Evidence map›Paper›PMID 32750464›Full record

ArticleBehavioural brain research2020

Sex differences in the effects of a combined behavioral and pharmacological treatment strategy for cocaine relapse prevention in an animal model of cue exposure therapy.

Kathleen M Kantak, Jamie M Gauthier, Elon Mathieson, Eudokia Knyazhanskaya, Pedro Rodriguez-Echemendia, Heng-Ye Man

Open access · greenAbstract read
In one paragraph

Article in Behavioural brain research, 2020. 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
0.1field-weighted citation impact, top 60% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  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

6 authors at 1 institution in 1 country.

Kathleen M KantakDepartment of Psychological and Brain Sciences, Boston University, Boston, USA; Center for Systems Neuroscience, Boston University, Boston, USA. Electronic address: kkantak@bu.edu.
Jamie M GauthierDepartment of Psychological and Brain Sciences, Boston University, Boston, USA.
Elon MathiesonDepartment of Psychological and Brain Sciences, Boston University, Boston, USA.
Eudokia KnyazhanskayaDepartment of Psychological and Brain Sciences, Boston University, Boston, USA.
Pedro Rodriguez-EchemendiaDepartment of Psychological and Brain Sciences, Boston University, Boston, USA.
Heng-Ye ManDepartment of Biology, Boston University, Boston, USA; Center for Systems Neuroscience, Boston University, Boston, USA.
Boston University · US

Funding

Mechanisms of Extinction Memory Enhancement for Cocaine Addiction TreatmentR01DA043454 · NIDA · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KANTAK, KATHLEEN M. · 2017 to 2021
$2.6M
NIDA NIH HHS R01 DA043454
6 · The paper itself

Abstract

Brief interventions of environmental enrichment (EE) or the glycine transporter-1 inhibitor Org24598 administered with cocaine-cue extinction training were shown previously to inhibit reacquisition of cocaine self-administration in male rats trained to self-administer a moderate 0.3 mg/kg dose of cocaine. Determining how EE and Org24598 synergize in combination in an animal model of cue exposure therapy is novel. Important changes made in this investigation were increasing the cocaine training dose to 1.0 mg/kg and determining sex differences. Adult male and female rats self-administering 1.0 mg/kg cocaine for 35-40 daily sessions exhibited an addiction-like phenotype under a second-order schedule of cocaine delivery and cue presentation. Rats next underwent 6 weekly extinction training sessions for which treatments consisted of EE or NoEE and Vehicle or Org24598 (3.0 mg/kg in males; 3.0 or 7.5 mg/kg in females). Rats then were tested for reacquisition of cocaine self-administration for 15 daily sessions. In males, the combined EE +3.0 mg/kg Org24598 treatment facilitated extinction learning and inhibited reacquisition of cocaine self-administration to a greater extent than no treatment and to individual EE or 3.0 mg/kg Org24598 treatments. In females, EE +7.5 mg/kg Org24598 facilitated extinction learning, but did not inhibit reacquisition of cocaine self-administration. Thus, there were sex differences in the ability of EE + Org24598 administered in conjunction with extinction training to inhibit cocaine relapse in rats exhibiting an addiction-like phenotype. These findings suggest that this multimodal treatment approach might be a feasible option during cue exposure therapy in cocaine-dependent men, but not women.

Indexed as

AnimalsBehavior, AddictiveBehavior TherapyCocaineCocaine-Related DisordersConditioning, OperantCuesDisease Models, AnimalExtinction, PsychologicalFemaleImplosive TherapyLearningMaleRatsRats, WistarSecondary PreventionCocaineCocaineCue extinctionEnvironmental enrichmentOrg24598RelapseSex differences

Identifiers

PMID32750464
PMCPMC7492466
OpenAlexW3046413993

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.