Evidence map›Paper›PMID 32246985›Full record

ArticlePharmacology, biochemistry, and behavior2020

Dextromethorphan and bupropion reduces high level remifentanil self-administration in rats.

Graham Blair, Corinne Wells, Ashley Ko, John Modarres, Caroline Pace, James M Davis, Amir H Rezvani, Jed E Rose, Edward D Levin

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Graham BlairDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Corinne WellsDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Ashley KoDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
John ModarresDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Caroline PaceDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
James M DavisDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA; Duke Cancer Institute, Durham, NC, USA.
Amir H RezvaniDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Jed E RoseDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA; Duke Cancer Institute, Durham, NC, USA.
Edward D LevinDepartment of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA; Duke Cancer Institute, Durham, NC, USA. Electronic address: edlevin@duke.edu.
Duke University · USDuke Cancer Institute

Funding

Recruitment CoreP50DA027840 · NIDA · DUKE UNIVERSITY · PI DAVIS, JAMES M · 2010 to 2019
$14.9M
NIDA NIH HHS P50 DA027840
6 · The paper itself

Abstract

Opiate addiction has risen substantially during the past decade. New treatments to combat opiate addiction are sorely needed. The current study was conducted to determine the acute individual and interactive effects of bupropion and dextromethorphan in a rat model of opiate self-administration using the short-acting synthetic opioid remifentanil. Both of these drugs have been found to reduce self-administration of nicotine. Bupropion and dextromethorphan and their combination had differential effects depending on whether the rats showed higher or lower baseline remifentanil self-administration. The rats with higher initial remifentanil self-administration showed a significant decrease in remifentanil self-administration with bupropion or dextromethorphan treatment, compared to the vehicle control condition. This decrease in self-remifentanil administration was most pronounced when combination of the higher doses of bupropion and dextromethorphan were administered. In contrast, the rats with lower baseline remifentanil self-administration showed the opposite effect of drug treatment with an increase in remifentanil self-administration with bupropion treatment compared to the vehicle control condition. Dextromethorphan had no significant effect inthis group. This study shows that combination bupropion and dextromethorphan affects remifentanil self-administration in a complex fashion with differential effects on low and high baseline responders. In subjects with high baseline remifentanil self-administration, bupropion and dextromethorphan treatment significantly reduced self-administration, whereas in subjects with low baseline remifentanil self-administration, bupropion increased remifentanil self-administration and dextromethorphan had no discernible effect. This finding suggests that combination bupropion-dextromethorphan should be tested in humans, with a focus on treating people with high-level opiate use.

Indexed as

Analgesics, OpioidAnimalsBehavior, AnimalBupropionDextromethorphanDisease Models, AnimalDose-Response Relationship, DrugDrug Therapy, CombinationFemaleLocomotionMotivationOpioid-Related DisordersRatsRats, Sprague-DawleyRemifentanilSelf AdministrationAnalgesics, OpioidBupropionDextromethorphanRemifentanilBupropionDextromethorphanOpioidsRatsRemifentanilSelf-administration

Identifiers

PMID32246985
PMCPMC7291818
OpenAlexW3014347325

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.