Evidence map›Paper›PMID 35102423›Full record

ArticlePsychopharmacology2022

N

Lee Peyton, Brandon Emanuel León, Hesham Essa, Yijuang Chern, Doo-Sup Choi

Abstract read
In one paragraph

Article in Psychopharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Lee PeytonDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN, 55905, USA.
Brandon Emanuel LeónRegenerative Sciences Program, Center for Regenerative Medicine, Mayo Clinic College of Medicine Rochester, Rochester, MN, 55905, USA.
Hesham EssaDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN, 55905, USA.
Yijuang ChernInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Doo-Sup ChoiDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN, 55905, USA. choids@mayo.edu.ORCID http://orcid.org/0000-0002-6796-9938

Funding

Alcohol and Adenosine-Mediated Glutamate Signaling in Neuro-Glial InteractionR01AA018779 · NIAAA · MAYO CLINIC ROCHESTER · PI CHOI, DOO-SUP · 2009 to 2019
$3.8M
Chronic Alcohol Exposure and Pathophysiology of Alzheimer's Disease.R01AG072898 · NIA · MAYO CLINIC ROCHESTER · PI CHOI, DOO-SUP, TRUSHINA, EUGENIA · 2020 to 2024
$2.0M
Astrocyte-Neuron Interaction in the Dorsal Striatum and Ethanol-Seeking Behaviors Diversity supplement - Matthew LopezR01AA029258 · NIAAA · MAYO CLINIC ROCHESTER · PI CHOI, DOO-SUP · 2021 to 2025
$1.8M
Neural Basis of Ethanol Withdrawal-Induced Sleep DisturbanceR21AA028968 · NIAAA · MAYO CLINIC ROCHESTER · PI CHOI, DOO-SUP · 2021 to 2022
$417k
NIAAA NIH HHS AA018779NIAAA NIH HHS AA029258NIAAA NIH HHS R01 AA018779NIAAA NIH HHS R01 AA029258NIAAA NIH HHS R21 AA028968NIA NIH HHS AG072898NIA NIH HHS R01 AG072898
6 · The paper itself

Abstract

rationaleWithdrawal from chronic alcohol exposure produces various physical and mental withdrawal symptoms. Activation of adenosine receptors is known to inhibit withdrawal-induced excitation. However, limited studies investigate how adenosine analogs may prove helpful tools to alleviate alcohol withdrawal-related affective behaviors.

objectivesThis study aimed to investigate the effects of J4 compared with saline using the mice vapor or voluntary ethanol drinking model on behavioral endpoints representing ethanol-withdrawal negative emotionality commonly observed during abstinence from chronic alcohol use.

methodsWe subjected C57BL/6 J mice to chronic intermittent ethanol (CIE) exposure schedule to investigate how 72-h withdrawal from alcohol alters affective-like behavior. Next, we determined how treatment with J4, a second-generation adenosine analog, influenced affective behaviors produced by alcohol withdrawal. Finally, we determined how J4 treatment alters voluntary ethanol drinking using the two-bottle-choice drinking paradigm.

resultsOur results show that 72-h withdrawal from chronic intermittent ethanol exposure produces limited affective-like disturbances in male C57BL/6 J mice exposed to 4 cycles ethanol vapor. Most importantly, J4 treatment irrespective of ethanol exposure decreases innate anxiety-like behavior in mice.

conclusionsWithdrawal from chronic intermittent ethanol exposure and subsequent behavioral testing 72 h later produces minimal affective-like behavior. J4 treatment did however reduce marble-burying behavior and increased time spent in open arms of the elevated plus maze, suggesting J4 may be useful as a general anxiolytic.

Indexed as

AlcoholismSubstance Withdrawal SyndromeAdenosineAlcohol DrinkingAnimalsAnxietyMaleMiceMice, Inbred C57BLAdenosineAdenosineElevated-plus mazeJ4Marble-buryingTwo-bottle choice

Identifiers

PMID35102423
PMCPMC9063204

What OpenQuestion holds

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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.