Evidence map›Paper›PMID 32588079›Full record

ArticlePsychopharmacology2020

Noradrenergic tone mediates marble burying behavior after chronic stress and ethanol.

Carolina R den Hartog, Katrina L Blandino, McKenzie L Nash, Emily R Sjogren, Michael A Grampetro, David E Moorman, Elena M Vazey

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Carolina R den HartogDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
Katrina L BlandinoDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
McKenzie L NashDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
Emily R SjogrenDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
Michael A GrampetroDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
David E MoormanDepartment of Psychological and Brain Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Elena M VazeyDepartment of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA. evazey@umass.edu.ORCID http://orcid.org/0000-0003-3311-9414
University of Massachusetts Amherst · US

Funding

4/8: INIA Stress and Chronic Alcohol Interactions: Impact of stress mediated locus coeruleus dysregulation on cognitive control and excessive drinkingU01AA025481 · NIAAA · UNIVERSITY OF MASSACHUSETTS AMHERST · PI DAVID E MOORMAN, Elena Vazey · 2017 to 2026
$4.2M
Orbitofrontal coding of alcohol preference and compulsive drinkingR21AA024571 · NIAAA · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MOORMAN, DAVID E · 2016 to 2017
$419k
Brain and Behavior Research Foundation NARSAD Young INvestigatorNIAAA NIH HHS R21 AA024571NIAAA NIH HHS R21AA024571NIAAA NIH HHS U01 AA025481NIAAA NIH HHS U01AA025481
6 · The paper itself

Abstract

rationaleStress plays a major role in the development of alcohol use disorder (AUD)-a history of chronic stress contributes to alcohol misuse, and withdrawal from alcohol elevates stress, perpetuating cycles of problematic drinking. Recent studies have shown that, in male mice, repeated chronic intermittent ethanol (CIE) and stress elevates alcohol use above either manipulation alone and impacts cognitive functions such as behavioral flexibility.

objectiveHere, we investigated the impact of CIE and stress on anxiety in both sexes, and whether the norepinephrine (NE) system via locus coeruleus, which is implicated in both stress and alcohol motivation, is involved.

resultsMale and female mice received multiple cycles of CIE and/or repeated forced swim stress (FSS), producing elevated drinking in both sexes. CIE/FSS treatment increased anxiety, which was blocked by treatment with the α1-AR inverse agonist prazosin. In contrast, administration of the corticotropin releasing factor receptor antagonist CP376395 into locus coeruleus did not reduce CIE/FSS-elevated anxiety. We also observed sex differences in behavioral responses to a history of CIE or FSS alone as well as differential behavioral consequences of prazosin treatment.

conclusionsThese data indicate that NE contributes to the development of anxiety following a history of alcohol and/or stress, and that the influence of both treatment history and NE signaling is sex dependent. These results argue for further investigation of the NE system in relation to disrupted behavior following chronic alcohol and stress, and support the assertion that treatments may differ across sex based on differential neural system engagement.

Indexed as

Adrenergic alpha-1 Receptor AntagonistsAlcohol DrinkingAnimalsAnxietyEthanolFemaleLocus CoeruleusMaleMiceNorepinephrinePrazosinReceptors, Corticotropin-Releasing HormoneSex CharacteristicsAdrenergic alpha-1 Receptor AntagonistsEthanolNorepinephrinePrazosinReceptors, Corticotropin-Releasing HormoneAlcoholAnxietyCRFLocus coeruleusNoradrenalinePrazosinSex differences

Identifiers

PMID32588079
PMCPMC7529922
OpenAlexW3037055231

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.