and the vHC regulating anxiety- and depressive-like behaviors. Notably, to our knowledge, no rodent studies have examined the effects of chronic ethanol exposure on synaptic transmission along the dorsal/ventral axis. To that end, we examined the effects of the chronic intermittent ethanol vapor exposure (CIE) model of AUD on dHC and vHC synaptic excitability. Adult male Long-Evans rats were exposed to CIE or AIR for 10 days (12 h/day; targeting blood ethanol levels of 175-225 mg%) and recordings were made 24 h into withdrawal. As expected, this protocol increased anxiety-like behaviors on the elevated plus-maze and successive alleys test. Extracellular recordings revealed marked CIE-associated increases in synaptic excitation in the CA1 region that were exclusively restricted to the ventral domain of the hippocampus. Western blot analysis of synaptoneurosomal fractions revealed that the expression of two proteins that regulate synaptic strength, GluA2 and SK2, were dysregulated in the vHC, but not the dHC, following CIE. Together, these findings suggest that the ventral CA1 region may be particularly sensitive to the maladaptive effects of chronic ethanol exposure and provide new insight into some of the neural substrates that may contribute to the negative affective state that develops during withdrawal.

Indexed as

Alcohol-Related DisordersAnimalsCentral Nervous System DepressantsDisease Models, AnimalEthanolGene ExpressionGerminal Center KinasesHippocampusHippo KinasesMaleProtein Serine-Threonine KinasesRats, Long-EvansReceptors, N-Methyl-D-AspartateSynapsesSynaptic TransmissionCentral Nervous System DepressantsEthanolGerminal Center KinasesHippo KinasesProtein Serine-Threonine KinasesReceptors, N-Methyl-D-AspartateSlk protein, ratanxietychronic intermittent ethanoldorsal hippocampusSK Calcium-activated potassium channelsventral hippocampuswithdrawal

Identifiers

PMID30481568
PMCPMC6658135
OpenAlexW2951460389

What OpenQuestion holds

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Registered trials

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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.