Evidence map›Paper›PMID 31421087›Full record

ArticleEuropean journal of pharmacology2019

Chronic memantine decreases nicotine self-administration in rats.

Edward D Levin, Corinne Wells, Leah Yao, Wendi Guo, Anica Nangia, Sarah Howard, Erica Pippen, Andrew B Hawkey, Jed E Rose, Amir H Rezvani

Open access · greenAbstract read
In one paragraph

Article in European journal of pharmacology, 2019. 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
0.1field-weighted citation impact, top 52% 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. Trial
  2. Review
  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

10 authors at 2 institutions in 1 country.

Edward D LevinDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States. Electronic address: edlevin@duke.edu.
Corinne WellsDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Leah YaoDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Wendi GuoDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Anica NangiaDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Sarah HowardDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Erica PippenDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Andrew B HawkeyDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Jed E RoseDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Amir H RezvaniDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, United States.
Duke Medical Center · USDuke University Hospital · US

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

Neurobehavioral bases of tobacco addiction and nicotine reinforcement are complex, involving more than only nicotinic cholinergic or dopaminergic systems. Memantine is an NMDA glutamate antagonist used to improve cognitive function in people with Alzheimer's disease. Glutamate may be an important component of the reinforcing effects of nicotine, so memantine was evaluated as a potential smoking cessation aid. Two studies were conducted with adult female rats, one testing acute effects of memantine over a range of doses for changing nicotine self-administration and the other testing the chronic effects of memantine to reduce nicotine self-administration. Acute memantine injections slightly, but significantly, increased nicotine self-administration in a dose-related manner. In contrast, chronic memantine treatment significantly reduced nicotine self-administration. During the first day of memantine administration in the chronic study, nicotine self-administration was significantly elevated replicating the acute study. Starting in the second week of treatment there was a significant reduction of nicotine self-administration relative to controls. This was seen because memantine treatment prevented the increase in nicotine self-administration shown by controls. There even continued to be a memantine-induced lowered nicotine self-administration during the week after the cessation of memantine treatment. Memantine or other drugs affecting NMDA glutamate receptors may be useful aids to smoking cessation. Full efficacy for reducing nicotine self-administration was seen as the NMDA drug treatment is given chronically. Importantly, the effect persisted even after treatment is ended, indicating the high potential for NMDA glutamate receptors to impact nicotine addiction.

Indexed as

AnimalsDose-Response Relationship, DrugFemaleMemantineNicotineRatsRats, Sprague-DawleySelf AdministrationTime FactorsTobacco Use DisorderMemantineNicotineAcuteChronicMemantineNicotine self-administrationNMDA glutamate receptors

Identifiers

PMID31421087
PMCPMC6732003
OpenAlexW2968750357

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.