Evidence map›Paper›PMID 32594187›Full record

ArticlePsychopharmacology2020

Nicotine treatment buffers negative behavioral consequences induced by exposure to physical and emotional stress in adolescent male mice.

Lyonna F Parise, Omar K Sial, Brandon L Warren, Carley R Sattler, Jacqueline C Duperrouzel, Eric M Parise, Carlos A Bolaños-Guzmán

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 51% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

7 authors at 4 institutions in 1 country.

Lyonna F PariseDepartment of Psychological and Brain Sciences, Texas A&M University, 4325 TAMU, College Station, TX, 77843, USA.
Omar K SialDepartment of Psychological and Brain Sciences, Texas A&M University, 4325 TAMU, College Station, TX, 77843, USA.
Brandon L WarrenDepartment of Pharmacodynamics, Department of Pharmacy, University of Florida, 1345 Center Drive, Gainesville, FL, 32610, USA.
Carley R SattlerDepartment of Psychological and Brain Sciences, Texas A&M University, 4325 TAMU, College Station, TX, 77843, USA.
Jacqueline C DuperrouzelDepartment of Psychology, Florida International University, 11200 S.W. 8th St., Miami, FL, 33199, USA.
Eric M PariseFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai. 1 Gustave L. Levy Place, New York, NY, 10029, USA.
Carlos A Bolaños-GuzmánDepartment of Psychological and Brain Sciences, Texas A&M University, 4325 TAMU, College Station, TX, 77843, USA. bolanos@tamu.edu.ORCID http://orcid.org/0000-0003-0655-703X
Texas A&M University · USAllen Institute for Brain Science · USAmerican Association of Colleges of Pharmacy · USFlorida International University · US

Funding

Neuronal ensembles in extinction of cocaine seeking.R00DA042102 · NIDA · UNIVERSITY OF FLORIDA · PI WARREN, BRANDON L · 2019 to 2021
$913k
NIDA NIH HHS R00 DA042102
6 · The paper itself

Abstract

Early life stress influences adult psychopathology and is associated with an increase in the propensity for drug use/seeking throughout the lifespan. Animal models corroborate that stress exposure exacerbates maladaptive reactivity to stressful stimuli while also shifting the rewarding properties of many drugs of abuse, including nicotine (NIC), a stimulant commonly misused by adolescents. Interestingly, NIC treatment can also normalize some stress-induced behavioral deficits in adult rodents; however, little is known about NIC's therapeutic efficacy following stress experienced during adolescence. The goal of the following experiments was to elucidate NIC's ability to buffer the negative consequences of stress exposure, and to further assess behavioral responsivity while on the drug. Given that stress often occurs in both physical and non-physical forms, we employed the vicarious social defeat stress (VSDS) model which allows for investigation of both physical (PS) and emotional stress (ES) exposure. After 10 days, exposure to PS and ES decreased interaction with a social target in the social interaction test (SIT), confirming social avoidance. Groups were further divided and given NIC (0.0 or 160 mg/L) in their drinking water. After 1 month of NIC consumption, the mice were exposed to the SIT, elevated plus maze (EPM), and the forced swim test (FST), respectively. NIC-treated mice showed a reversal of stress-induced deficits in the EPM and FST. Surprisingly, the mice did not show improvement in the SIT regardless of treatment condition. Together, these data confirm NIC's ability to normalize some stress-induced behavioral deficits; however, NIC's effects on social behavior need further investigation.

Indexed as

Psychological DistressSocial BehaviorAge FactorsAnimalsMaleMiceMice, Inbred C57BLNicotineNicotinic AgonistsStress, PhysiologicalStress, PsychologicalTreatment OutcomeNicotineNicotinic AgonistsAdolescenceNicotineStressVicarious social defeat sress (VSDS)

Identifiers

PMID32594187
PMCPMC7819755
OpenAlexW3037925154

What OpenQuestion holds

Textmetadata
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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.